Neurons: Structure and Function - Study Notes PDF
Document Details

Uploaded by BullishStrontium
Jefferson Community College
Tags
Summary
This document provides an overview of neurons, which are the building blocks of the nervous system. It describes neuron structure, including the soma, dendrites, axon, and terminal buttons and explains the function of these parts in neuronal communication. It also introduces key concepts like neurotransmitters, synapses, and the myelin sheath, providing a foundation for understanding the nervous system.
Full Transcript
Neurons Psychologists striving to understand the human mind may study the **nervous system**. Learning how the cells and organs (like the brain) function, help us understand the biological basis behind human psychology. The nervous system is composed of two basic cell types: glial cells (also known...
Neurons Psychologists striving to understand the human mind may study the **nervous system**. Learning how the cells and organs (like the brain) function, help us understand the biological basis behind human psychology. The nervous system is composed of two basic cell types: glial cells (also known as glia) and neurons. **Glial cells**, which outnumber neurons ten to one, are traditionally thought to play a supportive role to neurons, both physically and metabolically. Glial cells provide scaffolding on which the nervous system is built, help neurons line up closely with each other to allow neuronal communication, provide insulation to neurons, transport nutrients and waste products, and mediate immune responses. **Neurons**, on the other hand, serve as interconnected information processors that are essential for all of the tasks of the nervous system. This section briefly describes the structure and function of neurons. Neuron Structure Neurons are the central building blocks of the nervous system, 100 billion strong at birth. Like all cells, neurons consist of several different parts, each serving a specialized function. A neuron's outer surface is made up of a **semipermeable membrane**. This membrane allows smaller molecules and molecules without an electrical charge to pass through it, while stopping larger or highly charged molecules. An illustration shows a neuron with labeled parts for the cell membrane, dendrite, cell body, axon, and terminal buttons. A myelin sheath covers part of the neuron.**Figure 1. This illustration shows a prototypical neuron, which is being myelinated.** The nucleus of the neuron is located in the soma, or cell body. The **soma** has branching extensions known as **dendrites**. The neuron is a small information processor, and dendrites serve as input sites where signals are received from other neurons. These signals are transmitted electrically across the soma and down a major extension from the soma known as the **axon**, which ends at multiple **terminal buttons**. The terminal buttons contain **synaptic vesicles** that house **neurotransmitters**, the chemical messengers of the nervous system.\ \ Axons range in length from a fraction of an inch to several feet. In some axons, glial cells form a fatty substance known as the **myelin sheath**, which coats the axon and acts as an insulator, increasing the speed at which the signal travels. The myelin sheath is crucial for the normal operation of the neurons within the nervous system: the loss of the insulation it provides can be detrimental to normal function. To understand how this works, let's consider an example. Multiple sclerosis (MS), an autoimmune disorder, involves a large-scale loss of the myelin sheath on axons throughout the nervous system. The resulting interference in the electrical signal prevents the quick transmittal of information by neurons and can lead to a number of symptoms, such as dizziness, fatigue, loss of motor control, and sexual dysfunction. While some treatments may help to modify the course of the disease and manage certain symptoms, there is currently no known cure for multiple sclerosis.\ \ In healthy individuals, the neuronal signal moves rapidly down the axon to the terminal buttons, where synaptic vesicles release neurotransmitters into the synapse. The **synapse** is a very small space between two neurons and is an important site where communication between neurons occurs. Once neurotransmitters are released into the synapse, they travel across the small space and bind with corresponding receptors on the dendrite of an adjacent neuron. **Receptors**, proteins on the cell surface where neurotransmitters attach, vary in shape, with different shapes "matching" different neurotransmitters. How does a neurotransmitter "know" which receptor to bind to? The neurotransmitter and the receptor have what is referred to as a lock-and-key relationship---specific neurotransmitters fit specific receptors similar to how a key fits a lock. The neurotransmitter binds to any receptor that it fits. Now that we have learned about the basic structures of the neuron and the role that these structures play in neuronal communication, let's take a closer look at the signal itself---how it moves through the neuron and then jumps to the next neuron, where the process is repeated. We begin at the neuronal membrane. The **neuron** exists in a fluid environment---it is surrounded by extracellular fluid and contains intracellular fluid (i.e., cytoplasm). The neuronal membrane keeps these two fluids separate---a critical role because the electrical signal that passes through the neuron depends on the intra- and extracellular fluids being electrically different. This difference in charge across the membrane, called the **membrane potential**, provides energy for the signal. The electrical charge of the fluids is caused by charged molecules (ions) dissolved in the fluid. The semipermeable nature of the neuronal membrane somewhat restricts the movement of these charged molecules, and, as a result, some of the charged particles tend to become more concentrated either inside or outside the cell. Between signals, the neuron membrane's potential is held in a state of readiness, called the **resting potential**. Like a rubber band stretched out and waiting to spring into action, ions line up on either side of the cell membrane, ready to rush across the membrane when the neuron goes active and the membrane opens its gates (i.e., a sodium-potassium pump that allows movement of ions across the membrane). Ions in high-concentration areas are ready to move to low-concentration areas, and positive ions are ready to move to areas with a negative charge. In the resting state, sodium (Na^+^) is at higher concentrations outside the cell, so it will tend to move into the cell. Potassium (K^+^), on the other hand, is more concentrated inside the cell, and will tend to move out of the cell (Figure 3). In addition, the inside of the cell is slightly negatively charged compared to the outside. This provides an additional force on sodium, causing it to move into the cell. From this resting potential state, the neuron receives a signal and its state changes abruptly (Figure 4). When a neuron receives signals at the dendrites---due to neurotransmitters from an adjacent neuron binding to its receptors---small pores, or gates, open on the neuronal membrane, allowing Na^+^ ions, propelled by both charge and concentration differences, to move into the cell. With this influx of positive ions, the internal charge of the cell becomes more positive. If that charge reaches a certain level, called the **threshold of excitation**, the neuron becomes active and the action potential begins. This process of when the cell\'s charge becomes positive, or less negative, is called **depolarization**.\ \ Many additional pores open, causing a massive influx of Na^+^ ions and a huge positive spike in the membrane potential, the peak action potential. At the peak of the spike, the sodium gates close and the potassium gates open. As positively charged potassium ions leave, the cell quickly begins repolarization. At first, it **hyperpolarizes**, becoming slightly more negative than the resting potential, and then it levels off, returning to the resting potential. **Figure 4. During the action potential, the electrical charge across the membrane changes dramatically.** This positive spike constitutes the **action potential**: the electrical signal that typically moves from the cell body down the axon to the axon terminals. The electrical signal moves down the axon like a wave; at each point, some of the sodium ions that enter the cell diffuse to the next section of the axon, raising the charge past the threshold of excitation and triggering a new influx of sodium ions. The action potential moves all the way down the axon to the terminal buttons. The action potential is an **all-or-none** phenomenon. In simple terms, this means that an incoming signal from another neuron is either sufficient or insufficient to reach the threshold of excitation. There is no in-between, and there is no turning off an action potential once it starts. Think of it like sending an email or a text message. You can think about sending it all you want, but the message is not sent until you hit the send button. Furthermore, once you send the message, there is no stopping it.\ \ Because it is all or none, the **action potential** is recreated, or propagated, at its full strength at every point along the axon. Much like the lit fuse of a firecracker, it does not fade away as it travels down the axon. It is this all-or-none property that explains the fact that your brain perceives an injury to a distant body part like your toe as equally painful as one to your nose.