Nyki's Ch. 11 PPT S19.ppt

Chapter 11 Functional Organization of Nervous Tissue 11-1 Overview of the Nervous System • The nervous system, along with the endocrine system, helps to keep controlled conditions within limits that maintain health and helps to maintain homeostasis. • The nervous system is responsible for all ou...

Chapter 11 Functional Organization of Nervous Tissue 11-1 Overview of the Nervous System • The nervous system, along with the endocrine system, helps to keep controlled conditions within limits that maintain health and helps to maintain homeostasis. • The nervous system is responsible for all our behaviors, memories, and movements. • The branch of medical science that deals with the normal functioning and disorders of the nervous system is called neurology. Copyright 2009 John Wiley & Sons, Inc. 11-2 Major Structures of the Nervous System Copyright 2009 John Wiley & Sons, Inc. Diff Text. Fig 11.0; Slide# 11-3 Functions of the Nervous System • Sensory function: to sense changes in the internal and external environment through sensory receptors. – Sensory (afferent) neurons serve this function. • Integrative function: to analyze the sensory information, store some aspects, and make decisions regarding appropriate behaviors. – Association or interneurons serve this function. • Motor function: to respond to stimuli by initiating action. – Motor(efferent) neurons serve this function. Copyright 2009 John Wiley & Sons, Inc. 11-4 11.2 Divisions of the Nervous System 1. Central nervous system (CNS): brain and spinal cord 2. Peripheral nervous system (PNS): sensory receptors and nerves • Nervous System Includes: – Brain, spinal cord, Cranial nerves & related branches, Spinal nerves & related branches, ganglia, enteric plexus, & sensory receptors 11-5 Overview of Major Structures • Nervous system structures – Brain and 12 pairs of cranial nerves and their branches – Spinal cord and thirty-one pairs of spinal nerves which emerge from the spinal cord. – Ganglia located outside the brain and spinal cord • Small masses of nervous tissue, containing primarily cell bodies of neurons. – Enteric plexuses which help regulate the digestive system. – Sensory receptors • Parts of neurons or specialized cells that monitor changes in the internal or external environment. Copyright 2009 John Wiley & Sons, Inc. 11-6 PNS • Sensory receptors: ending of neurons or separate, specialized cells that detect such things as temperature, pain, touch, pressure, light, sound, odors • Nerve: a bundle of axons and their sheaths that connects CNS to sensory receptors, muscles, and glands – Cranial nerves: originate from the brain; 12 pairs – Spinal nerves: originate from spinal cord; 31 pairs • Ganglion: collection of neuron cell bodies outside CNS • Plexus: extensive network of axons, and sometimes neuron cell bodies, located outside CNS 11-7 Divisions of PNS Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Dorsal root of spinal nerve Dorsal root ganglion Sensory neuron • Sensory (afferent): transmits action potentials from receptors to CNS. • Motor (efferent): transmits action potentials from CNS to effectors (muscles, glands) Spinal cord Spinal nerve Sensory receptor (a) Sensory division Motor neuron Spinal cord Skeletal muscle Ventral root of spinal nerve Spinal nerve (b) Somatic nervous system Fig. 11.3 (a) & (b); Slide# 11-8 Motor Division of PNS • Somatic nervous system: from CNS to skeletal muscles. – Voluntary. – Single neuron system. – Synapse: junction of a nerve cell with another cell. E.g., neuromuscular junction is a synapse between a neuron and skeletal muscle cell. • Autonomic nervous system (ANS): from CNS to smooth muscle, cardiac muscle and certain glands. – Subconscious or involuntary control. – Two neuron system: first from CNS to ganglion; second from ganglion to effector. – Divisions of ANS • Sympathetic. Prepares body for physical activity. • Parasympathetic. Regulates resting or vegetative functions such as digesting food or emptying of the urinary bladder. • Enteric. plexuses within the wall of the digestive tract. Can control the digestive tract independently of the CNS, but still considered part of ANS because of the parasympathetic and sympathetic neurons that contribute to the plexi. 