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PSY3010S - Research in Neuropsychology.pdf

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‭The Cell Doctrine‬ ‭WEEK ONE:‬‭Research in Neuropsychology‬ ‭‬ ‭Galen (130 - 201 AD)‬‭-‬‭Ventricular Localization Hypothesis‬‭(first anatomical‬...

‭The Cell Doctrine‬ ‭WEEK ONE:‬‭Research in Neuropsychology‬ ‭‬ ‭Galen (130 - 201 AD)‬‭-‬‭Ventricular Localization Hypothesis‬‭(first anatomical‬ ‭theory)‬ ‭ esearch Methods One‬ R ‭-‬ ‭Mental and spiritual processes arise reside in brain’s ventricles‬ ‭What is neuropsychology‬ ‭-‬ ‭Early attempt to localize mental function‬ ‭-‬ ‭Later known as The Cell Doctrine (innacurate)‬ ‭Earliest Discoveries‬ ‭Anatomical Discoveries and Spiritual Soul‬ ‭‬ ‭Trephination (Stone Age)‬ ‭‬ ‭Andres Vesalius (1514-1564):‬‭Shift away from Ventricular‬‭Theory‬‭(founder of‬ ‭-‬ ‭Form of brain surgery‬ ‭human anatomy)‬ ‭-‬ ‭Drill holes through the skull to relieve pressure‬ ‭-‬ ‭Overall structure and mass mediate mental processes‬ ‭-‬ ‭Reasons:‬ ‭-‬ ‭Groundwork for a more integrated understanding of brain function‬ ‭1.‬ ‭Medical Emergency‬ ‭2.‬ ‭“Magical” form of healing (eg epilepsy or schizophrenia)‬ ‭‬ R ‭ ene Descartes (1596-1650):‬‭Mind-Body Dualism‬‭(first‬‭understanding of mental‬ ‭-‬ ‭Similar procedures were done today‬ ‭health)‬ ‭-‬ ‭Split between mental processes and physical abilities‬ ‭-‬ ‭Pineal gland control center of mind and body - unique because there is only‬ ‭one and it is in the middle of brain‬ ‭Ancient Greek Perspectives‬ ‭‬ ‭Hippocrates (460-377BCE):‬‭Brain Hypothesis‬‭(idea that‬‭brain is source of all‬ ‭behaviour)‬ ‭-‬ ‭Brain controls senses and movements‬ ‭-‬ ‭Understood contralateral control‬ ‭-‬ ‭Emotions arise in the brain‬ ‭-‬ ‭Behaviour is not divinely controlled but rather medical‬ ‭‬ ‭Plato (420-347 BCE):‬‭Tripartite Soul Concept‬ ‭-‬ ‭Soul divided into reason, spirit, and appetite‬ ‭-‬ ‭Reason arises in the brain‬ ‭‬ ‭Aristotle (384-322 BCE):‬‭Cardiac Hypothesis‬ ‭-‬ ‭The heart is the seat of thought and emotion‬ ‭Localization Theory‬ ‭Integrated Theories‬ ‭‬ ‭Franz Gall (1758 -1828):‬‭Localization Theory and Phrenology‬ ‭‬ ‭Hughlings Jackson (1835-1911): Jackson’s functional model‬ ‭-‬ ‭Localization theory:‬ ‭-‬ ‭Higher mental function composed of simpler functions‬ ‭Brain composed of independent organs, each responsible for specific‬ ‭-‬ ‭Hierarchical organization of brain:‬ ‭personality or cognitive trait‬ ‭‬ ‭Lower levels = basic functions‬ ‭-‬ ‭Phrenology:‬ ‭‬ ‭Higher levels = complex thought and behaviour‬ ‭Personality and cognitive traits determined by size of brain area/shape of‬ ‭-‬ ‭Damage to higher levels result in “dissolution” of complex functions, revert to‬ ‭skull (size of brain area = amount of skill in that area)‬ ‭basic functions‬ ‭Era of Cortical Localization‬ ‭‬ ‭Alexander Luria (1902-1977): Luria’s Functional Model‬ ‭‬ ‭Paul Broca (1824-1880)‬‭Localization of expressive‬‭language‬ ‭-‬ ‭CNS Divided Into Units:‬ ‭-‬ ‭Production of language localized to region of the left frontal lobe‬ ‭‬ ‭Unit 1: brainstem and associated areas = regulate arousal and‬ ‭‬ ‭Carl Wernicke (1848-1904)‬‭Localization of receptive‬‭language‬ ‭maintain muscle tone‬ ‭-‬ ‭Understanding language is localized to region of the left temporal lobe‬ ‭‬ ‭Unit 2: posterior areas of cortex = reception, integration, and analysis‬ ‭of sensory information‬ ‭‬ ‭Unit 3: frontal and prefrontal lobe = planning, executing and verifying‬ ‭behaviour‬ ‭-‬ ‭Behaviours have unique functional