\ \ As noted earlier, when the action potential arrives at the terminal button, the synaptic vesicles release their neurotransmitters into the **synapse**. The neurotransmitters travel across the synapse and bind to receptors on the dendrites of the adjacent neuron, and the process repeats itself in the new neuron (assuming the signal is sufficiently strong to trigger an action potential). Once the signal is delivered, excess neurotransmitters in the synapse drift away, are broken down into inactive fragments, or are reabsorbed in a process known as reuptake. **Reuptake** involves the neurotransmitter being pumped back into the neuron that released it, in order to clear the synapse (Figure 5). Clearing the synapse serves both to provide a clear "on" and "off" state between signals and to regulate the production of neurotransmitter (full synaptic vesicles provide signals that no additional neurotransmitters need to be produced). The synaptic space between two neurons is shown. Some neurotransmitters that have been released into the synapse are attaching to receptors while others undergo reuptake into the axon terminal. Neuronal communication is often referred to as an electrochemical event. The movement of the action potential down the length of the axon is an electrical event, and movement of the neurotransmitter across the synaptic space represents the chemical portion of the process. Neurotransmitters and Drugs There are several different types of **neurotransmitters** released by different neurons, and we can speak in broad terms about the kinds of functions associated with different neurotransmitters (Table 1). Much of what psychologists know about the functions of neurotransmitters comes from research on the effects of drugs in psychological disorders. Psychologists who take a **biological perspective** and focus on the physiological causes of behavior assert that psychological disorders like depression and schizophrenia are associated with imbalances in one or more neurotransmitter systems. In this perspective, **psychotropic medications** can help improve the symptoms associated with these disorders. Psychotropic medications are drugs that treat psychiatric symptoms by restoring neurotransmitter balance. Table 1. Major Neurotransmitters and How They Affect Behavior --------------------------------------------------------------- ------------------------------ ----------------------------------------- **Neurotransmitter** **Involved in** **Potential Effect on Behavior** Acetylcholine Muscle action, memory Increased arousal, enhanced cognition Beta-endorphin Pain, pleasure Decreased anxiety, decreased tension Dopamine Mood, sleep, learning Increased pleasure, suppressed appetite Gamma-aminobutyric acid (GABA) Brain function, sleep Decreased anxiety, decreased tension Glutamate Memory, learning Increased learning, enhanced memory Norepinephrine Heart, intestines, alertness Increased arousal, suppressed appetite Serotonin Mood, sleep Modulated mood, suppressed appetite Psychoactive drugs can act as agonists or antagonists for a given neurotransmitter system. **Agonists** are chemicals that mimic a neurotransmitter at the receptor site and, thus, strengthen its effects. An **antagonist,** on the other hand, blocks or impedes the normal activity of a neurotransmitter at the receptor. Agonist and antagonist drugs are prescribed to correct the specific neurotransmitter imbalances underlying a person's condition. For example, Parkinson\'s disease, a progressive nervous system disorder, is associated with low levels of dopamine. Therefore dopamine agonists, which mimic the effects of dopamine by binding to dopamine receptors, are one treatment strategy.\ \ Certain symptoms of schizophrenia are associated with overactive dopamine neurotransmission. The antipsychotics used to treat these symptoms are antagonists for dopamine---they block dopamine's effects by binding its receptors without activating them. Thus, they prevent dopamine released by one neuron from signaling information to adjacent neurons.\ \ In contrast to agonists and antagonists, which both operate by binding to receptor sites, reuptake inhibitors prevent unused neurotransmitters from being transported back to the neuron. This leaves more neurotransmitters in the synapse for a longer time, increasing its effects. Depression, which has been consistently linked with reduced serotonin levels, is commonly treated with selective serotonin reuptake inhibitors (SSRIs). By preventing reuptake, SSRIs strengthen the effect of serotonin, giving it more time to interact with serotonin receptors on dendrites. Common SSRIs on the market today include Prozac, Paxil, and Zoloft. The drug LSD is structurally very similar to serotonin, and it affects the same neurons and receptors as serotonin. Psychotropic drugs are not instant solutions for people suffering from psychological disorders. Often, an individual must take a drug for several weeks before seeing improvement, and many psychoactive drugs have significant negative side effects. Furthermore, individuals vary dramatically in how they respond to the drugs. To improve chances for success, it is not uncommon for people receiving pharmacotherapy to undergo psychological and/or behavioral therapies as well. Some research suggests that combining drug therapy with other forms of therapy tends to be more effective than any one treatment alone (for one such example, see March et al., 2007). Glossary **action potential: **electrical signal that moves down the neuron's axon **agonist: **drug that mimics or strengthens the effects of a neurotransmitter **all-or-none: **phenomenon that incoming signal from another neuron is either sufficient or insufficient to reach the threshold of excitation **antagonist: **drug that blocks or impedes the normal activity of a given neurotransmitter **axon: **major extension of the soma **biological perspective: **view that psychological disorders like depression and schizophrenia are associated with imbalances in one or more neurotransmitter systems **dendrite: **branch-like extension of the soma that receives incoming signals from other neurons **depolarization: **when a cell\'s charge becomes positive, or less negative **glial cell: **nervous system cell that provides physical and metabolic support to neurons, including neuronal insulation and communication, and nutrient and waste transport **hyperpolarization: **when a cell\'s charge becomes more negative than its resting potential **membrane potential: **difference in charge across the neuronal membrane **myelin sheath: **fatty substance that insulates axons **neuron: **cells in the nervous system that act as interconnected information processors, which are essential for all of the tasks of the nervous system **neurotransmitter: **chemical messenger of the nervous system **psychotropic medication: **drugs that treat psychiatric symptoms by restoring neurotransmitter balance **receptor: **protein on the cell surface where neurotransmitters attach **resting potential: **the state of readiness of a neuron membrane's potential between signals **reuptake: **neurotransmitter is pumped back into the neuron that released it **semipermeable membrane: **cell membrane that allows smaller molecules or molecules without an electrical charge to pass through it, while stopping larger or highly charged molecules **soma: **cell body **synapse: **small gap between two neurons where communication occurs **synaptic vesicle: **storage site for neurotransmitters **terminal button: **axon terminal containing synaptic vesicles **threshold of excitation: **level of charge in the membrane that causes the neuron to become active The nervous system and the Endocrine system The Central Nervous System and the Peripheral Nervous System The **nervous system** can be divided into two major subdivisions: the **central nervous system (CNS)** and the **peripheral nervous system (PNS)**, shown in Figure 1. The CNS is comprised of the brain and spinal cord; the PNS connects the CNS to the rest of the body. In this section, we focus on the peripheral nervous system; later, we look at the brain and spinal cord. **Figure 1. The nervous system is divided into two major parts: (a) the Central Nervous System and (b) the Peripheral Nervous System.** Peripheral Nervous System The peripheral nervous system is made up of thick bundles of axons, called nerves, carrying messages back and forth between the CNS and the muscles, organs, and senses in the periphery of the body (i.e., everything outside the CNS). The PNS has two major subdivisions: the somatic nervous system and the autonomic nervous system. The **somatic nervous system** is associated with activities traditionally thought of as conscious or voluntary. It is involved in the relay of sensory and motor information to and from the CNS; therefore, it consists of motor neurons and sensory neurons. Motor neurons, carrying instructions from the CNS to the muscles, are efferent fibers (efferent means "moving away from"). Sensory neurons, carrying sensory information to the CNS, are afferent fibers (afferent means "moving toward"). Each nerve is basically a two-way superhighway, containing thousands of axons, both efferent and afferent. The **autonomic nervous system** controls our internal organs and glands and is generally considered to be outside the realm of voluntary control. It can be further subdivided into the sympathetic and parasympathetic divisions (Figure 2). The **sympathetic nervous system** is involved in preparing the body for stress-related activities; the **parasympathetic nervous system** is associated with returning the body to routine, day-to-day operations. The two systems have complementary functions, operating in tandem to maintain the body's homeostasis. **Homeostasis** is a state of equilibrium, in which biological conditions (such as body temperature) are maintained at optimal levels. A diagram of a human body lists the different functions of the sympathetic and parasympathetic nervous system. The parasympathetic system can constrict pupils, stimulate salivation, slow heart rate, constrict bronchi, stimulate digestion, stimulate bile secretion, and cause the bladder to contract. The sympathetic nervous system can dilate pupils, inhibit salivation, increase heart rate, dilate bronchi, inhibit digestion, stimulate the breakdown of glycogen, stimulate secretion of adrenaline and noradrenaline, and inhibit contraction of the bladder.**Figure 2. The sympathetic and parasympathetic divisions of the autonomic nervous system have the opposite effects on various systems.