Which side effect profile is most associated with typical antipsychotics compared to atypical antipsychotics?

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Multiple Choice

Which side effect profile is most associated with typical antipsychotics compared to atypical antipsychotics?

Explanation:
Blockade of D2 receptors in different brain pathways underlies the differences here. Typical antipsychotics are strong D2 antagonists, especially in the nigrostriatal pathway, which leads to extrapyramidal symptoms (EPS) and in the tuberoinfundibular pathway, to elevated prolactin levels. Atypical antipsychotics also block D2, but their receptor profile—particularly 5-HT2A antagonism—reduces EPS and prolactin elevation, even though they often bring metabolic side effects like weight gain, dyslipidemia, and glucose intolerance. That combination makes the described pattern the best fit: typicals with higher EPS and hyperprolactinemia, atypicals with lower EPS but greater metabolic risk. Note that some atypicals can still raise prolactin (and some typicals can have metabolic effects), but the overall trend aligns with this option.

Blockade of D2 receptors in different brain pathways underlies the differences here. Typical antipsychotics are strong D2 antagonists, especially in the nigrostriatal pathway, which leads to extrapyramidal symptoms (EPS) and in the tuberoinfundibular pathway, to elevated prolactin levels. Atypical antipsychotics also block D2, but their receptor profile—particularly 5-HT2A antagonism—reduces EPS and prolactin elevation, even though they often bring metabolic side effects like weight gain, dyslipidemia, and glucose intolerance. That combination makes the described pattern the best fit: typicals with higher EPS and hyperprolactinemia, atypicals with lower EPS but greater metabolic risk. Note that some atypicals can still raise prolactin (and some typicals can have metabolic effects), but the overall trend aligns with this option.

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