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RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Macro electrodes

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Neurological Basis of Behavior (PSY - 610)
VU
Lesson15
RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION
Objectives:
To familiarize the students with
·  The various techniques used to study the brain and its function and structures.
·  Invasive vs. Non- Invasive methods, Stereotaxic surgery.
·  Stereotaxic Atlas used for brain surgery and manipulation,
·  Histological and cytological methods for Cell staining, Radio labelling, Flourescence,
autoradiography, Lesioning and electrical stimulation, single cell recordings, push-pull
cannulae.
·  The advanced techniques such as MRI, fMRI, CAT, PET, CT, EEG, EOG, EMG, X Ray etc
Histological, electrical chemical and pharmacological processes and techniques why so many?
·  Advanced technologies and methodologies
·  Electrophysiological methods: these are methods which measure changes of the electrical
potential and charge in the brain
Single microelectrode recording: A single thin neuron about 5-10 UM (micromolar), or a
microelectrode (1-3 UM) glass tubings or steel pens are used to record electrical potential. This is
how the all-or ­none axonal activity was measured and identified. This is also how responses to a
single stimulus single resulting in neuronal firing were first measured by Hubel and Weisel using the
visual systems of the kittens (intracellular/ extracellular recordings are possible with this technique.
Macro electrodes: These involve inserting large electrodes in large neurons. The large tips help
measure evoked potentials (EP's) of these areas, (response to a stimulus or stimulation. There are
many neurons firing in an area, and these are then magnified to a point one can hear the loud firing of
the neurons in a typical EP average evoked potential.
Surface/Scalp electrode in a region: Electroencephalography recordings are done for the human brain
and recording can show variation (during sleep) and other behaviors.
Advanced Technology:
Earlier investigations in the neurosciences were limited by the techniques available to the researcher.
Since the 1970's with the advancement of technology and the development of sophisticated equipment, it
became possible to carry out intricate experiments and measurements. These technologies which could
scan the body and brain opened up new areas of research. These are now used for research in brain
sciences and in combination with other techniques; the canvas for researchers becomes larger.
·  Contrast ­rays: The contrast X rays involves injecting part of the brain with a dye or some
substance which would block X rays. This is then contrasted with its surrounds or the lateral part
which is not injected so, basically the contrast is compared with the non injected X-Rays. This
does provide some basic information such as the location and size of a tumor in the brain or
cerebral circulatory system.
·  X-Ray Computed Axial Tomography: CAT scan was initiated in early 70's. This is a
procedure involves taking multiple X ray's from different points while the patient is lying in a
chamber and information fed to computers attached . The rotating X ray tube and detectors thus
provide the basis for the 3 dimensional images developed by computers. This method is better
than a black and white X ray which only gives very simple information; however, this cannot
measure on going changes as this is a static method.
·  Magnetic Resonance Imaging (MRI). (Resonance means echoing).The patient is placed in a
chamber of which is a highly charged magnetic field. The MRI's are high resolution images
reconstructed on the basis of waves, emitted by the hydrogen atoms after these atoms are
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Neurological Basis of Behavior (PSY - 610)
VU
activated by radio frequency waves in the magnetic field chamber. It is possible to get 2 or 3
dimensional images with MRI. Due to the high spatial resolution, MRI gives clear differences
between different loci, and tissues as is done in structural MRI. The functional MRI is used when
the brain is functioning to get images which are a clear indication of the areas where most
activity is taking place or most oxygen being used, such as testing a patient and asking him to
remember a list of words. This way we can see how different brain parts are used during
learning.
