BIO AND COG WEEK 2 Flashcards

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1
Q

SYNAPTIC TRANSMISSION AND NEUROPHARAMACOLOGY

A
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2
Q

what can neurotransmitters be?

A
  • Excitatory- allow sodium to flow into the postsynaptic neuron
  • inhibitory- allow chloride to flow into the postsynaptic neuron
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3
Q

what are the seven processes in neurotransmitter action?

A

1- Neurotransmitter molecules are synthesized from precursors under the influence of enzymes

2- neurotransmitters molecules are stored in vesicles

3- neurotransmitter molecules that leak from their vesicles are destroyed by enzymes

4- then action potentials cause vesicles to fuse with the presynaptic membrane and release their neurotransmitter molecules into the synapse

5- then the released neurotransmitter molecules bind with auto receptors and inhibit subsequent neurotransmitter release.

6- Then the released neurotransmitter molecules bind to postsynaptic receptors

7- thus the released neurotransmitter molecules are deactivated either by reuptake or enzymatic degrdation.

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4
Q

what are the four categories of neurotransmitter?

A
  • Amino acids- Molecular subcomponents of proteins e.g glutamate, GABA, glycine
  • Monoamines- synthesised from an amino acids e.g. dopamine ,noradrenaline, adrenaline,serotonin,
    histamine

peptides- shorts chains of amino acids- e.g oxytocin, somatostatin opioids

others- other organic or inorganic molecules
e.g acetylcholine, adenosine and nitric oxide

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5
Q

what are some amino acid neurotransmitter pathways ?

A
  • glutamate- the most prevalent excitatory neurotransmitter
    (glutamatergic pathways)

Gaba- the most prevalent inhibitory neurotransmitter
(GABAergic pathways)

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6
Q

whats functions does dopamine pathways have?

A
  • IN THE FRONTAL CORTEX
  • Functions
  • Reward(motivation)
  • pleasure,euphoria
  • motor function
  • compulsion
  • perseveration
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7
Q

what function does serotonin pathways do?

A
  • IN THE STRIATUM , SUBSTANTIA NIGRA

function

  • mood
  • memory
  • processing
  • sleep
  • cognition
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8
Q

HOW DO PHARMACOLOGICAL AGENTS WORK ON THE BRAIN?

A
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9
Q

what does direct and indirect binding mean?

A

DIRECT- binding to the neurotransmitter binding site

INDIRECT- the neurotransmitter binds elsewhere

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10
Q

what are the names of the two agents?

A
  • AGONIST- a drug tat increases the effect of a neurotransmitter
  • Antagonist - a drug that decreases the effect of a neurotransmitter
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11
Q

Describe the agonistic drug effect processes?

A

1- drug increases the synthesis of neurotransmitter molecules e.g by increasing the amount of precursor.

2- the drug then increases the number of neurotransmitter molecules by destroying degrading enzymes

3 - thus increasing the release of neurotrasmitter molecules from terminal buttons

4- then the drug binds to postsynaptic receptors and blocks their inhibitory effect on neurotransmitter release

5- then the drug binds to postsynaptic receptors and either activates them or increases the effect on them of neurotransmitter molecules

6- then the drug blocks the deactivation of neurotransmitter molecules by blocking degradation or reuptake

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12
Q

what are the antagonistic drug effect processes ?

A

1- the drug blocks the synthesis of neurotransmitter molecules e.g by destroying synthesizing enzymes

2- the drug then causes neurotransmitter molecules to leak from the vesicles and be destroyed by degrading enzymes

3- The drug then blocks the release of the neurotransmitter molecules from terminal buttons

4- the drug then activates auto receptors and inhibits neurotransmitter release

5- due to the drug being a receptor blocker it binds to the postsynaptic receptors and blocks the effect of the neurotransmitter

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13
Q

what is CURARE?

A
  • an arrow poison
  • a direct acetylcholine antagonist
  • it blocks a subtype of the acetylcholine receptor at neuromuscular junctions by binding to the site where the neurotransmitter should
  • results in complete paralysis ( death results from asphyxia)
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14
Q

what is FLUOXETINE?

A
  • known as Prozac- antidepressant
  • a SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRI)
  • ensures that endogenous serotonin remains in the synaptic cleft for longer by blocking this channel
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15
Q

APPROACHES TO STUDYING THE BRAIN

A
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16
Q

Describe MRI?

A
  • uses a strong magnetic field and radio waves to produce an image of the brain based on hydrogen ions in the body
  • used to produce several kinds of image
17
Q

describe functional - fmri ?

A
  • uses mri scanner to measure task related changes in blood flow
  • measures the protons which are released when the haemoglobin in oxygenated blood releases its oxygen in the working brain
  • highly correlated with brain activity levels
18
Q

what are the strengths and weaknesses of MRI and fMRI?

A

MRI

  • high spatial resolution
  • can discern brain structure

fmri
- low temporal resolution - because it relies on the changes7 in blood flow that occur in response to the stimulus
-

19
Q

which techniques are invasive or non invasive ?

A

non invasive

  • EEG
  • MEG

invasive

  • ECoG
  • SEEG
20
Q

describe the features of ECoG and intracortical?

A
  • only done on humans in the case of medical need
  • recordings are relatively hard to come by and only done on atypical brains
  • THEY HAVE EXQUISITE TEMPORAL AND SPATIAL RESOLUTION
21
Q

What are the strengths and weaknesses of EEG?

A
  • EEG =excellent temporal resolution - directly measuring the electrical activity in the brain ( miliseconds)
  • poor spatial resolution because signals has to pass through several insulating layers before it reaches the electrodes
22
Q

describe MEG

A
  • The brains electrical currents are associated with magnetic fields
  • highly sensitive sensors in the MEG system record the magnetic fields from outside the head.
  • better spatial resolution that EEG
23
Q

what can you measure EEG and MEG?

A
  • brain oscillations - specific oscillations in specific areas cortex reflect particular function

e.g - alpha in occipital lobe
=visual processing and attention

theta= in the frontal lobe
- memory
beta above motor cortex
= planning and execution of movements

24
Q

what are the strength and weaknesses of MEG and EEG ?

A
  • both= excellent temporal resolution =direct measures of the electrical activity in the brain
  • weakness= EEG- poor spatial resolution = insulating effects of the intervening tissues

strength= MEG- great spatial resolution= magnetic fields pass through these tissues

25
Q

Name some examples Antagonists and agonists?

A

Antagonists= fenclonine (PCPA) = prevents enzymes from adding = used in symptoms of certain tumours.
- reserpine

Agonists= MAO inhibitor= blocks enzyme called monoamine oxidise which converts dopamine to an inactive substance in the pre-synaptic neuron

COMPETITIVE ANTAGONISTS= Naloxone= binds to any opioids receptors at the same site as the opioid would preventing it from binding.

DIRECT AGONISTS= morphine binds to …-opioids receptors in brain and fully activates them.= decreases feeling of pain.