** The sympathetic nervous system is activated when we are faced with stressful or high-arousal situations. The activity of this system was adaptive for our ancestors, increasing their chances of survival. Imagine, for example, that one of our early ancestors, out hunting small game, suddenly disturbs a large bear with her cubs. At that moment, his body undergoes a series of changes---a direct function of sympathetic activation---preparing him to face the threat. His pupils dilate, his heart rate and blood pressure increase, his bladder relaxes, his liver releases glucose, and adrenaline surges into his bloodstream. This constellation of physiological changes, known as the **fight or flight response**, allows the body access to energy reserves and heightened sensory capacity so that it might fight off a threat or run away to safety. While it is clear that such a response would be critical for survival for our ancestors, who lived in a world full of real physical threats, many of the high-arousal situations we face in the modern world are more psychological in nature. For example, think about how you feel when you have to stand up and give a presentation in front of a roomful of people, or right before taking a big test. You are in no real physical danger in those situations, and yet you have evolved to respond to any perceived threat with the fight or flight response. This kind of response is not nearly as adaptive in the modern world; in fact, we suffer negative health consequences when faced constantly with psychological threats that we can neither fight nor flee. Recent research suggests that an increase in susceptibility to heart disease (Chandola, Brunner, & Marmot, 2006) and impaired function of the immune system (Glaser & Kiecolt-Glaser, 2005) are among the many negative consequences of persistent and repeated exposure to stressful situations. Once the threat has been resolved, the parasympathetic nervous system takes over and returns bodily functions to a relaxed state. Our hunter's heart rate and blood pressure return to normal, his pupils constrict, he regains control of his bladder, and the liver begins to store glucose in the form of glycogen for future use. These processes are associated with activation of the parasympathetic nervous system. The Endocrine System The **endocrine system** consists of a series of glands that produce chemical substances known as **hormones** (Figure 3). Like neurotransmitters, hormones are chemical messengers that must bind to a receptor in order to send their signal. However, unlike neurotransmitters, which are released in close proximity to cells with their receptors, hormones are secreted into the bloodstream and travel throughout the body, affecting any cells that contain receptors for them. Thus, whereas neurotransmitters' effects are localized, the effects of hormones are widespread. Also, hormones are slower to take effect, and tend to be longer lasting. **Figure 3. The major glands of the endocrine system are shown.** The study of psychology and the endocrine system is called behavioral endocrinology, which is the scientific study of the interaction between hormones and behavior. This interaction is bidirectional: hormones can influence behavior, and behavior can sometimes influence hormone concentrations. Hormones regulate behaviors such as aggression, mating, and parenting of individuals. Hormones are involved in regulating all sorts of bodily functions, and they are ultimately controlled through interactions between the hypothalamus (in the central nervous system) and the pituitary gland (in the endocrine system). Imbalances in hormones are related to a number of disorders. This section explores some of the major glands that make up the endocrine system and the hormones secreted by these glands. Major Glands The **pituitary gland** descends from the hypothalamus at the base of the brain, and acts in close association with it. The pituitary is often referred to as the "master gland" because its messenger hormones control all the other glands in the endocrine system, although it mostly carries out instructions from the hypothalamus. In addition to messenger hormones, the pituitary also secretes growth hormone, endorphins for pain relief, and a number of key hormones that regulate fluid levels in the body.\ \ Located in the neck, the **thyroid gland** releases hormones that regulate growth, metabolism, and appetite. In hyperthyroidism, or Grave's disease, the thyroid secretes too much of the hormone thyroxine, causing agitation, bulging eyes, and weight loss. In hypothyroidism, reduced hormone levels cause sufferers to experience tiredness, and they often complain of feeling cold. Fortunately, thyroid disorders are often treatable with medications that help reestablish a balance in the hormones secreted by the thyroid.\ \ The **adrenal glands** sit atop our kidneys and secrete hormones involved in the stress response, such as epinephrine (adrenaline) and norepinephrine (noradrenaline). The **pancreas** is an internal organ that secretes hormones that regulate blood sugar levels: insulin and glucagon. These pancreatic hormones are essential for maintaining stable levels of blood sugar throughout the day by lowering blood glucose levels (insulin) or raising them (glucagon). People who suffer from **diabetes** do not produce enough insulin; therefore, they must take medications that stimulate or replace insulin production, and they must closely control the amount of sugars and carbohydrates they consume.\ \ The **gonads** secrete sexual hormones, which are important in reproduction, and mediate both sexual motivation and behavior. The female gonads are the ovaries; the male gonads are the testis. Ovaries secrete estrogens and progesterone, and the testes secrete androgens, such as testosterone. Hormones and Behavior How might behaviors affect hormones? Extensive studies on male zebra finches and their singing (only males finches sing) demonstrate that the hormones testosterone and estradiol affect their singing, but the reciprocal relation also occurs; that is, behavior can affect hormone concentrations. For example, the sight of a territorial intruder may elevate blood testosterone concentrations in resident male birds and thereby stimulate singing or fighting behavior. Similarly, male mice or rhesus monkeys that lose a fight decrease circulating testosterone concentrations for several days or even weeks afterward. Comparable results have also been reported in humans. Testosterone concentrations are affected not only in humans involved in physical combat, but also in those involved in simulated battles. For example, testosterone concentrations were elevated in winners and reduced in losers of regional chess tournaments.\ \ People do not have to be directly involved in a contest to have their hormones affected by the outcome of the contest. Male fans of both the Brazilian and Italian teams were recruited to provide saliva samples to be assayed for testosterone before and after the final game of the World Cup soccer match in 1994. Brazil and Italy were tied going into the final game, but Brazil won on a penalty kick at the last possible moment. The Brazilian fans were elated and the Italian fans were crestfallen. When the samples were assayed, 11 of 12 Brazilian fans who were sampled had increased testosterone concentrations, and 9 of 9 Italian fans had decreased testosterone concentrations, compared with pre-game baseline values (Dabbs, 2000).\ \ In some cases, hormones can be affected by anticipation of behavior. For example, testosterone concentrations also influence sexual motivation and behavior in women. In one study, the interaction between sexual intercourse and testosterone was compared with other activities (cuddling or exercise) in women (van Anders, Hamilton, Schmidt, & Watson, 2007). On three separate occasions, women provided a pre-activity, post-activity, and next-morning saliva sample. After analysis, the women's testosterone was determined to be elevated prior to intercourse as compared to other times. Thus, an anticipatory relationship exists between sexual behavior and testosterone. Testosterone values were higher post-intercourse compared to exercise, suggesting that engaging in sexual behavior may also influence hormone concentrations in women. Glossary **adrenal gland: **sits atop our kidneys and secretes hormones involved in the stress response **autonomic nervous system: **controls our internal organs and glands **central nervous system (CNS): **brain and spinal cord **diabetes: **disease related to insufficient insulin production **endocrine system: **series of glands that produce chemical substances known as hormones **fight or flight response: **activation of the sympathetic division of the autonomic nervous system, allowing access to energy reserves and heightened sensory capacity so that we might fight off a given threat or run away to safety **gonad: **secretes sexual hormones, which are important for successful reproduction, and mediate both sexual motivation and behavior **homeostasis: **state of equilibrium---biological conditions, such as body temperature, are maintained at optimal levels **hormone: **chemical messenger released by endocrine glands **pancreas: **secretes hormones that regulate blood sugar **parasympathetic nervous system: **associated with routine, day-to-day operations of the body **peripheral nervous system (PNS): **connects the brain and spinal cord to the muscles, organs and senses in the periphery of the body **pituitary gland: **secretes a number of key hormones, which regulate fluid levels in the body, and a number of messenger hormones, which direct the activity of other glands in the endocrine system **thyroid: **secretes hormones that regulate growth, metabolism, and appetite **somatic nervous system: **relays sensory and motor information to and from the CNS **sympathetic nervous system: **involved in stress-related activities and functions Parts of the Brain The Central Nervous System The central nervous system (CNS), consists of the brain and the spinal cord. The Brain The brain is a remarkably complex organ comprised of billions of interconnected neurons and glia. It is a bilateral, or two-sided, structure that can be separated into distinct lobes. Each lobe is associated with certain types of functions, but, ultimately, all of the areas of the brain interact with one another to provide the foundation for our thoughts and behaviors. The Spinal Cord It can be said that the spinal cord is what connects the brain to the outside world. Because of it, the brain can act. The spinal cord is like a relay station, but a very smart one. It not only routes messages to and from the brain, but it also has its own system of automatic processes, called reflexes.\ \ The top of the spinal cord merges with the brain stem, where the basic processes of life are controlled, such as breathing and digestion. In the opposite direction, the spinal cord ends just below the ribs---contrary to what we might expect, it does not extend all the way to the base of the spine.\ \ The spinal cord is functionally organized in 30 segments, corresponding with the vertebrae. Each segment is connected to a specific part of the body through the peripheral nervous system. Nerves branch out from the spine at each vertebra. Sensory nerves bring messages in; motor nerves send messages out to the muscles and organs. Messages travel to and from the brain through every segment.