·
Positron Emission Tomography PET Brain images of ongoing brain activity rather than just
the brain structure (earlier techniques did just that). The technique of injecting radio labelled
substances such as 2-DG glucose works in combination with this technique. 2-DG glucose is
injected into the carotid artery which is taken up by the brain and, shows up in brain areas of
high activity (where glucose is normally needed). High usage would show up red (highest levels
of radioactive glucose), yellow orange, blue (least levels of glucose, therefore least activity). The
PET scan can also use blood flow, using nitricoxide (vasodilator). This shows activity and blood
usage, as wherever there is activity, there is greater blood flow. PET scans are also effective in
assessing ongoing activity
·
fMRI vs. PET
·
a) no injection needed in fMRI whereas in PET we inject radiolabeeld substances
·
b) fMRI's are both structural and functional, whereas the PET is only functional ( of varied kind
blood, glucose usage)
·
c)fMRI has clearer resolution of various parts Both techniques cannot collate
information over time ( to see how changes taking place before and after comparison)
Assays: These are procedure undertaken using various chemicals using blood urine,
extraction, and tissue of the brain (taken postmortem). There are many procedures.
·
Assays a) whole brain various metabolites are assayed post mortem. This can be done taking
the whole brain or specific brain areas to measure amount of chemicals in the areas the brain is
homogenized in the homogenizer and the chemicals and their levels measured.
·
Assays b) other assays can be carried out on the blood or urine or the Cerebrospinal fluid
(CSF). The findings that Schizophrenics urine has high levels of MHPG, a metabolite of
neurotransmitter catecholamines, indicating that they are involved in the disorder.
Neurophysiological measures There are many procedures which measure electrical activity of the
brain and other tissues to give us an assessment of the working of these areas.
·
EEG: Electroencephalography: This gives us an idea of the ongoing electrical activity in the
brain.  Scalp electrodes are placed at various locations (temporal, frontal, occipital, and
parietal) to get a recording of the electrical charge and electrical activity of the different parts at
the same time. These electrodes pick the electrical signals and then these are sent to a magnifier
where they can be seen on the oscilloscope. Though this does not give us a clear idea of how
each neuron is working, but the general patterns are consistent and have been shown across
species. For example, the sleep state recording would show us when a person or animal enters
deep sleep the recording show Low frequency, high amplitude waves (1-3 cycles per second).
·
EOG Electro-oculograph: These measure the electrical activity of eye muscles to monitor the
eye movement using electrodes placed on the eyes. This is most effective in sleep studies
where Rapid Eye Movement ( REM) sleep stage can be seen through changes in EOG activity.
This works well with the EEG recordings to study sleep.
·
EMG: Electromyograph: Measuring electrical activity of the muscle. In this procedure
electrodes are placed on the muscle that we are measuring. The muscular tension/ tone of the
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Neurological Basis of Behavior (PSY - 610)
VU
neck muscles is also measured in sleep and is a very good indicator of the changes form Non
REM to REM sleep.
·
Polygraphic recording For measuring electrical skin conductance along with other measures
such as Blood pressure, Pulse rate, and breathing is measured as an orchestrated response,
Reference
1. Kalat J.W (1998) Biological Psychology Brooks/ Cole Publishing
2. Carlson N.R. (2005) Foundations of Physiological Psychology Allyn and Bacon, Boston
3. Pinel, John P.J. (2003) Biopsychology (5th edition) Allyn and Bacon Singapore
4 Bloom F, Nelson and Lazerson (2001), Behavioral Neuroscience: Brain, Mind and Behaviors (3rd
edition) Worth Publishers New York
5. Bridgeman,B (1988)The Biology of Behaviour and Mind. John Wiley and Sons New York
6. Seigel,G.J. ( Ed. in chief) Agranoff, B.W, Albers W.R. and Molinoff, P.B. (Eds) Basic
Neurochemistry: Molecular, Cellular and Medical Aspects.
7. Brown,T.S. And Wallace. (1980) P.M Physiological Psychology
Academic Press New York
Note: References #2, 3, and 4 are followed most closely, as they have been used in teaching as well;
further individual references/pages are also given on the power points of each lesson.
