Smythe G A, Brandstater J F, Lazarus L
Neuroendocrinology. 1975;17(3):245-57. doi: 10.1159/000122360.
The ability of 5-hydroxyl-L-tryptophan (5-HTP) or pentobarbital anesthesia to elevate rat serum GH levels is completely blocked by the simultaneous administration of the serotonin antagonist cyprophepatidine, as well as by the pineal gland principles melatonin and 5-methoxytryptamine (5-MT), and by the 0-methylated dopamine derivative 3,4-dimethoxyphenylethylamine (DMPEA). Small doses of 5-MT cause paradoxical elevations in serum rat GH but at the same time inhibit the action of 5-HTP. Blockade of dopaminergic pathways by treatment with either DMPEA or chlorpromazine causes a slight, nonsignificant suppression of serum GH in normal rats while serum prolactin levels are increased greater than tenfold showing that, unlike prolactin, rat GH is not subject to tonic inhibitory control by dopamine. The data presented support the recently advanced hypothesis that rat GH is under serotoninergic CONTROL AND DEMONSTRATE THAT GH secretion can be significantly suppressed by serotoninergic blockade. It is suggested that the results presented here for monoamine control of rat GH release are not a variance with those reported for man.
5-羟基-L-色氨酸(5-HTP)或戊巴比妥麻醉提高大鼠血清生长激素(GH)水平的能力,会被同时给予血清素拮抗剂赛庚啶、松果体物质褪黑素和5-甲氧基色胺(5-MT)以及0-甲基化多巴胺衍生物3,4-二甲氧基苯乙胺(DMPEA)完全阻断。小剂量的5-MT会使大鼠血清GH出现反常升高,但同时会抑制5-HTP的作用。用DMPEA或氯丙嗪处理阻断多巴胺能途径,会使正常大鼠的血清GH略有抑制但无显著意义,而血清催乳素水平则升高超过十倍,这表明与催乳素不同,大鼠GH不受多巴胺的紧张性抑制控制。所呈现的数据支持了最近提出的假说——大鼠GH受血清素能控制,并证明血清素能阻断可显著抑制GH分泌。有人认为,这里给出的关于单胺对大鼠GH释放控制的结果与人类报道的结果并无差异。