\ \ Some sensory messages are immediately acted on by the spinal cord, without any input from the brain. Withdrawal from heat and knee jerk are two examples. When a sensory message meets certain parameters, the spinal cord initiates an automatic reflex. The signal passes from the sensory nerve to a simple processing center, which initiates a motor command. Seconds are saved, because messages don't have to go the brain, be processed, and get sent back. In matters of survival, the spinal reflexes allow the body to react extraordinarily fast.\ \ The spinal cord is protected by bony vertebrae and cushioned in cerebrospinal fluid, but injuries still occur. When the spinal cord is damaged in a particular segment, all lower segments are cut off from the brain, causing paralysis. Therefore, the lower on the spine damage is, the fewer functions an injured individual loses. The Two Hemispheres The surface of the brain, known as the **cerebral cortex**, is very uneven, characterized by a distinctive pattern of folds or bumps, known as **gyri** (singular: gyrus), and grooves, known as **sulci** (singular: sulcus), shown in Figure 1. These gyri and sulci form important landmarks that allow us to separate the brain into functional centers. The most prominent sulcus, known as the longitudinal fissure, is the deep groove that separates the brain into two halves or hemispheres: the left hemisphere and the right hemisphere. An illustration of the brain's exterior surface shows the ridges and depressions, and the deep fissure that runs through the center.**Figure 1. The surface of the brain is covered with gyri and sulci. A deep sulcus is called a fissure, such as the longitudinal fissure that divides the brain into left and right hemispheres. (credit: modification of work by Bruce Blaus)** There is evidence of some specialization of function---referred to as **lateralization**---in each hemisphere, mainly regarding differences in language ability. Beyond that, however, the differences that have been found have been minor (this means that it is a myth that a person is either left-brained dominant or right-brained dominant).[^[\[2\]]^](https://www.coursehero.com/study-guides/wmopen-psychology/outcome-parts-of-the-brain/#footnote-2) What we do know is that the left hemisphere controls the right half of the body, and the right hemisphere controls the left half of the body.\ \ The two hemispheres are connected by a thick band of neural fibers known as the **corpus callosum**, consisting of about 200 million axons. The corpus callosum allows the two hemispheres to communicate with each other and allows for information being processed on one side of the brain to be shared with the other side.\ \ Normally, we are not aware of the different roles that our two hemispheres play in day-to-day functions, but there are people who come to know the capabilities and functions of their two hemispheres quite well. In some cases of severe epilepsy, doctors elect to sever the corpus callosum as a means of controlling the spread of seizures (Figure 2). While this is an effective treatment option, it results in individuals who have split brains. After surgery, these split-brain patients show a variety of interesting behaviors. For instance, a split-brain patient is unable to name a picture that is shown in the patient's left visual field because the information is only available in the largely nonverbal right hemisphere. However, they are able to recreate the picture with their left hand, which is also controlled by the right hemisphere. When the more verbal left hemisphere sees the picture that the hand drew, the patient is able to name it (assuming the left hemisphere can interpret what was drawn by the left hand). Much of what we know about the functions of different areas of the brain comes from studying changes in the behavior and ability of individuals who have suffered damage to the brain. For example, researchers study the behavioral changes caused by strokes to learn about the functions of specific brain areas. A stroke, caused by an interruption of blood flow to a region in the brain, causes a loss of brain function in the affected region. The damage can be in a small area, and, if it is, this gives researchers the opportunity to link any resulting behavioral changes to a specific area. The types of deficits displayed after a stroke will be largely dependent on where in the brain the damage occurred.\ \ Consider Theona, an intelligent, self-sufficient woman, who is 62 years old. Recently, she suffered a stroke in the front portion of her right hemisphere. As a result, she has great difficulty moving her left leg. (As you learned earlier, the right hemisphere controls the left side of the body; also, the brain's main motor centers are located at the front of the head, in the frontal lobe.) Theona has also experienced behavioral changes. For example, while in the produce section of the grocery store, she sometimes eats grapes, strawberries, and apples directly from their bins before paying for them. This behavior---which would have been very embarrassing to her before the stroke---is consistent with damage in another region in the frontal lobe---the prefrontal cortex, which is associated with judgment, reasoning, and impulse control. Forebrain Structures The two hemispheres of the cerebral cortex are part of the **forebrain** (Figure 3), which is the largest part of the brain. The forebrain contains the cerebral cortex and a number of other structures that lie beneath the cortex (called subcortical structures): thalamus, hypothalamus, pituitary gland, and the limbic system (collection of structures). The cerebral cortex, which is the outer surface of the brain, is associated with higher level processes such as consciousness, thought, emotion, reasoning, language, and memory. Each cerebral hemisphere can be subdivided into four lobes, each associated with different functions. **Figure 3. The brain and its parts can be divided into three main categories: the forebrain, midbrain, and hindbrain.** Lobes of the Brain The four lobes of the brain are the frontal, parietal, temporal, and occipital lobes (Figure 4). The **frontal lobe** is located in the forward part of the brain, extending back to a fissure known as the central sulcus. The frontal lobe is involved in reasoning, motor control, emotion, and language. It contains the **motor cortex**, which is involved in planning and coordinating movement; the **prefrontal cortex**, which is responsible for higher-level cognitive functioning; and **Broca's area**, which is essential for language production. An illustration shows the four lobes of the brain.**Figure 4. The lobes of the brain are shown.** People who suffer damage to Broca's area have great difficulty producing language of any form. For example, Padma was an electrical engineer who was socially active and a caring, involved mother. About twenty years ago, she was in a car accident and suffered damage to her Broca's area. She completely lost the ability to speak and form any kind of meaningful language. There is nothing wrong with her mouth or her vocal cords, but she is unable to produce words. She can follow directions but can't respond verbally, and she can read but no longer write. She can do routine tasks like running to the market to buy milk, but she could not communicate verbally if a situation called for it. One particularly fascinating area in the frontal lobe is called the "primary motor cortex". This strip running along the side of the brain is in charge of voluntary movements like waving goodbye, wiggling your eyebrows, and kissing. It is an excellent example of the way that the various regions of the brain are highly specialized. Interestingly, each of our various body parts has a unique portion of the primary motor cortex devoted to it. Each individual finger has about as much dedicated brain space as your entire leg. Your lips, in turn, require about as much dedicated brain processing as all of your fingers and your hand combined! **Figure 7. Spatial relationships in the body are mirrored in the organization of the somatosensory cortex.** Because the cerebral cortex in general, and the frontal lobe in particular, are associated with such sophisticated functions as planning and being self-aware they are often thought of as a higher, less primal portion of the brain. Indeed, other animals such as rats and kangaroos while they do have frontal regions of their brain do not have the same level of development in the cerebral cortices. The closer an animal is to humans on the evolutionary tree---think chimpanzees and gorillas, the more developed is this portion of their brain.\ \ The brain's **parietal lobe** is located immediately behind the frontal lobe, and is involved in processing information from the body's senses. It contains the **somatosensory cortex**, which is essential for processing sensory information from across the body, such as touch, temperature, and pain. The somatosensory cortex is organized topographically, which means that spatial relationships that exist in the body are maintained on the surface of the somatosensory cortex. For example, the portion of the cortex that processes sensory information from the hand is adjacent to the portion that processes information from the wrist. An illustration shows the locations of Broca's and Wernicke's areas.**Figure 8. Damage to either Broca's area or Wernicke's area can result in language deficits. The types of deficits are very different, however, depending on which area is affected.** The **temporal lobe** is located on the side of the head (temporal means "near the temples"), and is associated with hearing, memory, emotion, and some aspects of language. The **auditory cortex**, the main area responsible for processing auditory information, is located within the temporal lobe. **Wernicke's area**, important for speech comprehension, is also located here. Whereas individuals with damage to Broca's area have difficulty producing language, those with damage to Wernicke's area can produce sensible language, but they are unable to understand it.