systems, each have unique pattern of‬ ‭interaction among units‬ ‭-‬ ‭Pluripotentiality‬‭: one neural structure can fulfill‬‭multiple functions, depending‬ ‭on the functional network and pattern of co-activations displayed at any given‬ ‭time‬ ‭Critique of Localization Theory‬ ‭-‬ ‭Plasticity‬‭: the ability of the brain to change or‬‭reorganize the functioning of its‬ ‭‬ ‭Sigmund Freud (1856-1938)‬‭Complex Networks in Brain‬ ‭structures and neural mechanisms‬ ‭-‬ ‭Cognitive function involves complex networks of regions in the brain‬ ‭-‬ ‭Need to understand connectivity and interactions to understand behaviour‬ ‭(Relatively) Modern Neuropsychology‬ ‭and cognition‬ ‭‬ ‭Technological advancements (eg. neuroimaging)‬ ‭‬ ‭Expansion of research areas (eg. cognitive neuroscience)‬ ‭Localization vs Equipotentiality‬ ‭‬ ‭Henry Hecaen (1912 - 1983)‬ ‭‬ ‭Pierre Flourens (1794-1867):‬‭Equipotential theory‬ ‭-‬ ‭Demonstrated functional properties of the RH‬ ‭-‬ ‭Brain regions have potential to carry out most functions‬ ‭‬ ‭Arthur Benton (1902 - 2007)‬ ‭-‬ ‭Regions can compensate for damaged areas‬ ‭-‬ ‭Developed neuropsychological measures for RH‬ ‭‬ ‭Karl Lashley (1890-1958):‬‭Principle of mass action‬ ‭‬ ‭Oliver Zangwill (1913 - 1987)‬ ‭-‬ ‭Each part of brain participates in more than one function‬ ‭-‬ ‭Showed language in left-handed people may be localized to the RH‬ ‭-‬ ‭Extent of behaviour impairment is directly proportional to mass of removed‬ ‭‬ ‭Norman Geschwind (1927 - 1984)‬ ‭tissue‬ ‭-‬ ‭Behavioural disturbances due to disconnections between brain pathways‬ ‭‬ ‭Muriel Lezak (1970s)‬ ‭-‬ ‭Pioneered the assessment approach in neuropsychology‬ ‭ esearch Methods 2‬ R ‭Structural Imaging‬ ‭Neurohistory‬ ‭ ‬ ‭used to quantify brain structure‬ ‭‬ ‭Definition: Study of the microscopic structure of brain tissue‬ ‭‬ C ‭ heaper and more widely available‬ ‭‬ ‭Key techniques:‬ ‭-‬ ‭Golgi stain: visualizes entire neurons - including dendrites and axons‬ ‭X-Ray (late 1970s)‬ ‭-‬ ‭Nissl stain: highlights cell bodies‬ ‭‬ ‭What it is:‬ ‭‬ ‭Uses and significance:‬ ‭-‬ ‭Visualize skull and large abnormalities in brain‬ ‭-‬ ‭Investigating neuronal organization and connectivity‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Diagnosing brain tissue abnormalities‬ ‭-‬ ‭Electromagnetic waves are absorbed at different rates by different tissues‬ ‭Nissl stain‬ ‭-‬ ‭Dense structures, like bone, absorb more X-rays and appear white on image‬ ‭‬ ‭What it is:‬ ‭-‬ ‭Less dense structures, like tissue, appear darker‬ ‭-‬ ‭Visualization of cell body and nucleus of neuron‬ ‭‬ ‭Application:‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Quickly assess bone injuries and detect major tumors or large bleeds‬ ‭-‬ ‭Uses simple dyes‬ ‭‬ ‭Advantage:‬ ‭‬ ‭Uses:‬ ‭-‬ ‭Universally available technology‬ ‭-‬ ‭Study neuronal density‬ ‭-‬ ‭Inexpensive‬ ‭-‬ ‭Study arrangement of neurons in different brain regions‬ ‭-‬ ‭Good visualization of the skull (works for skull fractures)‬ ‭-‬ ‭Helps with pathology (can’t see cell body if axon is injured)‬ ‭‬ ‭Disadvantage:‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Radiation exposure can destroy diseased tissue‬ ‭-‬ ‭Limited structural information‬ ‭-‬ ‭2D images‬ ‭-‬ ‭Technical variability‬ ‭-‬ ‭Little differentiation between bone and CSF‬ ‭Golgi stain‬ ‭‬ ‭What it is:‬ ‭-‬ ‭Visualization of entire neuron (cell body, dendrites, axons)‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Uses silver chromate to stain individual neurons‬ ‭‬ ‭Uses:‬ ‭-‬ ‭Study complete structure of neuron‬ ‭-‬ ‭Study complex networks and connections between cells‬ ‭-‬ ‭Understand intricate wiring of the brain by mapping distribution of axons and‬ ‭dendrites‬ ‭-‬ ‭Identify neuron types‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Selective staining: Only stains small percentage of neurons‬ ‭-‬ ‭Can only be used on dead tissue‬ ‭-‬ ‭Complex preparation: staining process is technically demanding‬ ‭-‬ ‭Cannot see inner structure‬ ‭CT Scan‬ ‭MRI‬ ‭‬ ‭What it is:‬ ‭‬ ‭What it is:‬ ‭-‬ ‭Provides cross-sectional images of the brain‬ ‭-‬ ‭Highly detailed image of the brain‬ ‭‬ ‭How it works:‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Machine sends X-ray beams through body from multiple angles‬ ‭-‬ ‭Machine uses magnets to align the hydrogen atoms in body‬ ‭-‬ ‭X-ray detectors on the opposite side of machine measure the amount of‬ ‭-‬ ‭Radio wave sent through, knocking the hydrogen atoms out of alignment‬ ‭X-rays that pass through body‬ ‭-‬ ‭When the radio wave is turned off, hydrogen atoms realign and send out‬ ‭-‬ ‭Data sent to computer and computer creates image‬ ‭signals‬ ‭‬ ‭Uses:‬ ‭-‬ ‭Machine detects these signals and a computer turns them into detailed‬ ‭-‬ ‭Determine presence of lesions,‬ ‭images‬ ‭-‬ ‭structural deviations, and tumors‬ ‭‬ ‭Uses:‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Determine presence of lesions,‬ ‭-‬ ‭Quick (±10-15 minutes)‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Inexpensive‬ ‭-‬ ‭Safer for repeated exposure (no radiation)‬ ‭-‬ ‭Widely used in research‬ ‭-‬ ‭Highly detailed images (more sensitive, better for diagnosis)‬ ‭-‬ ‭Quiet‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Good for emergencies‬ ‭-‬ ‭Long (±30-60 minutes)‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭expensive‬ ‭-‬ ‭Poor resolution of grey and white matter structures‬ ‭-‬ ‭Uncomfortable due to‬ ‭-‬ ‭No information about function‬ ‭-‬ ‭enclosed space and loud noises‬ ‭-‬ ‭Harmful with excessive exposure‬ ‭-‬ ‭structural deviations, and tumors‬ ‭Research Methods 3‬ ‭PET (Positron Emission Tomography)‬ ‭ unctional Neuroimaging‬ F ‭‬ ‭What it is:‬ ‭ ‬ ‭the use of neuroimaging technology to measure an aspect of brain function‬ ‭-‬ ‭Imaging technique that visualizes metabolic processes in the brain‬ ‭-‬ ‭Uses radioactive tracers to detect functional changes in brain tissue‬ ‭fMRI (Functional Magnetic Resonance Imaging)‬ ‭‬ ‭How it works:‬ ‭‬ ‭What is it:‬ ‭-‬ ‭Radiotracer (usually glucose) injected‬ ‭-‬ ‭Measures brain activity by detecting changes in blood flow‬ ‭-‬ ‭Tracer accumulates in areas with high metabolic activity‬ ‭‬ ‭How it works:‬ ‭-‬ ‭As tracer is metabolized, they emit gamma rays‬ ‭-‬ ‭Blood-Oxygen-Level Dependent (BOLD) Signal:‬ ‭-‬ ‭Gamma rays are detected and computer generates image showing metabolic‬ ‭‬ ‭Increased neuronal activity > increased blood flow > higher oxygen‬ ‭activity‬ ‭levels > stronger MRI signal‬ ‭‬ ‭Uses:‬ ‭‬ ‭Uses:‬ ‭-‬ ‭Studying brain metabolism, blood flow, and neurotransmitter activity‬ ‭-‬ ‭Brain mapping: identifies areas of the brain involved in specific functions‬ ‭-‬ ‭diagnosing and monitoring neurological disorders‬ ‭-‬ ‭Patient performs a task during the process‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Clinical use: pre-surgical planning, understanding brain disorders‬ ‭-‬ ‭Functional imaging: provides information on brain function and metabolism‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Early detection: can detect