11-9 Autonomic Nervous System Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Spinal nerve Autonomic ganglion Spinal cord First motor neuron Second motor neuron Effector organ (e.g., smooth muscle) Large intestine (c) Autonomic nervous system Fig. 11.3 (c); Slide# 11-10 Organization of the Nervous System Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Sensory input Motor output Effectors: cardiac and smooth muscle; glands Sympathetic division Parasympathetic division Autonomic nervous system Sensory division Effectors: Skeletal muscle Somatic nervous system Motor division PNS Receptors, nerves, ganglia, plexuses Sensory Motor CNS Brain, spinal cord (left): © Brand X Pictures/PunchStock RF; (right): © Royalty-Free/Corbis RF Receptor  Sensory NS  CNS  Motor NS  Effector Fig. 11.2; Slide# 11-11 11.3 Cells of Nervous System • Neuroglia – Support and protect neurons • Neurons or nerve cells receive stimuli and transmit action potentials – Organization • Cell body or soma • Dendrites: input • Axons: output 11-12 Parts of the Neuron Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. • Neuron Cell Body. Nucleus, Nissl substance. – Nissl substance = chromatophilic substance = rough E.R: primary site of protein synthesis. • Dendrites: short, often highly branched. – Dendritic spines: little protuberance where axons synapse with dendrite. • Axons. Can branch to form collaterals. – Axon hillock – Initial segment: beginning of axon – Trigger zone: site where action potentials are generated; axon hillock and part of axon nearest cell body – Axoplasm – Axolemma – Presynaptic terminals (terminal boutons) – Synaptic vesicles Dendrites Dendritic spine Mitochondrion Golgi apparatus Nucleolus Nucleus Neuron cell body Nissl bodies Trigger zone Axon hillock Initial segment Axon Myelin sheath formed by Schwann cell Schwann cell Collateral axon Node of Ranvier Presynaptic terminals Fig. 11.4; Slide# 11-13 Axonic Transport Mechanisms • Axoplasm moved from cell body toward terminals. Supply for growth, repair, renewal. Can move cytoskeletal proteins, organelles away from cell body toward axon terminals. • Into cell body: damaged organelles, recycled plasma membrane, and substances taken in by endocytosis can be transported up axon to cell body. Rabies and herpes virus can enter axons in damaged skin and be transported to CNS. 11-14 Types of Neurons • Functional classification – Sensory or afferent: action potentials toward CNS – Motor or efferent: action potentials away from CNS – Interneurons or association neurons: within CNS from one neuron to another • Structural classification – Multipolar: most neurons in CNS; motor neurons – Bipolar: sensory in retina of the eye and nose – Unipolar: single process that divides into two branches. Part that extends to the periphery has dendrite-like sensory receptors Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Sensory receptors Dendrites Dendrite Cell body Cell body Cell body Axon Axon Axon Axon branches function as a single axon. Fig. 11.5; Slide# 11-15 (a) A multipolar neuron has (b) A bipolar neuron has a many dendrites and an axon. dendrite and an axon. (c) A pseudo-unipolar neuron appears to have an axon and no dendrites. Structural Classification of Neurons Copyright 2009 John Wiley & Sons, Inc. Diff Text 11.1; Slide# 11-16 Neuroglia of the CNS: Astrocytes Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Neuron Foot processes Astrocyte Capillary • Processes form feet that cover the surfaces of neurons and blood vessels and the pia mater. • Regulate what substances reach the CNS from the blood (blood-brain barrier). Lots of microfilaments for support. • Produce chemicals that promote tight junctions to form blood-brain barrier – Blood-brain barrier: protects neurons from toxic substances, allows the exchange of nutrients and waste products between neurons and blood, prevents fluctuations in the composition of the blood from affecting the functions of the brain. • Regulate extracellular brain fluid composition From Table 11.1; Slide# 11-17 Neuroglia of the CNS: Ependymal Cells • Line brain ventricles and spinal cord central canal. Cilia Specialized versions of ependymal form choroid plexuses. • Choroid plexus within Ependymal certain regions of ventricles. cells Secrete cerebrospinal fluid. Cilia help move fluid thru the cavities of the brain. Have Ependymal cells long processes on basal surface that extend within the brain tissue, may have astrocyte-like functions. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. (a) (b) From Table 11.1; Slide# 11-18 Neuroglia of the CNS: Microglia and Oligodendrocytes • Microglia: specialized macrophages. Respond to inflammation, phagocytize necrotic tissue, microorganisms, and foreign substances that invade the CNS. • Oligodendrocytes: form myelin sheaths if surrounding axon. Single oligodendrocytes can form myelin sheaths around portions of several axons. Microglial cell Oligodendrocyte Nodeof Ranvier Axon Myelin sheath Part of another oligodendrocyte From Table 11.1; Slide# 11-19 Neuroglia of the CNS Diff Text 11. 2 (a); Slide# 11-20 Neuroglia of the PNS • Schwann cells or neurolemmocytes: wrap around portion of only one axon to form myelin sheath. Wrap around many times. During development, as cells grow around axon, cytoplasm is squeezed out and multiple layers of cell membrane wrap the axon. Cell membrane primarily phospholipid. • Satellite cells: surround neuron cell bodies in sensory ganglia, provide support and nutrients 11-21 Neuroglia of the PNS Diff Text 11. 