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Psychiatry · Psychotic disorders: antipsychotic potency and receptor
Sample itemWhen the daily clinical doses of conventional antipsychotics are compared with their binding properties, the dose needed correlates most closely with the affinity of the drug for which receptor?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Dopamine D2 receptor
The clinical potency of conventional antipsychotics tracks their D2 receptor affinity, which was a major support for the dopamine hypothesis. Effects at muscarinic, histaminic and adrenergic receptors explain side effects such as dry mouth, sedation and hypotension instead.
Option by option
A. Muscarinic M1 receptor
M1 blockade explains anticholinergic side effects, not antipsychotic potency.
B. Alpha-1 adrenergic receptor
Alpha-1 blockade explains orthostatic hypotension, not antipsychotic potency.
C. Dopamine D2 receptor (correct)
Correct. Potency parallels D2 binding affinity, supporting the dopamine hypothesis.
D. Histamine H1 receptor
H1 blockade explains sedation and weight gain, not antipsychotic potency.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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