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Table of Contents:
  1. INTRODUCTION:Descriptive, Experimental and/ or Natural Studies
  2. BRIEF HISTORICAL REVIEW:Roots of Behavioural Neurosciences
  3. SUB-SPECIALIZATIONS WITHIN THE BEHAVIORAL NEUROSCIENCES
  4. RESEARCH IN BEHAVIOURAL NEUROSCIENCES:Animal Subjects, Experimental Method
  5. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Species specific
  6. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Decent With Modification
  7. EVOLUTIONARY AND GENETIC BASIS OF BEHAVIOUR:Stereoscopic vision
  8. GENES AND EXPERIENCE:Fixed Pattern, Proteins, Genotype, Phenotypic
  9. GENES AND EXPERIENCE:Mendelian Genetics, DNA, Sex Influenced Traits
  10. GENES AND EXPERIENCE:Genetic Basis of behavior, In breeding
  11. GENES AND EXPERIENCE:Hybrid vigor, Chromosomal Abnormalities
  12. GENES AND EXPERIENCE:Behavioral Characteristics, Alcoholism
  13. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION
  14. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Activating brain
  15. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Macro electrodes
  16. RESEARCH METHODS AND TECHNIQUES OF ASSESSMENT OF BRAIN FUNCTION:Water Mazes.
  17. DEVELOPMENT OF THE NERVOUS SYSTEM:Operation Head Start
  18. DEVELOPMENT OF THE NERVOUS SYSTEM:Teratology studies, Aristotle
  19. DEVELOPMENT OF THE NERVOUS SYSTEM:Stages of development, Neurulation
  20. DEVELOPMENT OF THE NERVOUS SYSTEM:Cell competition, Synaptic Rearrangement
  21. DEVELOPMENT OF THE NERVOUS SYSTEM:The issues still remain
  22. DEVELOPMENT OF THE NERVOUS SYSTEM:Post natal
  23. DEVELOPMENT OF THE NERVOUS SYSTEM:Oxygen level
  24. Basic Neuroanatomy:Brain and spinal cord, Glial cells, Oligodendrocytes
  25. Basic Neuroanatomy:Neuron Structure, Cell Soma, Cytoplasm, Nucleolus
  26. Basic Neuroanatomy:Control of molecules, Electrical charges, Proximal-distal
  27. Basic Neuroanatomy:Telencephalon, Mesencephalon. Myelencephalon
  28. Basic Neuroanatomy:Tegmentum, Substantia Nigra, MID BRAIN areas
  29. Basic Neuroanatomy:Diencephalon, Hypothalmus, Telencephalon, Frontal Lobe
  30. Basic Neurochemistry:Neurochemicals, Neuromodulator, Synaptic cleft
  31. Basic Neurochemistry:Changes in ionic gates, The direct method, Methods of Locating NT
  32. Basic Neurochemistry:Major Neurotransmitters, Mesolimbic, Metabolic degradation
  33. Basic Neurochemistry:Norepinephrine/ Noradrenaline, NA synthesis, Noadrenergic Pathways
  34. Basic Neurochemistry:NA and Feeding, NE and self stimulation: ICS
  35. Basic Neurochemistry:5HT and Behaviors, Serotonin and sleep, Other behaviours
  36. Basic Neurochemistry:ACH and Behaviors, Arousal, Drinking, Sham rage and attack
  37. Brain and Motivational States:Homeostasis, Temperature Regulation, Ectotherms
  38. Brain and Motivational States:Biological Rhythms, Circadian rhythms, Hunger/Feeding
  39. Brain and Motivational States:Gastric factors, Lipostatic theory, Neural Control of feeding
  40. Brain and Motivational States:Resting metabolic state, Individual differences
  41. Brain and Motivational States:Sleep and Dreams, Characteristics of sleep
  42. Higher Order Brain functions:Brain correlates, Language, Speech Comprehension
  43. Higher Order Brain functions:Aphasia and Dyslexia, Aphasias related to speech
  44. Higher Order Brain Functions:Principle of Mass Action, Long-term memory
  45. Higher Order Brain Functions:Brain correlates, Handedness, Frontal lobe