2 (b); Slide# 11-22 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. TABLE 11.1 Types of Neuroglial Cells Neuroglial Cells Function CNS Astrocytes Neuron Foot processes Neuroglial Cells Function Microglia Microglia are phagocytic cells within the CNS. Astrocyte foot Processes cover the surfaces of neurons, blood vessels, and the pia mater membrane of the brain and spinal cord.The astrocytes provide structural support and play a role in regulating what substances from the blood reach the neurons. Microglial cell Oligodendrocytes Astrocyte Capillary Oligodendrocyte Ependymal cells Cilia (a) Ependymal cells (a) Ciliatedependymal cells lining the ventricles of the brain and the central canal of the spinal cord help move cerebro spinal fluid. (b) Ependymal cells on the surface of the choroid plexus secrete cerebro spinal fluid. Nodeof Ranvier Axon Myelin sheath Part of another oligodendrocyte PNS Neuron cell bodies within ganglia are surrounded by satellite cells.Schwann cells form the myelin sheath of an axon within the PNS. Schwann cells and satellite cells Ependymal cells Extensions from oligodendrocytes form part of the myelin sheaths of several axons within the CNS. Satellite cells Neuron cellbody (b) Schwann cells Node of Ranvier Axon Myelinsheath Table 11.1; Slide# 11-23 Myelinated and Unmyelinated Axons • Myelinated axons – Myelin protects and insulates axons from one another, speeds transmission, functions in repair of axons. – Not continuous – Nodes of Ranvier – Completion of development of myelin sheaths at 1 yr. – Degeneration of myelin sheaths occurs in multiple sclerosis and some cases of diabetes mellitus. • Unmyelinated axons: rest in invaginations of Schwann cells or oligodendrocytes. Not wrapped around the axon; gray matter. 11-24 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Node of Ranvier (no myelin sheath) Sc hw an nc ell Nucleus 1 Cytoplasm Sc hw a Axon nn c ell 2 Myelin sheath (a) Myelinated axon Sc hw an n Nucleus ce ll 1 Cytoplasm Sc hw an n (b) Unmyelinated axons ce ll Axons 2 Fig. 11.6; Slide# 11-25 11.4 Organization of Nervous Tissue • Gray matter: unmyelinated axons, cell bodies, dendrites, neuroglia. Integrative functions • White matter: myelinated axons. Nerve tracts propagate action potentials from one area in the CNS to another • In brain: gray is outer cortex as well as inner nuclei; white is deeper. • In spinal cord: white is outer, gray is deeper. • PNS gray matter is groups of cell bodies called ganglia 11-26 11.5 Electrical Signals • Neurons produce electrical signals called action potentials • Transfer of information from one part of body to another • Electrical properties result from ionic concentration differences across plasma membrane and permeability of membrane 11-27 Concentration Differences Across the Plasma Membrane • These ion concentrations are a result of two processes: the Na/K pump and membrane permeability. Note high concentration of Na and Cl ions outside and high concentration of K and proteins on inside. Note steep concentration gradient of Na and K, but in opposite directions. Table 11.2; Slide# 11-28 Permeability Characteristics of the Plasma Membrane • Proteins: synthesized inside cell: Large, don't dissolve in phospholipids of membrane. Proteins are negatively charged. • Cl- are repelled by proteins and they exit thru always-open nongated Cl- channels. • Gated ion channels open and close because of some sort of stimulus. When they open, they change the permeability of the cell membrane. – Ligand-gated: molecule that binds to a receptor; protein or glycoprotein 11-29 Leak Channels • Many more of these for K+ and Cl- than for Na+. So, at rest, more K+ and Cl- are moving than Na+. How are they moving? Protein repels Cl-, they move out. K+ are in higher concentration on inside than out, they move out. – Always open and responsible for permeability when membrane is at rest. – Specific for one type of ion although not absolute. 11-30 Leak Channels Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Pr¯ Pr¯ 2 There are more K+ leak channels than Na+ leak channels. In the resting cell, only the leak channels are opened; the gated channels (not shown) are closed. Because of the ion concentration differences across the membrane, K+ diffuses out of the cell down its concentration gradient and Na + diffuses into the cell down its concentration gradient. The tendency for K+ to diffuse out of the cell is opposed by the tendency of the positively charged K+ to be attracted back into the cell by the negatively charged proteins. Fig. 11.7; Slide# 11-31 Ligand Gated Ion Channels • Gated ion channels. Gated ion channels open and close because of some sort of stimulus. When they open, they change the permeability of the cell membrane. – Ligand-gated: open or close in response to ligand such as ACh binding to receptor protein. Receptor proteins are usually glycoproteins. E.g., acetylcholine binds to acetylcholine receptor on a Na+ channel. Channel opens, Na+ enters the cell. 11-32 Voltage Gated Ion Channels • Voltage-gated: open or close in response to small voltage changes across the cell membrane. • At rest, membrane is negative on the inside relative to the outside. • When cell is stimulated, that relative charge changes and voltage-gated ion channels either open or close. Most common voltage gated are Na+ and K+. In cardiac and smooth muscle, Ca2+ are important. 