\ \ The **occipital lobe** is located at the very back of the brain, and contains the primary visual cortex, which is responsible for interpreting incoming visual information. The occipital cortex is organized retinotopically, which means there is a close relationship between the position of an object in a person's visual field and the position of that object's representation on the cortex. You will learn much more about how visual information is processed in the occipital lobe when you study sensation and perception. Glossary **auditory cortex: **strip of cortex in the temporal lobe that is responsible for processing auditory information\ \ **Broca's area: **region in the left hemisphere that is essential for language production\ \ **cerebral cortex: **surface of the brain that is associated with our highest mental capabilities\ \ **corpus callosum: **thick band of neural fibers connecting the brain's two hemispheres\ \ **forebrain: **largest part of the brain, containing the cerebral cortex, the thalamus, and the limbic system, among other structures\ \ **frontal lobe: **part of the cerebral cortex involved in reasoning, motor control, emotion, and language; contains motor cortex\ \ **gyrus **(plural: gyri): bump or ridge on the cerebral cortex\ \ **hemisphere: **left or right half of the brain\ \ **lateralization: **concept that each hemisphere of the brain is associated with specialized functions\ \ **longitudinal fissure: **deep groove in the brain's cortex\ \ **motor cortex: **strip of cortex involved in planning and coordinating movement\ \ **occipital lobe: **part of the cerebral cortex associated with visual processing; contains the primary visual cortex\ \ **parietal lobe: **part of the cerebral cortex involved in processing various sensory and perceptual information; contains the primary somatosensory cortex\ \ **prefrontal cortex: **area in the frontal lobe responsible for higher-level cognitive functioning\ \ **somatosensory cortex: **essential for processing sensory information from across the body, such as touch, temperature, and pain\ \ **sulcus **(plural: sulci): depressions or grooves in the cerebral cortex\ \ **temporal lobe: **part of cerebral cortex associated with hearing, memory, emotion, and some aspects of language; contains primary auditory cortex\ \ **Wernicke's area: **important for speech comprehension The Limbic System and Other Brain Areas Areas of the Forebrain Other areas of the **forebrain** (which includes the lobes that you learned about previously), are the parts located beneath the cerebral cortex, including the thalamus and the limbic system. The **thalamus** is a sensory relay for the brain. All of our senses, with the exception of smell, are routed through the thalamus before being directed to other areas of the brain for processing (Figure 1). **Figure 1. The thalamus serves as the relay center of the brain where most senses are routed for processing.** The **limbic system** is involved in processing both emotion and memory. Interestingly, the sense of smell projects directly to the limbic system; therefore, not surprisingly, smell can evoke emotional responses in ways that other sensory modalities cannot. The limbic system is made up of a number of different structures, but three of the most important are the hippocampus, the amygdala, and the hypothalamus (Figure 2). The **hippocampus** is an essential structure for learning and memory. The **amygdala** is involved in our experience of emotion and in tying emotional meaning to our memories. The **hypothalamus** regulates a number of homeostatic processes, including the regulation of body temperature, appetite, and blood pressure. The hypothalamus also serves as an interface between the nervous system and the endocrine system and in the regulation of sexual motivation and behavior. An illustration shows the locations of parts of the brain involved in the limbic system: the hypothalamus, amygdala, and hippocampus.**Figure 2. The limbic system is involved in mediating emotional response and memory.** Midbrain and Hindbrain Structures The **midbrain** is comprised of structures located deep within the brain, between the forebrain and the hindbrain. The **reticular formation** is centered in the midbrain, but it actually extends up into the forebrain and down into the hindbrain. The reticular formation is important in regulating the sleep/wake cycle, arousal, alertness, and motor activity.\ \ The **substantia nigra** (Latin for "black substance") and the **ventral tegmental area (VTA)** are also located in the midbrain (Figure 3). Both regions contain cell bodies that produce the neurotransmitter dopamine, and both are critical for movement. Degeneration of the substantia nigra and VTA is involved in Parkinson's disease. In addition, these structures are involved in mood, reward, and addiction (Berridge & Robinson, 1998; Gardner, 2011; George, Le Moal, & Koob, 2012). **Figure 3. The substantia nigra and ventral tegmental area (VTA) are located in the midbrain.** The **hindbrain** is located at the back of the head and looks like an extension of the spinal cord. It contains the medulla, pons, and cerebellum (Figure 4). The **medulla** controls the automatic processes of the autonomic nervous system, such as breathing, blood pressure, and heart rate. The word **pons** literally means "bridge," and as the name suggests, the pons serves to connect the brain and spinal cord. It also is involved in regulating brain activity during sleep. The medulla, pons, and midbrain together are known as the brainstem. An illustration shows the location of the pons, medulla, and cerebellum.**Figure 4. The pons, medulla, and cerebellum make up the hindbrain.** The **cerebellum** (Latin for "little brain") receives messages from muscles, tendons, joints, and structures in our ear to control balance, coordination, movement, and motor skills. The cerebellum is also thought to be an important area for processing some types of memories. In particular, procedural memory, or memory involved in learning and remembering how to perform tasks, is thought to be associated with the cerebellum. Recall that H. M. was unable to form new explicit memories, but he could learn new tasks. This is likely due to the fact that H. M.'s cerebellum remained intact. Glossary **amygdala: **structure in the limbic system involved in our experience of emotion and tying emotional meaning to our memories **cerebellum: **hindbrain structure that controls our balance, coordination, movement, and motor skills, and it is thought to be important in processing some types of memory **cerebral cortex: **surface of the brain that is associated with our highest mental capabilities **forebrain: **largest part of the brain, containing the cerebral cortex, the thalamus, and the limbic system, among other structures **hindbrain: **division of the brain containing the medulla, pons, and cerebellum **hippocampus: **structure in the temporal lobe associated with learning and memory **hypothalamus: **forebrain structure that regulates sexual motivation and behavior and a number of homeostatic processes; serves as an interface between the nervous system and the endocrine system **limbic system: **collection of structures involved in processing emotion and memory **medulla: **hindbrain structure that controls automated processes like breathing, blood pressure, and heart rate **midbrain: **division of the brain located between the forebrain and the hindbrain; contains the reticular formation **pons: **hindbrain structure that connects the brain and spinal cord; involved in regulating brain activity during sleep **reticular formation: **midbrain structure important in regulating the sleep/wake cycle, arousal, alertness, and motor activity **thalamus: **sensory relay for the brain **ventral tegmental area (VTA): **midbrain structure where dopamine is produced: associated with mood, reward, and addiction Brain Imaging You have learned how brain injury can provide information about the functions of different parts of the brain. Increasingly, however, we are able to obtain that information using **brain imaging** techniques on individuals who have not suffered brain injury. In this section, we take a more in-depth look at some of the techniques that are available for imaging the brain, including techniques that rely on radiation, magnetic fields, or electrical activity within the brain. Techniques Involving Radiation **Figure 1. A CT scan can be used to show brain tumors. (a) The image on the left shows a healthy brain, whereas (b) the image on the right indicates a brain tumor in the left frontal lobe. (credit a: modification of work by \"Aceofhearts1968\"/Wikimedia Commons; credit b: modification of work by Roland Schmitt et al)** A **computerized tomography (CT) scan** involves taking a number of x-rays of a particular section of a person's body or brain (Figure 1). The x-rays pass through tissues of different densities at different rates, allowing a computer to construct an overall image of the area of the body being scanned. A CT scan is often used to determine whether someone has a tumor, or significant brain atrophy. A brain scan shows different parts of the brain in different colors.**Figure 2. A PET scan is helpful for showing activity in different parts of the brain. (credit: Health and Human Services Department, National Institutes of Health)** **Positron emission tomography (PET)** scans create pictures of the living, active brain (Figure 2). An individual receiving a PET scan drinks or is injected with a mildly radioactive substance, called a tracer. Once in the bloodstream, the amount of tracer in any given region of the brain can be monitored. As brain areas become more active, more blood flows to that area. A computer monitors the movement of the tracer and creates a rough map of active and inactive areas of the brain during a given behavior. PET scans show little detail, are unable to pinpoint events precisely in time, and require that the brain be exposed to radiation; therefore, this technique has been replaced by the fMRI as an alternative diagnostic tool. However, combined with CT, PET technology is still being used in certain contexts. For example, CT/PET scans allow better imaging of the activity of neurotransmitter receptors and open new avenues in schizophrenia research. In this hybrid CT/PET technology, CT contributes clear images of brain structures, while PET shows the brain's activity. **Figure 3. An fMRI shows activity in the brain over time. This image represents a single frame from an fMRI. (credit: modification of work by Kim J, Matthews NL, Park S.)