Unit 2 Flashcards

1
Q

What does the positive membrane potential (Nav, Kv) cause to open…

A

open voltage gated calcium channels
(densely located at terminal)

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2
Q

Calcium binds with proteins on the surface of the vesicle and activates them. What does this do?

A

the proteins allow vesicles to fuse with cell membrane (of PREsynaptic neuron) and release their contents (NT) into synapse

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3
Q

In order to release neurotransmitters, we need what to enter the cell?

A

CALCIUM

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4
Q

Do neurotransmitter pass through channels?

A

NOOOOOO
-bind to receptors that are connected to channels that then open allowing flow of ions

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5
Q

3 ways of removing Neurotransmitters

A
  1. Reuptake
  2. Enzymatic Degradation
  3. Diffusion
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6
Q

Reuptake

A

pre-synaptic terminal sucks it up and repackages it for reuse

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7
Q

enzymatic degradation

A

special enzymes in synapse destroy it

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8
Q

diffusion

A

-it slowly moves out of synapse
-concentration gradient (nt diffuse from area of high concentration to low concentration)

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9
Q

Glutamate

A

-amino acid
-most abundant excitatory NT
-binds to ligand gated Na+ channel (causes EPSP)

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10
Q

GABA

A

-amino acid
-most abundant inhibitory NT
-binds to ligand gated Cl- channel (causes IPSP)

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11
Q

Monomines
-indolamines

A

seratonin

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12
Q

Catecholamines

A

-dopamine
-norepinephrine
-epinephrine

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13
Q

Acetylcholine

A

-released at the neuromuscular junction from motorneuron
-neurons that release this are called CHOLINERGIC NEURONS

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14
Q

Affinity

A

the strength and likelihood of NT binding with receptor
-high affinity=higher binding likelihood and strength
ex. dopamine receptors have a high affinity for dopamine

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15
Q

Receptors come in two forms:

A

Iontropic receptors
Metabotropic receptors

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16
Q

Iontropic receptors

A

ligand gated channel
-when NT binds to a channel the channel opens

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17
Q

Iontropic receptors
-Glutamate receptors

A

1st AMPA- when glutamate binds with the AMPA receptor it causes the opening of Na+ channels
2nd NMDA- Has magnesium ion blocking the flux of ions through channel
-an action potential will depolarize the membrane and cause the removal of magnesium
-now when glutamate binds to receptor AGAIN, calcium can flow through channel into cell

18
Q

Activation of both AMPA NMDA coupled channel will…

A

Increase the length of an EPSP ALOT

19
Q

Iontropic receptors
-GABA receptors

A

-bound to inotropic Cl- channel
-causes IPSP on postsynaptic cell
ex. alcohol and Xanax (allosteric modulators of the receptor)

20
Q

Metabotropic receptors

A

DO NOT have channel
-when a NT binds a 2nd protein is related into cell (G PROTEIN)
-effects are much slower than ionotropic

21
Q

GPCRs to know

A

Gq
Gs
Gi

22
Q

Gq

A

=excitatory
-increase levels of IP3 causing release of calcium

23
Q

Gs

A

=excitatory
-increase levels of CAMP
-activates adenylyl

24
Q

Gi

A

=inhibitory
-decreases levels of cAMP
-inhibits adenylyl

25
Q

Autoreceptors

A

receptors that exit on the presynaptic membranes
-think of it as monitoring system
-stops release of the NT being released

26
Q

Pharmacology

A

the study of drug origins, effects, and mechanisms of action
-drugs can exert their physiological effects by binding with receptors

27
Q

Psychotropic drugs must reach…

A

THE BRAIN
-cross blood brain barrier
-have multiple targets not just one

28
Q

endogenous

A

=already existing in your body
-each drug alters endogenous signaling cascades
ex. your body produces the NT serotonin, drugs can influence dopamine signaling

29
Q

agonists

A

a drug that binds with and ACTIVATES an endogenous receptor or signaling process

30
Q

antagonists

A

a drug that binds with and BLOCKS the actions of an endogenous receptor or signaling process
-ketamine is an NMDA receptor antagonist (psychedelics and ketamine are suggested to have antidepressant effects)

31
Q

modulators

A

CHANGE the way a receptor function, increasing or decreasing the effectiveness of the normal ligand
ex. alcohol changing GABA receptors

32
Q

Drug metabolism

A

drug molecules get “broken down” by enzymes in your blood
-terminate ability for any psychiatric affect
-chopped up into METABOLITES

33
Q

What enzyme breaks down 5HT (serotonin) and psilocin

A

Monoamine oxidase breaks down 5HT and psilocin
-liver is primary source of these enzymes

34
Q

Drugs and their metabolites

A

-Active drug —> inactive metabolite (most common)
-Inactive drug —> active drug (psilocybin to psilocin)
-Active drug —> active metabolite (heroin and morphine), (prolongs drug actions)

35
Q

tryptamine

A

Psilocybin/psilocin, DMT
type of psychedelic
-5HT2A receptor agonist

36
Q

addition

A

drugs in the same class share targets
ex. alcohol and Xanax both affect GABA

37
Q

Subtraction

A

drugs may have opposing effects
ex. using Naloxone (narcan) to stop heroin overdose

38
Q

some tryptamine psychedelics require “activation”
for example…

A

psilocybin cannot permeate the blood brain barrier and binds with low affinity to the 5HT2A receptor
-psilocybin —-> psilocin in order to affect brain

39
Q

Duration of drug action depends on…

A
  1. Amount of drug +route of administration
  2. affinity for receptor and availability
  3. ability for drug to “resist” enzymatic degradation
  4. the set of the individual
40
Q

Set=
Setting=

A

set= everything about the individual (age, genetics, etc.)
setting= where (clinic, at home, etc)

41
Q

Psychedelics act at the level…

A

5HT2A receptor
-5HT2A is Gq coupled !!!!!

42
Q
A