11-33 Other Gated Ion Channels • Touch receptors: respond to mechanical stimulation of the skin • Temperature receptors: respond to temperature changes in the skin 11-34 Establishing the Resting Membrane Potential Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Oscilloscope + + + + + – – – – + + + + – – – – – – – – – – + + + + + – – – – 0 mV –70 + + + + Neuron (b) Time • Number of charged molecules and ions inside and outside cell nearly equal • Concentration of K+ higher inside than outside cell, Na+ higher outside than inside • Potential difference: unequal distribution of charge exists between the immediate inside and immediate outside of the plasma membrane: -70 to -90 mV • The resting membrane potential Fig . 11.7; Slide# 11-35 Establishing the Resting Potential • At equilibrium there is very little movement of K+ or other ions across plasma membrane (Movement of K out through leakage channels = movement of ions is due to attraction to trapped proteins: N.B. leakage channels work in both directions. Movement of ions depends upon concentration gradient.) • Na+, Cl-, and Ca2+ do not have a great affect on resting potential since there are very few leakage channels for these ions. • If leakage channels alone were responsible for resting membrane potential, in time Na+ and K+ ion concentrations would eventually equalize. • But they are maintained by the Na/K pump. For each ATP that is consumed, three Na moved out, two K+ moved in. Outside of plasma membrane slightly positive 11-36 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Na+ K+ K leak channel Pr¯ Na+ leak channel Pr¯ Pr¯ 1 In a resting cell, there is a higher concentration of K+ (purple circles) inside the cell membrane and a higher concentration of Na+ (pink circles) outside the cell membrane. Because the membrane is not permeable to negatively charged proteins (green) they are isolated to inside of the cell membrane. Pr¯ Pr¯ 2 There are more K+ leak channels than Na+ leak channels. In the resting cell, only the leak channels are opened; the gated channels (not shown) are closed. Because of the ion concentration differences across the membrane, K+ diffuses out of the cell down its concentration gradient and Na+ diffuses into the cell down its concentration gradient. The tendency for K+ to diffuse out of the cell is opposed by the tendency of the positively charged K+ to be attracted back into the cell by the negatively charged proteins. Sodiumpotassium pump Pr¯ ATP ADP 3 The sodium-potassium pump helps maintain the differential levels of Na+ and K+ by pumping three Na+ out of the cell in exchange for two K+ into the cell. The pump is driven by ATP hydrolysis. The resting membrane potential is established when the movement of K+ out of the cell is equal to the movement of K+ into the cell. (a) Fig.11.7 (a); Slide# 11-37 Table 11.3; Slide# 11-38 Changing the Resting Membrane Potential: K+ • Depolarization: Potential difference becomes smaller or less polar • Hyperpolarization: Potential difference becomes greater or more polar • K+ concentration gradient alterations – If extracellular concentration of K+ increases: less gradient between inside and outside. Depolarization – If extracellular ion concentration decreases: steeper gradient between inside and outside. Hyperpolarization • K+ membrane permeability changes. In resting membrane, K+ in and out is equal through the leakage channels. But there are also gated K+ channels in the membrane. If they open, more K+ diffuses out but this is opposed by the negative charge that starts to develop as the K+ diffuses out. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. (mV) 0 70 Depolarization: movement of RMP toward zero Time (a) 0 (mV) Hyperpolarization: movement of RMP further away from zero 70 Time (b) Fig. 11.8(a & b); slide# 11-39 Changes in Resting Membrane Potential: Na+ • Na+ membrane permeability. • Change the concentration of Na+ inside or outside the cell, little effect because gates remain closed. • But open gates (like when ACh attaches to receptors), Na+ diffuses in, depolarizing the membrane. 11-40 Changes in Resting Membrane Potential: Ca2+ • Voltage-gated Na+ channels sensitive to changes in extracellular Ca2+ concentrations – If extracellular Ca2+ concentration decreasesNa+ gates open and membrane depolarizes. – If extracellular concentration of Ca2+ increasesgates close and membrane repolarizes or becomes hyperpolarized. 