Lindström P, Ohlsson L
Endocrinology. 1987 Feb;120(2):780-4. doi: 10.1210/endo-120-2-780.
The importance of monoaminergic mechanisms for the regulation of GH-releasing factor (GRF)-stimulated GH secretion was studied in perifused rat anterior pituitaries. Dopamine (greater than 1 microL) reduced GRF-stimulated GH release, but 5-hydroxytryptamine (5-HT; 1 mL) had no effect. The substrates for L-aromatic amino acid decarboxylase, L-5-hydroxy-tryptophan(L-5-HTP; 10 microM) L-dihydroxyphenylalanine; (1 mM), D,L-o-tyrosine (2 mM), and D,L-m-tyrosine (2 mM), all reduced GRF-stimulated GH release. Inhibition of the L-aromatic amino acid decarboxylase by benserazide (0.1 mM), carbidopa (0.1 mM), or alpha-monofluoromethyldopa (0.1 mM) did not reduce the effect of the decarboxylase substrates on GH secretion. The enzyme inhibitors had no influence on hormone secretion per se. The findings indicate that dopamine may inhibit GRF-induced GH release at the pituitary level and that the precursor amino acids inhibit GH secretion independently of the formation of the corresponding amines.
在灌流的大鼠垂体前叶中研究了单胺能机制对生长激素释放因子(GRF)刺激的生长激素分泌调节的重要性。多巴胺(大于1微升)减少了GRF刺激的生长激素释放,但5-羟色胺(5-HT;1毫升)没有作用。L-芳香族氨基酸脱羧酶的底物,L-5-羟色氨酸(L-5-HTP;10微摩尔)、L-二羟基苯丙氨酸(1毫摩尔)、D,L-邻酪氨酸(2毫摩尔)和D,L-间酪氨酸(2毫摩尔),均减少了GRF刺激的生长激素释放。苄丝肼(0.1毫摩尔)、卡比多巴(0.1毫摩尔)或α-单氟甲基多巴(0.1毫摩尔)对L-芳香族氨基酸脱羧酶的抑制并未降低脱羧酶底物对生长激素分泌的作用。这些酶抑制剂本身对激素分泌没有影响。研究结果表明,多巴胺可能在垂体水平抑制GRF诱导的生长激素释放,并且前体氨基酸独立于相应胺的形成抑制生长激素分泌。