Helmeste D M, Tang S W
Life Sci. 1983 Dec 19;33(25):2527-33. doi: 10.1016/0024-3205(83)90162-5.
The antidepressants mianserin and amoxapine, and the neuroleptic loxapine caused significant decreases in the number of rat frontal cortex S2-serotonergic receptors after a single acute injection. The affinity of serotonin for this site was also decreased after acute mianserin. Daily injections of loxapine and amoxapine for 2, 7 or 28 days resulted in decreased receptor density but no change in Kd. Down-regulation of S2 sites by mianserin was not dependent on endogenous serotonin stores or occupation of the S2 recognition site since chronic PCPA or acute ketanserin preadministration did not affect the mianserin-induced decreases. The results suggest that mianserin may be acting on other sites which it does not share in common with other S2-antagonists such as ketanserin.
单次急性注射抗抑郁药米安色林和阿莫沙平以及抗精神病药洛沙平后,大鼠额叶皮质S2 - 5-羟色胺能受体数量显著减少。急性注射米安色林后,5-羟色胺对该位点的亲和力也降低。连续2、7或28天注射洛沙平和阿莫沙平导致受体密度降低,但解离常数(Kd)无变化。米安色林对S2位点的下调不依赖于内源性5-羟色胺储备或S2识别位点的占据,因为预先给予慢性对氯苯丙氨酸(PCPA)或急性酮色林并不影响米安色林引起的受体减少。结果表明,米安色林可能作用于其他位点,这些位点与其他S2拮抗剂(如酮色林)并不相同。