11-41 Overview of Nervous System Functions Diff Text 11.3; Slide# 11-42 Graded Potentials (mv) 0 –70 1 2 3 4 Successively stronger stimuli of short duration from 1–4 Time (a) 0 (mv) • Result from – Ligands binding to receptors – Changes in charge across membrane – Mechanical stimulation – Temperature changes – Spontaneous change in permeability • Graded – Magnitude varies from small to large depending on stimulus strength or frequency • Can summate or add onto each other • Spread (are conducted) over the plasma membrane in a decremental fashion: rapidly decrease in magnitude as they spread over the surface of the plasma membrane. • Can cause generation of action potentials –70 1 2 Two equal stimuli in short succession at 1 and 2 Time (b) Fig 11.9; Slide# 11-43 Table 11.4; Slide# 11-44 Action Potentials • Depolarization phase followed by repolarization phase. Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. – Depolarization: more positive – Repolarization: more negative (may get afterpotential [slight hyperpolarization]) +35 0 Depolarization Repolarization (mV) • Series of permeability changes when a graded potential causes depolarization of membrane. A large enough graded potential may cause the membrane to reach threshold. Then get action potential. • All-or-none principle. No matter how strong the stimulus, as long as it is greater than threshold, then action potential will occur. Threshold –70 Graded potential Afterpotential Time (ms) Fig 11.11; Slide# 11-45 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 1 Action potential propagation Trigger zone 3 2 1 Action potentials in the communicating neuron stimulate graded potentials in a receiving neuron that can summate at the trigger zone. 2 Action potentials are propagated down the axon to the axon terminal. 3 Action potentials result in communication of the neuron with its target. Fig 11.10; Slide# 11-46 Action Potentials Copyright 2009 John Wiley & Sons, Inc. Diff Text 11.4; Slide# 11-47 Stimulus Strength and Action Potential Generation Copyright 2009 John Wiley & Sons, Inc. Diff Text 11.5; Slide# 11-48 Copyright 2009 John Wiley & Sons, Inc. Diff Text 11.6; Slide# 11-49 Table 11.5; Slide# 11-50 Operation of Gates: Action Potential Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Voltage-gated Na+ channel Voltage-gated K+ channel Extracellular fluid Resting membrane potential. Na+ channels (pink) and most, but not all, K+ channels (purple) are closed. The outside of the plasma membrane is positively charged compared to the inside. Open inactivation gate Open activation gate 2 0 Threshold –70 +35 Na+ Na+ channels open. Na+ Depolarization. Na+ channels open. K+ channels begin to open. Depolarization results because the inward movement of Na+ makes the inside of the membrane more positive. Closed activation gate 2 Local potential Threshold –70 +35 Membrane potential (mV) K+ diffuse out of cell. K+ channels open. K+ Na+ channels close. Resting membrane potential Repolarization 0 3 Resting membrane potential Threshold –70 Time (ms) K+ +35 Membrane potential (mV) Na+ channel Activation gate closed Depolarization 0 Time (ms) Repolarization. Na+ channels close and additional K+ channels open. Na+ movement into the cell stops, and K+ movement out of the cell increases, causing repolarization. Closed inactivation gate 4 Resting membrane potential K+ Na+ diffuse into cell. 3 1 T ime (ms) Cytoplasm Membrane potential (mV) 1 +35 Membrane potential (mV) Closed activation gate Na+ End of repolarization and afterpotential. Voltage-gated Na+ channels are closed. Closure of the activation gates and opening of the inactivation gates reestablish the resting condition for Na+ channels (see step 1). Diffusion of K+ through voltage-gated channels produces the afterpotential. 0 Threshold 4 –70 Time (ms) K+ K+ channels open. K+ channels closed. 5 Resting membrane potential. The resting membrane potential is reestablished after the voltage-gated K+ channels close. +35 Na+ channel K+ channels closed. Membrane potential (mV) Inactivation gate open K+ K+ channels open. 0 Threshold –70 5 Time (ms) Fig 11.12; Slide# 11-51 Refractory Period Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. • Sensitivity of area to further stimulation decreases for a time • Parts – Absolute +35 (mV) 0 Threshold –70 Absolute Relative Refractory period Time (ms) • Complete insensitivity exists to another stimulus • From beginning of action potential until near end of repolarization. No matter how large the stimulus, a second action potential cannot be produced. Has consequences for function of muscle, particularly how often a.p.s can be produced. – Relative • A stronger-than-threshold stimulus can initiate another action potential Fig 11.13; Slide# 11-52 Action Potential Frequency • Number of potentials produced per unit of time to a stimulus – Threshold stimulus: causes a graded potential that is great enough to initiate an action potential. – Subthreshold stimulus: does not cause a graded potential that is great enough to initiate an action potential. – Maximal stimulus: just strong enough to produce a maximum frequency of action I potentials. – Submaximal stimulus: all stimuli between threshold and the maximal n stimulus strength. s – Supramaximal stimulus: any stimulus stronger than a maximal stimulus. e stimuli cannot produce a greater frequency of action potentials than a These maximal stimulus. r 11-53 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Increasing frequency of action potentials (mV) +35 –55 –70 (mV) Time(ms) –55 Stimulus –70 Threshold SubThreshold threshold stimulus stimulus Submaximal stimulus Submaximal stimulus Maximal stimulus Supramaximal stimulus Increasing stimulus strength Fig 11. 