abnormalities before structural changes occur‬ ‭-‬ ‭Non-invasive: no need for injections or radiation‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭High Spatial Resolution: detailed images of brain activity‬ ‭-‬ ‭Radiation exposure‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Cost and availability‬ ‭-‬ ‭Temporal resolution: slower compared to electrical activity measurements like‬ ‭EEG‬ ‭-‬ ‭Motion sensitive: patient must remain still during the scan‬ ‭SPECT (Single Phonton Emission Computed Tomography)‬ ‭Electrophysiological Procedures‬ ‭‬ ‭What it is:‬ ‭EEG (Electroencephalography)‬ ‭-‬ ‭Imaging technique that visualizes blood flow and activity in the brain‬ ‭‬ ‭What it is:‬ ‭-‬ ‭Uses radioactive tracers to detect functional changes in the brain tissue‬ ‭-‬ ‭Records electrical activity of the cortex‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Measures brain waves and patterns‬ ‭-‬ ‭Radioatracer injection‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Tracer uptake‬ ‭-‬ ‭Electrodes detect electrical signals produced by neurons‬ ‭-‬ ‭Detection‬ ‭-‬ ‭Signals amplified and recorded by a computer‬ ‭‬ ‭Uses:‬ ‭-‬ ‭Different brain wave patterns (e.g. alpha, beta, delta, theta) are analysed‬ ‭-‬ ‭Diagnosing and monitoring neurological conditions‬ ‭‬ ‭Uses‬ ‭‬ ‭Advantage:‬ ‭-‬ ‭Diagnosing and monitoring epilepsy and sleep disorders‬ ‭-‬ ‭Functional imaging: provides information on blood flow and brain activity‬ ‭-‬ ‭Monitoring brain activity during anesthesia and surgery‬ ‭-‬ ‭Less expensive‬ ‭‬ ‭Advantages:‬ ‭‬ ‭Limitation:‬ ‭-‬ ‭Non-invasive‬ ‭-‬ ‭Radiation exposure‬ ‭-‬ ‭High temporal resolution: can capture rapid changes in brain activity‬ ‭-‬ ‭Lower spatial resolution compared to PET‬ ‭-‬ ‭Real-time monitoring‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Limited spatial resolution:‬ ‭-‬ ‭limited ability to pinpoint the location of brain activity‬ ‭-‬ ‭Requires a controlled environment to avoid external electrical interference‬ ‭EP’s (Evoked Potentials)‬ ‭‬ ‭What is it:‬ ‭-‬ ‭Measures brain’s response to specific stimuli‬ ‭-‬ ‭Types: auditory, visual, somatosensory‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Specific stimuli are presented to patient while electrodes record brain activity‬ ‭-‬ ‭Electrical responses represent the timing and strength of neuronal pathways‬ ‭‬ ‭Applications:‬ ‭-‬ ‭Assesses sensory pathway integrity‬ ‭-‬ ‭Diagnosing & monitoring multiple sclerosis and other neurological conditions‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Specific‬ ‭-‬ ‭Objective measurement‬ ‭-‬ ‭Non-invasive‬ ‭‬ ‭Disadvantages:‬ ‭-‬ ‭Requires specialized equipment and expertise‬ ‭-‬ ‭Limited specificity: does not provide detailed anatomical information‬ ‭-‬ ‭Requires controlled environment‬ ‭Cerebrospinal Fluid Studies‬ ‭Cerebrospinal Fluid‬ ‭‬ ‭What is it:‬ ‭-‬ ‭CSF studies involve analysing the fluid that surrounds the brain and spinal‬ ‭cord‬ ‭‬ ‭How it works:‬ ‭-‬ ‭Lumbar puncture/spinal tap‬ ‭‬ ‭Applications:‬ ‭-‬ ‭Diagnosing neurological conditions (e.g. infections, abnormal proteins)‬ ‭‬ ‭Advantages:‬ ‭-‬ ‭Detailed diagnostic information: comprehensive data on chemical and cellular‬ ‭composition of CSH‬ ‭-‬ ‭Direct access to CNS: allows for direct precise diagnosis‬ ‭‬ ‭Limitations:‬ ‭-‬ ‭Invasive: procedure can be uncomfortable and carries risks such as‬ ‭headache, bleeding or infection‬ ‭-‬ ‭Procedure time: takes longer and requires more preparation‬

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