** Techniques Involving Magnetic Fields In **magnetic resonance imaging (MRI)**, a person is placed inside a machine that generates a strong magnetic field. The magnetic field causes the hydrogen atoms in the body's cells to move. When the magnetic field is turned off, the hydrogen atoms emit electromagnetic signals as they return to their original positions. Tissues of different densities give off different signals, which a computer interprets and displays on a monitor. **Functional magnetic resonance imaging (fMRI)** operates on the same principles, but it shows changes in brain activity over time by tracking blood flow and oxygen levels. The fMRI provides more detailed images of the brain's structure, as well as better accuracy in time, than is possible in PET scans (Figure 3). With their high level of detail, MRI and fMRI are often used to compare the brains of healthy individuals to the brains of individuals diagnosed with psychological disorders. This comparison helps determine what structural and functional differences exist between these populations. Techniques Involving Electrical Activity In some situations, it is helpful to gain an understanding of the overall activity of a person's brain, without needing information on the actual location of the activity. **Electroencephalography (EEG)** serves this purpose by providing a measure of a brain's electrical activity. An array of electrodes is placed around a person's head (Figure 4). The signals received by the electrodes result in a printout of the electrical activity of his or her brain, or brainwaves, showing both the frequency (number of waves per second) and amplitude (height) of the recorded brainwaves, with an accuracy within milliseconds. Such information is especially helpful to researchers studying sleep patterns among individuals with sleep disorders. Glossary **computerized tomography (CT) scan: **imaging technique in which a computer coordinates and integrates multiple x-rays of a given area **electroencephalography (EEG): **recording the electrical activity of the brain via electrodes on the scalp **functional magnetic resonance imaging (fMRI): **MRI that shows changes in metabolic activity over time **magnetic resonance imaging (MRI): **magnetic fields used to produce a picture of the tissue being imaged **positron emission tomography (PET) scan: **involves injecting individuals with a mildly radioactive substance and monitoring changes in blood flow to different regions of the brain Nature and Nurture The Nature vs. Nurture Debate Are you the way you are because you were born that way, or because of the way you were raised? Do your genetics and biology dictate your personality and behavior, or is it your environment and how you were raised? These questions are central to the age-old **nature-nurture** debate. In the history of psychology, no other question has caused so much controversy and offense: We are so concerned with nature--nurture because our very sense of moral character seems to depend on it. While we may admire the athletic skills of a great basketball player, we think of his height as simply a gift, a payoff in the "genetic lottery." For the same reason, no one blames a short person for his height or someone's congenital disability on poor decisions: To state the obvious, it's "not their fault." But we do praise the concert violinist (and perhaps her parents and teachers as well) for her dedication, just as we condemn cheaters, slackers, and bullies for their bad behavior.The problem is, most human characteristics aren't usually as clear-cut as height or instrument-mastery, affirming our nature--nurture expectations strongly one way or the other. In fact, even the great violinist might have some inborn qualities---perfect pitch, or long, nimble fingers---that support and reward her hard work. And the basketball player might have eaten a diet while growing up that promoted his genetic tendency for being tall. When we think about our own qualities, they seem under our control in some respects, yet beyond our control in others. And often the traits that don't seem to have an obvious cause are the ones that concern us the most and are far more personally significant. What about how much we drink or worry? What about our honesty, or religiosity, or sexual orientation? They all come from that uncertain zone, neither fixed by nature nor totally under our own control. One major problem with answering nature-nurture questions about people is, how do you set up an experiment? In nonhuman animals, there are relatively straightforward experiments for tackling nature--nurture questions. Say, for example, you are interested in aggressiveness in dogs. You want to test for the more important determinant of aggression: being born to aggressive dogs or being raised by them. You could mate two aggressive dogs---angry Chihuahuas---together, and mate two nonaggressive dogs---happy beagles---together, then switch half the puppies from each litter between the different sets of parents to raise. You would then have puppies born to aggressive parents (the Chihuahuas) but being raised by nonaggressive parents (the Beagles), and vice versa, in litters that mirror each other in puppy distribution. The big questions are: Would the Chihuahua parents raise aggressive beagle puppies? Would the beagle parents raise *non*aggressive Chihuahua puppies? Would the puppies' *nature* win out, regardless of who raised them? Or\... would the result be a combination of nature *and* nurture? Much of the most significant nature--nurture research has been done in this way (Scott & Fuller, 1998), and animal breeders have been doing it successfully for thousands of years. In fact, it is fairly easy to breed animals for behavioral traits.\ \ With people, however, we can't assign babies to parents at random, or select parents with certain behavioral characteristics to mate, merely in the interest of science (though history does include horrific examples of such practices, in misguided attempts at "eugenics," the shaping of human characteristics through intentional breeding). In typical human families, children's biological parents raise them, so it is very difficult to know whether children act like their parents due to genetic (nature) or environmental (nurture) reasons. Nevertheless, despite our restrictions on setting up human-based experiments, we do see real-world examples of nature-nurture at work in the human sphere---though they only provide partial answers to our many questions. The science of how genes and environments work together to influence behavior is called **behavioral genetics**. The easiest opportunity we have to observe this is the **adoption study**. When children are put up for adoption, the parents who give birth to them are no longer the parents who raise them. This setup isn't quite the same as the experiments with dogs (children aren't assigned to random adoptive parents in order to suit the particular interests of a scientist) but adoption still tells us some interesting things, or at least confirms some basic expectations. For instance, if the biological child of tall parents were adopted into a family of short people, do you suppose the child's growth would be affected? What about the biological child of a Spanish-speaking family adopted at birth into an English-speaking family? What language would you expect the child to speak? And what might these outcomes tell you about the difference between height and language in terms of nature-nurture? Another option for observing nature-nurture in humans involves **twin studies**. There are two types of twins: monozygotic (MZ) and dizygotic (DZ). Monozygotic twins, also called "identical" twins, result from a single zygote (fertilized egg) and have the same DNA. They are essentially clones. Dizygotic twins, also known as "fraternal" twins, develop from two zygotes and share 50% of their DNA. Fraternal twins are ordinary siblings who happen to have been born at the same time. To analyze nature--nurture using twins, we compare the similarity of MZ and DZ pairs. Sticking with the features of height and spoken language, let's take a look at how nature and nurture apply: Identical twins, unsurprisingly, are almost perfectly similar for height. The heights of fraternal twins, however, are like any other sibling pairs: more similar to each other than to people from other families, but hardly identical. This contrast between twin types gives us a clue about the role genetics plays in determining height.\ \ Now consider spoken language. If one identical twin speaks Spanish at home, the co-twin with whom she is raised almost certainly does too. But the same would be true for a pair of fraternal twins raised together. In terms of spoken language, fraternal twins are just as similar as identical twins, so it appears that the genetic match of identical twins doesn't make much difference. Twin and adoption studies are two instances of a much broader class of methods for observing nature-nurture called **quantitative genetics**, the scientific discipline in which similarities among individuals are analyzed based on how biologically related they are. We can do these studies with siblings and half-siblings, cousins, twins who have been separated at birth and raised separately (Bouchard, Lykken, McGue, & Segal, 1990; such twins are very rare and play a smaller role than is commonly believed in the science of nature--nurture), or with entire extended families (see Plomin, DeFries, Knopik, & Neiderhiser, 2012, for a complete introduction to research methods relevant to nature--nurture).