14; Slide# 11-54 Propagation of Action Potentials • In an unmyelinated axon • Threshold graded current at trigger zone causes action potential • Action potential in one site causes action potential at the next location. Cannot go backwards because initial action potential site is depolarized yielding oneway conduction of impulse. 11-55 Propagation of Action Potentials Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Action potential propagation 1 Action potentials propagate in one direction along the axon. Outside of membrane becomes more negative as positive charges move away from it. Inside of membrane becomes more positive as positive charges move toward it. 2 An action potential (orange part of the membrane) generates local currents (black arrows) that tend to depolarize the membrane immediately adjacent to the action potential. 3 When depolarization caused by the local currents reaches threshold, a new action potential is produced adjacent to where the original action potential occurred. 4 Action potential propagation occurs in one direction because the absolute refractory period of the previous action potential prevents generation of an action potential in the reverse direction. Depolarization of the membrane adjacent to the site of action potential production + + – – + ++ + + + + + ––++ – – – – – – – – –– + + – – – – – – – – + + – – + ++ + + + + + + + + + – – +++ + + + – – – – + + – –– – – – – – – – + + – –– – – – + + + + – – +++ + + + + + + + + ++ – – + + + –– – – – –– + + – – – –– – – – – – + + – – – + + + + + ++ – – + + + Absolute refractory period prevents another action potential. Site of next action potential Fig. 11.15; Slide# 11-56 Continuous versus Saltatory Conduction Continuous conduction (unmyelinated fibers) – Step-by-step depolarization of each portion of the length of the axolemma • Saltatory conduction – Depolarization only at nodes of Ranvier where there is a high density of voltage-gated ion channels – Current carried by ions flows through extracellular fluid from node to node Copyright 2009 John Wiley & Sons, Inc. 57 Propagation of an Action Potential in a Neuron After It Arises At the Trigger Zone Copyright 2009 John Wiley & Sons, Inc. Diff Text 11.7; Slide# 11-58 Saltatory Conduction Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Node of Ranvier 1 An action potential (orange) at a node of Ranvier generates local currents –– (black arrows). The local currents flow ++ to the next node of Ranvier because the myelin sheath of the Schwann cell insulates the axon of the internode. Schwann cell Internode ++ –– ++ –– ++ –– ++ –– 2 When the depolarization caused by the –– local currents reaches threshold at the ++ next node of Ranvier, a new action potential is produced (orange). –– ++ ++ –– ++ –– ++ –– 1 3 Action potential propagation is rapid –– in myelinated axons because the action ++ potentials are produced at successive nodes of Ranvier (1–5) instead of at every part of the membrane along the axon. 2 –– ++ 3 –– ++ 4 –– ++ 5 –– ++ Direction of action potential propagation Fig 11.16; Slide# 11-59 Speed of Conduction • Faster in myelinated than in non-myelinated • In myelinated axons, lipids act as insulation forcing ionic currents to jump from node to node • In myelinated, speed is affected by thickness of myelin sheath • Diameter of axons: large-diameter conduct more rapidly than small-diameter. Large have greater surface area and more voltage-gated Na+ channels 11-60 Nerve Fiber Types • Type A: large-diameter, myelinated. Conduct at 15-120 m/s. Motor neurons supplying skeletal and most sensory neurons • Type B: medium-diameter, lightly myelinated. Conduct at 3-15 m/s. Part of ANS • Type C: small-diameter, unmyelinated. Conduct at 2 m/s or less. Part of ANS 11-61 11.6 The Synapse • Junction between two cells • Site where action potentials in one cell cause action potentials in another cell • Types of cells in synapse – Presynaptic – Postsynaptic 11-62 Electrical Synapses Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Cardiac muscle cell 1 Electrical synapses connect cardiac muscle cells. 1 2 An electrical synapse is a gap junction where the membranes of two cells are separated by a gap but connected by proteins called connexons. 3 An action potential (orange arrow) in the plasma membrane generates local currents (black arrows) that flow to adjacent parts of the plasma membrane and through the gap junction. 4 A local current stimulates the production of another action potential. Thus, the action potential propagates along the plasma membrane. 