Psychopharmacology Flashcards
(16 cards)
Differentiate asymmetric and symmetric synapses.
Asymmetric: Excitatory; features a prominent postsynaptic density.
Symmetric: Inhibitory; features a less prominent postsynaptic density.
What is an ionotropic receptor?
- Ligand-gated ion channels
- Fast, direct effects on membrane potential
- Cause immediate depolarisation or hyperpolarisation
- E.g., AMPA, NMDA (glutamate); GABA-A
What is a metabotropic receptor?
- 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
What are the three subunits of G-proteins?
Alpha (α), Beta (β), and Gamma (γ) subunits.
What do Gs-coupled receptors do?
- Activate adenylyl cyclase → ↑ cAMP
- Enhances plasticity, gene expression, and excitability
- Promotes depolarisation
- Example: Dopamine D1 receptors
What do Gi-coupled receptors do?
- Inhibit adenylyl cyclase → ↓ cAMP
- Open K⁺ channels → hyperpolarisation
- Reduces plasticity and neuronal firing
- Example: Dopamine D2 receptors
What are the main types of glutamate receptors and their functions?
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
What are the main types of GABA receptors and their functions?
GABA-A (ionotropic):
* Opens Cl⁻ channels → hyperpolarisation
* Fast inhibitory effect
GABA-B (metabotropic):
* Activates K⁺ channels via G-proteins
* Slower, prolonged inhibition
How do agonists affect neurotransmitter systems?
Enhance neurotransmitter action
* Mimic neurotransmitters (e.g., L-DOPA, MDMA)
* Block reuptake (e.g., SSRIs, cocaine)
* Inhibit degradation (e.g., MAOIs)
How do antagonists affect neurotransmitter systems?
Block neurotransmitter action
* Bind receptors without activating them
* E.g., naloxone (opioid), ketamine (NMDA), antipsychotics (D2), propranolol (β-adrenergic)
How does ketamine act on NMDA receptors?
- 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
What is D-cycloserine (DCS) and how does it affect NMDA receptors?
- Partial agonist at the glycine site of NMDA receptors
- Enhances likelihood of receptor opening
- Promotes plasticity and learning
- Used experimentally to enhance extinction learning
How do benzodiazepines affect GABA-A receptors?
- Positive allosteric modulators
- Bind to specific α subunits
- Enhance GABA’s inhibitory effect by increasing Cl⁻ influx
How do hypnotics (e.g., barbiturates) affect GABA-A receptors?
- Positive allosteric modulators.
- Bind to α1 subunits of GABA-A receptors
- Enhance duration of Cl⁻ influx → hyperpolarisation
- Induces enhanced and prolonged inhibition
What is optogenetics and how does it work?
- Uses light-activated ion channels
- Light triggers immediate activation or inhibition of targeted neurons
- Enables precise control of neural activity during behaviour
What is chemogenetics and how does it work?
- Uses engineered GPCRs (DREADDs) activated by synthetic ligand (CNO)
- Modulates neuronal excitability via second messengers
- Allows selective, reversible control of specific neural circuits