\ \ For better or for worse, contentions about nature--nurture have intensified because quantitative genetics produces a number called a **heritability coefficient**, varying from 0 to 1, that is meant to provide a single measure of genetics' influence of a trait. In a general way, a heritability coefficient measures how strongly differences among individuals are related to differences among their genes. But beware: Heritability coefficients, although simple to compute, are deceptively difficult to interpret. Nevertheless, numbers that provide simple answers to complicated questions tend to have a strong influence on the human imagination, and a great deal of time has been spent discussing whether the heritability of intelligence or personality or depression is equal to one number or another. One reason nature--nurture continues to fascinate us so much is that we live in an era of great scientific discovery in genetics, comparable to the times of Copernicus, Galileo, and Newton, with regard to astronomy and physics. Every day, it seems, new discoveries are made, new possibilities proposed. When Francis Galton first started thinking about nature--nurture in the late-19th century he was very influenced by his cousin, Charles Darwin, but genetics *per se* was unknown. Mendel's famous work with peas, conducted at about the same time, went undiscovered for 20 years; quantitative genetics was developed in the 1920s; DNA was discovered by Watson and Crick in the 1950s; the human genome was completely sequenced at the turn of the 21st century; and we are now on the verge of being able to obtain the specific DNA sequence of anyone at a relatively low cost. No one knows what this new genetic knowledge will mean for the study of nature--nurture, but as we will see in the next section, answers to nature--nurture questions have turned out to be far more difficult and mysterious than anyone imagined. What Have We Learned About Nature--Nurture? It would be satisfying to be able to say that nature--nurture studies have given us conclusive and complete evidence about where traits come from, with some traits clearly resulting from genetics and others almost entirely from environmental factors, such as childrearing practices and personal will; but that is not the case. Instead, *everything* has turned out to have some footing in genetics. The more genetically-related people are, the more similar they are---for *everything*: height, weight, intelligence, personality, mental illness, etc. Sure, it seems like common sense that some traits have a genetic bias. For example, adopted children resemble their biological parents even if they have never met them, and identical twins are more similar to each other than are fraternal twins. And while certain psychological traits, such as personality or mental illness (e.g., schizophrenia), seem reasonably influenced by genetics, it turns out that the same is true for political attitudes, how much television people watch (Plomin, Corley, DeFries, & Fulker, 1990), and whether or not they get divorced (McGue & Lykken, 1992). Mother splashing with daughter in a fountain.**Figure 4. Research over the last half century has revealed how central genetics are to behavior. The more genetically related people are the more similar they are not just physically but also in terms of personality and behavior. \[Photo: 藍川芥 aikawake\]** It may seem surprising, but genetic influence on behavior is a relatively recent discovery. In the middle of the 20th century, psychology was dominated by the doctrine of behaviorism, which held that behavior could only be explained in terms of environmental factors. Psychiatry concentrated on psychoanalysis, which probed for roots of behavior in individuals' early life-histories. The truth is, neither behaviorism nor psychoanalysis is incompatible with genetic influences on behavior, and neither Freud nor Skinner was naive about the importance of organic processes in behavior. Nevertheless, in their day it was widely thought that children's personalities were shaped entirely by imitating their parents' behavior, and that schizophrenia was caused by certain kinds of "pathological mothering."\ \ Whatever the outcome of our broader discussion of nature--nurture, the basic fact that the best predictors of an adopted child's personality or mental health are found in the biological parents he or she has never met, rather than in the adoptive parents who raised him or her, presents a significant challenge to purely environmental explanations of personality or psychopathology. The message is clear: You can't leave genes out of the equation. But keep in mind, no behavioral traits are completely inherited, so you can't leave the environment out altogether, either. Trying to untangle the various ways nature-nurture influences human behavior can be messy, and often common-sense notions can get in the way of good science. One very significant contribution of behavioral genetics that has changed psychology for good can be very helpful to keep in mind: When your subjects are biologically-related, no matter how clearly a situation may seem to point to environmental influence, it is never safe to interpret a behavior as wholly the result of nurture without further evidence. For example, when presented with data showing that children whose mothers read to them often are likely to have better reading scores in third grade, it is tempting to conclude that reading to your kids out loud is important to success in school; this may well be true, but the study as described is inconclusive, because there are genetic *as well as *environmental pathways between the parenting practices of mothers and the abilities of their children. This is a case where "correlation does not imply causation," as they say. To establish that reading aloud causes success, a scientist can either study the problem in adoptive families (in which the genetic pathway is absent) or by finding a way to randomly assign children to oral reading conditions. Psychological researchers study genetics in order to better understand the biological basis that contributes to certain behaviors. While all humans share certain biological mechanisms, we are each unique. And while our bodies have many of the same parts---brains and hormones and cells with genetic codes---these are expressed in a wide variety of behaviors, thoughts, and reactions.\ \ Why do two people infected by the same disease have different outcomes: one surviving and one succumbing to the ailment? How are genetic diseases passed through family lines? Are there genetic components to psychological disorders, such as depression or schizophrenia? To what extent might there be a psychological basis to health conditions such as childhood obesity?\ \ To explore these questions, let's start by focusing on a specific disease, sickle-cell anemia, and how it might affect two infected sisters. **Sickle-cell anemia** is a genetic condition in which red blood cells, which are normally round, take on a crescent-like shape (Figure 5). The changed shape of these cells affects how they function: sickle-shaped cells can clog blood vessels and block blood flow, leading to high fever, severe pain, swelling, and tissue damage. **Figure 5. Normal blood cells travel freely through the blood vessels, while sickle-shaped cells form blockages preventing blood flow.** Many people with sickle-cell anemia---and the particular genetic mutation that causes it---die at an early age. While the notion of "survival of the fittest" may suggest that people suffering from this disease have a low survival rate and therefore the disease will become less common, this is not the case. Despite the negative evolutionary effects associated with this genetic mutation, the sickle-cell gene remains relatively common among people of African descent. Why is this? The explanation is illustrated with the following scenario.\ \ Imagine two young women---Luwi and Sena---sisters in rural Zambia, Africa. Luwi carries the gene for sickle-cell anemia; Sena does not carry the gene. Sickle-cell carriers have one copy of the sickle-cell gene but do not have full-blown sickle-cell anemia. They experience symptoms only if they are severely dehydrated or are deprived of oxygen (as in mountain climbing). Carriers are thought to be immune from malaria (an often deadly disease that is widespread in tropical climates) because changes in their blood chemistry and immune functioning prevent the malaria parasite from having its effects (Gong, Parikh, Rosenthal, & Greenhouse, 2013). However, full-blown sickle-cell anemia, with two copies of the sickle-cell gene, does not provide immunity to malaria.\ \ While walking home from school, both sisters are bitten by mosquitos carrying the malaria parasite. Luwi does not get malaria because she carries the sickle-cell mutation. Sena, on the other hand, develops malaria and dies just two weeks later. Luwi survives and eventually has children, to whom she may pass on the sickle-cell mutation. Malaria is rare in the United States, so the sickle-cell gene benefits nobody: the gene manifests primarily in health problems---minor in carriers, severe in the full-blown disease---with no health benefits for carriers. However, the situation is quite different in other parts of the world. In parts of Africa where malaria is prevalent, having the sickle-cell mutation does provide health benefits for carriers (protection from malaria).\ \ This is precisely the situation that Charles Darwin describes in the **theory of evolution by natural selection** (Figure 6). In simple terms, the theory states that organisms that are better suited for their environment will survive and reproduce, while those that are poorly suited for their environment will die off. In our example, we can see that as a carrier, Luwi's mutation is highly adaptive in her African homeland; however, if she resided in the United States (where malaria is much less common), her mutation could prove costly---with a high probability of the disease in her descendants and minor health problems of her own. Genetic Variation Genetic variation, the genetic difference between individuals, is what contributes to a species' adaptation to its environment. In humans, genetic variation begins with an egg, about 100 million sperm, and fertilization. Fertile women ovulate roughly once per month, releasing an egg from follicles in the ovary. The egg travels, via the fallopian tube, from the ovary to the uterus, where it may be fertilized by a sperm.\ \ The egg and the sperm each contain 23 chromosomes. **Chromosomes** are long strings of genetic material known as **deoxyribonucleic acid (DNA)**. DNA is a helix-shaped molecule made up of nucleotide base pairs. In each chromosome, sequences of DNA make up **genes** that control or partially control a number of visible characteristics, known as traits, such as eye color, hair color, and so on. A single gene may have multiple possible variations, or alleles. An **allele** is a specific version of a gene. So, a given gene may code for the trait of hair color, and the different alleles of that gene affect which hair color an individual has.\ \ When a sperm and egg fuse, their 23 chromosomes pair up and create a zygote with 23 pairs of chromosomes. Therefore, each parent contributes half the genetic information carried by the offspring; the resulting physical characteristics of the offspring (called the phenotype) are determined by the interaction of genetic material supplied by the parents (called the genotype). A person's **genotype** is the genetic makeup of that individual. **Phenotype,** on the other hand, refers to the individual's inherited physical characteristics (Figure 7). Most traits are controlled by multiple genes, but some traits are controlled by one gene. A characteristic like **cleft chin**, for example, is influenced by a single gene from each parent. In this example, we will call the gene for cleft chin "B," and the gene for smooth chin "b." Cleft chin is a dominant trait, which means that having the **dominant allele** either from one parent (Bb) or both parents (BB) will always result in the phenotype associated with the dominant allele. When someone has two copies of the same allele, they are said to be **homozygous** for that allele. When someone has a combination of alleles for a given gene, they are said to be **heterozygous**. For example, smooth chin is a recessive trait, which means that an individual will only display the smooth chin phenotype if they are homozygous for that **recessive allele** (bb).