Psychopharmacology Flashcards

(16 cards)

1
Q

Differentiate asymmetric and symmetric synapses.

A

Asymmetric: Excitatory; features a prominent postsynaptic density.
Symmetric: Inhibitory; features a less prominent postsynaptic density.

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2
Q

What is an ionotropic receptor?

A
  • Ligand-gated ion channels
  • Fast, direct effects on membrane potential
  • Cause immediate depolarisation or hyperpolarisation
  • E.g., AMPA, NMDA (glutamate); GABA-A
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3
Q

What is a metabotropic receptor?

A
  • G-protein-coupled receptors (GPCRs)
  • Indirect, slower effects via second messengers
  • Modulate gene expression, plasticity, excitability
  • E.g., GABA-B, dopamine D1–D5, muscarinic ACh
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4
Q

What are the three subunits of G-proteins?

A

Alpha (α), Beta (β), and Gamma (γ) subunits.

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5
Q

What do Gs-coupled receptors do?

A
  • Activate adenylyl cyclase → ↑ cAMP
  • Enhances plasticity, gene expression, and excitability
  • Promotes depolarisation
  • Example: Dopamine D1 receptors
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6
Q

What do Gi-coupled receptors do?

A
  • Inhibit adenylyl cyclase → ↓ cAMP
  • Open K⁺ channels → hyperpolarisation
  • Reduces plasticity and neuronal firing
  • Example: Dopamine D2 receptors
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7
Q

What are the main types of glutamate receptors and their functions?

A

AMPA (ionotropic):
* Opens with glutamate binding
* Allows Na⁺ influx → fast EPSPs
NMDA (ionotropic):
* Requires glutamate, glycine, and depolarisation to remove Mg²⁺ block
* Allows Na⁺ and Ca²⁺ influx → promotes plasticity and learning
* Highly gated to prevent excitotoxicity
mGlu (metabotropic):
* Activates G-proteins
* Increases plasticity and excitability

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8
Q

What are the main types of GABA receptors and their functions?

A

GABA-A (ionotropic):
* Opens Cl⁻ channels → hyperpolarisation
* Fast inhibitory effect
GABA-B (metabotropic):
* Activates K⁺ channels via G-proteins
* Slower, prolonged inhibition

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9
Q

How do agonists affect neurotransmitter systems?

A

Enhance neurotransmitter action
* Mimic neurotransmitters (e.g., L-DOPA, MDMA)
* Block reuptake (e.g., SSRIs, cocaine)
* Inhibit degradation (e.g., MAOIs)

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10
Q

How do antagonists affect neurotransmitter systems?

A

Block neurotransmitter action
* Bind receptors without activating them
* E.g., naloxone (opioid), ketamine (NMDA), antipsychotics (D2), propranolol (β-adrenergic)

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11
Q

How does ketamine act on NMDA receptors?

A
  • NMDA antagonist
  • Blocks the channel (mimics Mg²⁺ plug) even when glutamate and glycine are bound
  • Preferentially targets NMDA receptors on inhibitory interneurons → increased excitation at low doses
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12
Q

What is D-cycloserine (DCS) and how does it affect NMDA receptors?

A
  • Partial agonist at the glycine site of NMDA receptors
  • Enhances likelihood of receptor opening
  • Promotes plasticity and learning
  • Used experimentally to enhance extinction learning
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13
Q

How do benzodiazepines affect GABA-A receptors?

A
  • Positive allosteric modulators
  • Bind to specific α subunits
  • Enhance GABA’s inhibitory effect by increasing Cl⁻ influx
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14
Q

How do hypnotics (e.g., barbiturates) affect GABA-A receptors?

A
  • Positive allosteric modulators.
  • Bind to α1 subunits of GABA-A receptors
  • Enhance duration of Cl⁻ influx → hyperpolarisation
  • Induces enhanced and prolonged inhibition
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15
Q

What is optogenetics and how does it work?

A
  • Uses light-activated ion channels
  • Light triggers immediate activation or inhibition of targeted neurons
  • Enables precise control of neural activity during behaviour
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16
Q

What is chemogenetics and how does it work?

A
  • Uses engineered GPCRs (DREADDs) activated by synthetic ligand (CNO)
  • Modulates neuronal excitability via second messengers
  • Allows selective, reversible control of specific neural circuits