Psychopharmacology Flashcards
What are the monoamine NT systems?
Noradrenaline, dopamine, serotonin
adrenaline + histamine are also monoamines
What are the two main groups of symptoms in psychiatric disorders?
Affective (anxiety + depression)
Psychotic (bipolar / schizophrenia)
Which NTs involved in depression, schizophrenia and ADHD?
depression: NA, 5HT
schizophrenia: DA, 5HT
ADHD: NA, DA
Why are monoaminergic neurons different to glutamatergic neurons?
Monoamine neurons: cell bodies sit in groups of nuclei which project to different parts of brain.
Great diversity of post-synaptic receptors: results in diversity of function that transmitter known to modulate
e.g. NA neuron, 90% neurons found in locus coeruleus at back of brainstem, then sends projections to frontal regions
What is monamine oxidase + COMT?
Monoamine oxidase + Catechol-O-methyltransferase (COMT) = intracellular enzymes, inactivate/degrade monoamines?
Where are monoamine reuptake transporters located?
Both the dendritic/cell body region & terminal region
Also on glial cells
How do autoreceptors produce negative feedback in monoaminergic neurons?
Inhibitory effect on calcium channels + positive effect on K+ channels → hyperpolarisation → reduced excitability of nerve (more depolarisation needed to elicit exocytosis)
How do autoreceptors produce negative feedback in monoaminergic neurons?
Inhibitory effect on calcium channels + positive effect on K+ channels → hyperpolarisation → reduced excitability of nerve (more depolarisation needed to elicit exocytosis)
e.g. a2 adrenoreceptor: Gi coupling (reduces cAMP, inactivates calcium channels, activates potassium channels)
How do serotonin and noradrenaline neurons interact?
NA= major regulator of the serotonin system: projections from locus coeruleus → dorsal raphe (synapse onto cell bodies in dorsal raphe)
Reciprocal: feedback from serotonergic system to LC via an interneuron
NA input to DR acts on a1 receptors (GPCR) stimulate firing (therefore calcium-dependent serotonin release)
Or if NA is released onto terminal region at synapse can inhibit 5-HT release through activation of alpha2-autoreceptors