Ugriumov M V, Taxi J, Steinbusch H W, Tramu G
Zh Evol Biokhim Fiziol. 1989 May-Jun;25(3):324-9.
An attempt has been made to reveal 5-HT immunopositive (IP) neurones in the hypothalamus of intact foetuses (18th day of gestation) and neonatal (9-day) rats under normal conditions and after their treatment with drugs involved into 5-HT metabolism or into regulation of its uptake by serotoninergic neurones. 5-HTIP cells were not observed in intact animals as well as after L-tryptophan treatment, whereas two large colonies of these neurones were found in the anterio-lateral hypothalamus and dorsomedial nucleus after subsequent injections of monoamine oxidase inhibitor, pargyline, and amino acid precursor of 5-HT synthesis, L-tryptophan. Significantly less intensive reaction was observed after injections of another precursor of 5-HT synthesis, 5-hydroxytryptophan, or pargyline only. Immunostaining evoked by pargyline or L-tryptophan can be prevented by preliminary injections of fluoxetine, a specific inhibitor of 5-HT uptake by serotoninergic neurones. These data suggest that the immunostaining of hypothalamic neurones is due to their capacity to take up specifically 5-HT from the environment rather than to its intraneuronal synthesis from L-tryptophan. However, 5-HT synthesis from 5-hydroxytryptophan in the same cells may also take place. The uptake of extracellular 5-HT by catecholaminergic neurones is absent, since nomifensine, a specific inhibitor of this uptake, does not affect immunostaining.
研究人员试图揭示在正常条件下以及用参与5-羟色胺(5-HT)代谢或调节其被5-羟色胺能神经元摄取的药物处理后,完整胎儿(妊娠第18天)和新生(9日龄)大鼠下丘脑内的5-HT免疫阳性(IP)神经元。在完整动物以及L-色氨酸处理后均未观察到5-HTIP细胞,而在随后注射单胺氧化酶抑制剂优降宁和5-HT合成的氨基酸前体L-色氨酸后,在丘脑前外侧和背内侧核中发现了两群此类神经元。仅注射5-HT合成的另一种前体5-羟色氨酸或优降宁后,观察到的反应强度明显较低。优降宁或L-色氨酸引起的免疫染色可通过预先注射氟西汀(一种5-羟色胺能神经元摄取5-HT的特异性抑制剂)来预防。这些数据表明,下丘脑神经元的免疫染色是由于它们从环境中特异性摄取5-HT的能力,而不是由于其从L-色氨酸进行的神经元内合成。然而,同一细胞中也可能发生从5-羟色氨酸合成5-HT的过程。由于诺米芬辛(这种摄取的特异性抑制剂)不影响免疫染色,所以儿茶酚胺能神经元不存在摄取细胞外5-HT的情况。