5 A local current flows through a gap junction and stimulates the production of an action potential in the adjacent cardiac muscle cell. Thus, the action potential propagates to the adjacent cell. Electrical synapse Connexons 2 Plasma membrane Gap junction Plasma membrane of an adjacent cell Action potential 3 Local currents 4 5 • Gap junctions that allow graded current to flow between adjacent cells. Connexons: protein tubes in cell membrane. • Found in cardiac muscle and many types of smooth muscle. Action potential of one cell causes action potential in next cell, almost as if the tissue were one cell. • Important where contractile activity among a group of cells important. Fig 11. 17; Slide# 11-63 Chemical Synapses (i.e. NMJ) • Components – Presynaptic terminal – Synaptic cleft – Postsynaptic membrane • Neurotransmitters released by action potentials in presynaptic terminal – Synaptic vesicles: action potential causes Ca2+ to enter cell that causes neurotransmitter to be released from vesicles – Diffusion of neurotransmitter across synapse – Postsynaptic membrane: when ACh binds to receptor, ligand-gated Na+ channels open. If enough Na+ diffuses into postsynaptic cell, it fires. 11-64 Chemical Synapse Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Action potential Axon 2+ Ca 1 Presynaptic terminal Synaptic vesicle Voltage-gated Ca2+ channel Synaptic cleft 2 3 Postsynaptic membrane Neurotransmitter Na+ Neurotransmitter bound to receptor site opens 4 a ligand-gated Na+ channel. 1 Action potentials arriving at the presynaptic terminal cause voltage-gated Ca2+ channels to open. 2 Ca2+ diffuse into the cell and cause synaptic vesicles to release neurotransmitter molecules. 3 Neurotransmitter molecules diffuse from the presynaptic terminal across the synaptic cleft. 4 Neurotransmitter molecules combine with their receptor sites and cause ligand-gated Na+ channels to open. Na+ diffuse into the cell (shown in illustration) or out of the cell (not shown) and cause a change in membrane potential. Fig 11.18; Slide# 11-65 Neurotransmitter Removal • Method depends on neurotransmitter/synapse. • ACh: acetylcholinesterase splits ACh into acetic acid and choline. Choline recycled within presynaptic neuron. • Norepinephrine: recycled within presynaptic neuron or diffuses away from synapse. Enzyme monoamine oxidase (MAO). Absorbed into circulation, broken down in liver. 11-66 Removal of Neurotransmitter from Synaptic Cleft Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 1 Acetylcholine molecules bind to their receptors. 2 Acetylcholine molecules unbind from their receptors. 3 Acetylcholinesterase splits acetylcholine into choline and acetic acid, which prevents acetylcholine from again binding to its receptors. Choline is taken up by the presynaptic terminal. 4 Choline is used to make new acetylcholine molecules that are packaged into synaptic vesicles. (a) Acetylcholine 1 Acetylcholine CoA Choline 2 Na+ AcetylCoA Choline 3 Acetylcholinesterase Acetic acid Norepinephrine 1 Norepinephrine binds to its receptor. 2 Norepinephrine unbinds from its receptor. 3 Norepinephrine is taken up by the presynaptic terminal, which prevents norepinephrine from again binding to its receptor. 4 Norepinephrine is repackaged into synaptic vesicles or broken down by monoamine oxidase (MAO). 4 1 4 Inactive metabolites MAO 2 Na+ 3 (b) Norepinephrine Fig 11.19; Slide# 11-67 Receptor Molecules in Synapses • Neurotransmitter only "fits" in one receptor. • Not all cells have receptors. • Neurotransmitters are excitatory in some cells and inhibitory in others. • Some neurotransmitters (norepinephrine) attach to the presynaptic terminal as well as postsynaptic and then inhibit the release of more neurotransmitter. 11-68 Neuromodulators • Chemicals produced by neurons that facilitate action potentials. Some of these act by increasing or decreasing the amount of neurotransmitter released by the presynaptic neuron. • Act in axoaxonic synapses. Axon of one neuron synapses with axon of second neuron. Second neuron is actually presynaptic. This type of connection leads to release of neuromodulators in the synapse that can alter the amount of neurotransmitter produced by the second neuron. 11-69 Postsynaptic Potentials Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 0 (mV) Threshold Resting membrane potential –70 Local depolarization (EPSP) Time (ms) (a) Excitatory postsynaptic potential (EPSP) • Excitatory postsynaptic potential (EPSP) – Depolarization occurs and response stimulatory – Depolarization might reach threshold producing an action potential and cell response • Inhibitory postsynaptic potential (IPSP) 0 (mV) Threshold Resting membrane Local hyperpolarization potential (IPSP) –70 – Hyperpolarization and response inhibitory – Decrease action potentials by moving membrane potential farther from threshold Time (ms) (b) Inhibitory postsynaptic potential (IPSP) Fig 11.20; Slide# 11-70 Presynaptic Inhibition and Facilitation • Axoaxonic synapses: axon of one neuron