Psychopharmacology Flashcards

1
Q

Synaptic weighting

A
  • conserves energy
  • weaker connections can be pruned
  • stronger connections get delegated work
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2
Q

Reciprocal inhibition

A
  • happens on a network level
  • if network 1 is excitatory network 1 inhibits network 2 which is inhibitory, making it unable to inhibit
  • conserves energy
  • example of a phasic change
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3
Q

Post inhibitory rebound

A
  • when reciprocal inhibition happens network 2 is easier to excite because it was inhibited
  • after being inhibited there is increased excitability
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4
Q

Pharmacokinetics

A
  • medications for mental disorders are based on pH (absorption)
  • how to get to the target/brain –> has to pass blood-brain barrier (distribution)
  • how long the drug will stay in the system
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5
Q

Affinity

A

how sterically available the drug is for its binding site

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6
Q

Potency

A

how much of the drug does it take to get the action

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7
Q

Efficacy

A

how well the drug does what it is intended to do

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8
Q

Half-life

A

time it takes for 50% of the drug to be eliminated from the body

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9
Q

Parent compound

A

compound you want to reach the target

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10
Q

Therapeutic index

A
  • lethal dose divided by effective dose
  • takes into account amount of drug (conc.) needed to produce death over the amount of drug needed to produce desired effect
  • higher is better because it means that the drug works super well with an amount very far away from the amount that would cause death
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11
Q

Conformational change

A

change in protein structure, usually due to environmental factors

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12
Q

Direct agonist

A
  • mimics endogenous chemical action
  • activates receptor
  • high affinity
  • high efficacy
  • can be selective or non-selective
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13
Q

Indirect agonist

A
  • enhance endogenous chemical action
  • does not directly affect neurotransmitter or receptor
  • e.g. blocks reuptake or blocks breakdown or alters chemical release
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14
Q

Direct antagonist

A
  • blocks action of receptor (no action)
  • high affinity
  • zero efficacy
  • zero potency
  • selective or non-selective
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15
Q

Indirect antagonist

A
  • reduces endogenous chemical action
  • does not directly affect neurotransmitter or receptor
  • e.g. decrease chemical availability via autoreceptor action
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16
Q

Partial agonist

A
  • binds to the same site as agonist but doesn’t have as much efficacy
  • high affinity
  • low efficacy
17
Q

Partial agonist

A
  • binds to the same site as agonist but doesn’t have as much efficacy (allows only for a certain amount of protein conformation to occur)
  • high affinity
  • low efficacy
18
Q

Allosteric modifiers

A
  • mostly agonists (rarely antagonists)
  • increase efficacy of steric site to make it more likely to bind
  • different binding location than endogenous chemical
  • high affinity
  • high efficacy
19
Q

Inverse agonist

A
  • has negative action/goes below even normal levels (e.g. if channel is normally a little open for ions, inverse agonist makes it so that channel closes a little)
  • prevents change
  • binds at agonist site to prevent binding of agonist
  • decreases functioning of protein itself
  • high affinity
  • high potency
  • binds in a way that lasts longer than antagonist
20
Q

Plasticity

A
  • neurons have emergent properties due to gene by environment interaction
  • this creates stable environments called tonic pools
  • phasic pools are caused by electrical/neurochemical changes in tonic pools
  • –if phasic change is repeated then eventually the tonic pool needs to adapt (e.g. drugs changing brain chemistry)
21
Q

Tonic pools

A
  • tonic pools –> constant and stable environment
  • –develop because some predictable/commonly used pathways are solidified and become energy efficient
  • –common communication between specific neurons = stronger connection
22
Q

Phasic pools

A
  • phasic pools –> formed because of abrupt/anomalous changes in chemical information
  • –allow for cells to respond to errors/injury/signals in order to regain a tonic environment
23
Q

Indirect action

A

alters communication in neighboring cells/environment as opposed to directly changing the biological predisposed physiology

24
Q

Direct action

A
  • drug acts directly on receptor

- ligand binds to receptor’s binding site

25
Q

NMDA and AMPA receptors

A
  • ionotropic
  • NMDA gate Na and Ca (require glutamate or glycine to open)
  • AMPA gate Na and K (ligand gated – glutamate)
  • Mg blocks inside of NMDA and in order for Mg to be removed Na or K must flow through AMPA and depolarize NMDA receptor
  • NMDA receptors regulate number of AMPA receptors at synapse
  • contributes to LTP (strengthening of synapses)
26
Q

Pools

A

pools are dependent on emergent properties and are involved in plasticity