\ \ Imagine that a woman with a cleft chin has a child with a man with a smooth chin. What type of chin will their child have? The answer to that depends on which alleles each parent carries. If the woman is homozygous for cleft chin (BB), her offspring will always have cleft chin. It gets a little more complicated, however, if the mother is heterozygous for this gene (Bb). Since the father has a smooth chin---therefore homozygous for the recessive allele (bb)---we can expect the offspring to have a 50% chance of having a cleft chin and a 50% chance of having a smooth chin Sickle-cell anemia is just one of many genetic disorders caused by the pairing of two recessive genes. For example, **phenylketonuria (PKU)** is a condition in which individuals lack an enzyme that normally converts harmful amino acids into harmless byproducts. If someone with this condition goes untreated, he or she will experience significant deficits in cognitive function, seizures, and increased risk of various psychiatric disorders. Because PKU is a recessive trait, each parent must have at least one copy of the recessive allele in order to produce a child with the condition (Figure 9). So far, we have discussed traits that involve just one gene, but few human characteristics are controlled by a single gene. Most traits are **polygenic**: controlled by more than one gene. Height is one example of a polygenic trait, as are skin color and weight. Where do harmful genes that contribute to diseases like PKU come from? Gene mutations provide one source of harmful genes. A **mutation** is a sudden, permanent change in a gene. While many mutations can be harmful or lethal, once in a while, a mutation benefits an individual by giving that person an advantage over those who do not have the mutation. Recall that the theory of evolution asserts that individuals best adapted to their particular environments are more likely to reproduce and pass on their genes to future generations. In order for this process to occur, there must be competition---more technically, there must be variability in genes (and resultant traits) that allow for variation in adaptability to the environment. If a population consisted of identical individuals, then any dramatic changes in the environment would affect everyone in the same way, and there would be no variation in selection. In contrast, diversity in genes and associated traits allows some individuals to perform slightly better than others when faced with environmental change. This creates a distinct advantage for individuals best suited for their environments in terms of successful reproduction and genetic transmission. Glossary **adoption study**: a behavior genetic research method that involves comparison of adopted children to their adoptive and biological parents **allele: **specific version of a gene **behavioral genetics**: the empirical science of how genes and environments combine to generate behavior **chromosome: **long strand of genetic information **deoxyribonucleic acid (DNA): **helix-shaped molecule made of nucleotide base pairs **dominant allele: **allele whose phenotype will be expressed in an individual that possesses that allele **genetic environmental correlation: **view of gene-environment interaction that asserts our genes affect our environment, and our environment influences the expression of our genes **genotype: **genetic makeup of an individual **heterozygous: **consisting of two different alleles **heritability coefficient**: an easily misinterpreted statistical construct that purports to measure the role of genetics in the explanation of differences among individuals **homozygous: **consisting of two identical alleles **mutation: **sudden, permanent change in a gene **phenotype: **individual's inheritable physical characteristics **polygenic: **multiple genes affecting a given trait **quantitative genetics**: scientific and mathematical methods for inferring genetic and environmental processes based on the degree of genetic and environmental similarity among organisms **recessive allele: **allele whose phenotype will be expressed only if an individual is homozygous for that allele **theory of evolution by natural selection: **states that organisms that are better suited for their environments will survive and reproduce compared to those that are poorly suited for their environments **twin studies**: a behavior genetic research method that involves comparison of the similarity of identical (monozygotic; MZ) and fraternal (dizygotic; DZ) twins Gene-Environment Interactions Genes do not exist in a vacuum. Although we are all biological organisms, we also exist in an environment that is incredibly important in determining not only when and how our genes express themselves, but also in what combination. Each of us represents a unique interaction between our genetic makeup and our environment; range of reaction is one way to describe this interaction. **Range of reaction** asserts that our genes set the boundaries within which we can operate, and our environment interacts with the genes to determine where in that range we will fall. For example, if an individual's genetic makeup predisposes her to high levels of intellectual potential and she is reared in a rich, stimulating environment, then she will be more likely to achieve her full potential than if she were raised under conditions of significant deprivation. According to the concept of range of reaction, genes set definite limits on potential, and environment determines how much of that potential is achieved.\ \ Another perspective on the interaction between genes and the environment is the concept of **genetic environmental correlation**. Stated simply, our genes influence our environment, and our environment influences the expression of our genes (Figure 1). Not only do our genes and environment interact, as in range of reaction, but they also influence one another bidirectionally. For example, the child of an NBA player would probably be exposed to basketball from an early age. Such exposure might allow the child to realize his or her full genetic, athletic potential. Thus, the parents' genes, which the child shares, influence the child's environment, and that environment, in turn, is well suited to support the child's genetic potential. In another approach to gene-environment interactions, the field of **epigenetics** looks beyond the genotype itself and studies how the same genotype can be expressed in different ways. In other words, researchers study how the same genotype can lead to very different phenotypes. As mentioned earlier, gene expression is often influenced by environmental context in ways that are not entirely obvious. For instance, identical twins share the same genetic information (**identical twins** develop from a single fertilized egg that split, so the genetic material is exactly the same in each; in contrast, **fraternal twins** develop from two different eggs fertilized by different sperm, so the genetic material varies as with non-twin siblings). But even with identical genes, there remains an incredible amount of variability in how gene expression can unfold over the course of each twin's life. Sometimes, one twin will develop a disease and the other will not. In one example, Tiffany, an identical twin, died from cancer at age 7, but her twin, now 19 years old, has never had cancer. Although these individuals share an identical genotype, their phenotypes differ as a result of how that genetic information is expressed over time. The epigenetic perspective is very different from range of reaction, because here the genotype is not fixed and limited. **Genes** affect more than our physical characteristics. Indeed, scientists have found genetic linkages to a number of behavioral characteristics, ranging from basic personality traits to sexual orientation to spirituality (for examples, see Mustanski et al., 2005; Comings, Gonzales, Saucier, Johnson, & MacMurray, 2000). Genes are also associated with temperament and a number of psychological disorders, such as depression and schizophrenia. So while it is true that genes provide the biological blueprints for our cells, tissues, organs, and body, they also have significant impact on our experiences and our behaviors.\ \ Let's look at the following findings regarding schizophrenia in light of our three views of gene-environment interactions. Which view do you think best explains this evidence?\ \ In a study of people who were given up for adoption, adoptees whose biological mothers had schizophrenia *and* who had been raised in a disturbed family environment were much more likely to develop schizophrenia or another psychotic disorder than were any of the other groups in the study: - - - - The study shows that adoptees with high genetic risk were especially likely to develop schizophrenia only if they were raised in disturbed home environments. This research lends credibility to the notion that both genetic vulnerability and environmental stress are necessary for schizophrenia to develop, and that genes alone do not tell the full tale. Glossary **epigenome:** a dynamic layer of information associated with DNA that differs between individuals and can be altered through various experiences and environments **epigenetics: **study of gene-environment interactions, such as how the same genotype leads to different phenotypes **fraternal twins: **twins who develop from two different eggs fertilized by different sperm, so their genetic material varies the same as in non-twin siblings **gene: **sequence of DNA that controls or partially controls physical characteristics **identical twins: **twins that develop from the same sperm and egg **range of reaction: **asserts our genes set the boundaries within which we can operate, and our environment interacts with the genes to determine where in that range we will fall