Long J B, Youngblood W Y, Kizer J S
Eur J Pharmacol. 1983 Mar 18;88(1):89-97. doi: 10.1016/0014-2999(83)90395-3.
In vivo rates of 5-hydroxytryptophan accumulation (following administration of the decarboxylase inhibitor R04/4602/1) and levels of 5-HT in the nucleus raphe dorsalis (DR), nucleus centralis superior (NCS), nucleus septalis lateralis (LS), nucleus suprachiasmaticus (SCN), nucleus hypothalamicus anterior (AH), and nucleus amygdaloideus centralis (AG) were determined following administration of fluoxetine, 5-methoxy-N,N-dimethyltryptamine, methiothepin, L-tryptophan and reserpine. Fluoxetine and 5-methoxy-N,N-dimethyltryptamine inhibited 5-hydroxytryptophan synthesis in all nuclei, although inhibition of synthesis in the DR was resistant to fluoxetine. Methiothepin inhibited 5-HT synthesis in the DR, NCS, LS and AG, but not in the SCN or AH. L-Tryptophan greatly increased 5HT synthesis in all areas, but this increase was not uniform, being fourfold greater in the NCS than in the LS. Reserpine, while greatly depleting 5HT did not increase 5-hydroxytryptophan synthesis in any nucleus. In no region could changes in brain tryptophan account for the observed drug effects on serotonin metabolism. We conclude that not all CNS serotonergic structures respond to the same drug in a uniform manner.
在给予氟西汀、5-甲氧基-N,N-二甲基色胺、甲硫哒嗪、L-色氨酸和利血平后,测定了体内5-羟色氨酸积累率(在给予脱羧酶抑制剂R04/4602/1之后)以及背侧中缝核(DR)、上中央核(NCS)、外侧隔核(LS)、视交叉上核(SCN)、下丘脑前核(AH)和杏仁中央核(AG)中的5-羟色胺水平。氟西汀和5-甲氧基-N,N-二甲基色胺抑制了所有核团中的5-羟色氨酸合成,尽管DR中合成的抑制对氟西汀有抗性。甲硫哒嗪抑制了DR、NCS、LS和AG中的5-羟色胺合成,但对SCN或AH没有抑制作用。L-色氨酸大大增加了所有区域的5-羟色胺合成,但这种增加并不均匀,NCS中的增加是LS中的四倍。利血平虽然极大地消耗了5-羟色胺,但并未增加任何核团中的5-羟色氨酸合成。在任何区域,脑内色氨酸的变化都无法解释所观察到的药物对5-羟色胺代谢的影响。我们得出结论,并非所有中枢神经系统5-羟色胺能结构对同一种药物的反应都是一致的。