synapses with the presynaptic terminal (axon) of another. Many of the synapses of Presynaptic neuron CNS • Presynaptic inhibition: reduction Action potential in amount of neurotransmitter released from presynaptic terminal. Inhibitory neuron Endorphins can inhibit pain sensation by inhibiting release of Postsynaptic membrane neurotransmitters. • Presynaptic facilitation: amount (a) of neurotransmitter released from presynaptic terminal increases. Glutamate facilitating nitric oxide production Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Action potential Action potential (b) Fig 11.21; Slide# 11-71 Spatial Summation Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Axon Action potential 1 0 –50 mV –90 Time Neuron cell body Trigger zone (a) Spatial summation. Action potentials 1 and 2 cause the production of graded potentials at two different dendrites. These graded potentials summate at the trigger zone to produce a graded potential that exceeds threshold, resulting in an action potential. Axon 0 –50 Axon mV –90 Time 0 –50 mV Action potential 2 –90 Time Fig 11.22 (a); Slide# 11-72 Temporal Summation Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. (b) Temporal summation. Two action potentials arrive in close succession at the presynaptic membrane. The first action potential causes the production of a graded potential that does not reach threshold at the trigger zone. The second action potential results in the production of a second graded potential that summates with the first to reach threshold, resulting in the production of an action potential. Action potentials Trigger zone 0 –50 mV –90 T ime Fig 11.22 (b); Slide# 11-73 Combined Summation Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Inhibitory Excitatory (with temporal summation) Excitatory (c) Combined spatial and temporal summation with both excitatory postsynaptic potentials (EPSPs) and inhibitory postsynaptic potentials (IPSPs). An action potential is produced at the trigger zone when the graded potentials produced as a result of the EPSPs and IPSPs summate to reach T rigger zone Inhibitory 0 –50 mV –90 T ime Excitatory Fig 11.22 (c); Slide# 11-74 11.7 Neuronal Pathways and Circuits Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Input Output (a) Convergent pathway Input Outputs (b) Divergent pathway Input Outputs (after-discharges) (c) Reverberating circuit • Organization of neurons in CNS varies in complexity – Convergent pathways: many converge and synapse with smaller number of neurons. E.g., synthesis of data in brain. – Divergent pathways: small number of presynaptic neurons synapse with large number of postsynaptic neurons. E.g., important information can be transmitted to many parts of the brain. – Oscillating circuit: outputs cause reciprocal activation. Fig. 11. 23; Slide# 11-75 Ch. 11 Learning Objectives • After reading this chapter, students should be able to: • Explain the functions of the nervous system. • List the divisions of the nervous system and describe the characteristics of each. • Differentiate between the somatic and the autonomic nervous systems. • Contrast the general functions of the CNS and the PNS. 11-76 Ch. 11 Learning Objectives • Describe the structure of neurons and the functions of their components. • Classify neurons based on structure and based on function. • Describe the location, structure, and functions of neuroglia. • Discuss the function of the myelin sheath, and describe its formation in the CNS and in the PNS. • Distinguish between gray matter and white matter. 11-77 Ch. 11 Learning Objectives • Describe a resting membrane potential, and explain how it is created and maintained. • Explain the processes that can change the resting membrane potential. • Describe the characteristics of a graded potential. • Describe the creation of an action potential and explain how it is propagated. • Discuss the all-or-none principle as it applies to action potentials. 11-78 Ch. 11 Learning Objectives • Explain the characteristics and purpose of the refractory period. • Describe the affect of myelination on the speed of action potential propagation, as well as other factors that affect the speed of action potential conduction. • Describe the general structure and function of a synapse. • Distinguish between electrical and chemical synapses as to mode of operation and types of tissues where they are found. 11-79 Ch. 11 Learning Objectives • Describe the release of a neurotransmitter in a chemical synapse, and then its removal from the synapse. • Explain the affects of neurotransmitter binding to receptors in a chemical synapse. • Discuss the affects of neuromodulators in a chemical synapse. • Contrast excitatory and inhibitory postsynaptic potentials. • Explain the roles of presynaptic inhibition and of facilitation. 11-80 Ch. 11 Learning Objectives • Describe the processes of spatial and temporal summation. • Contrast convergent and divergent neuron pathways. • Describe an reverberating circuit. 11-81