Vlasses P H, Rotmensch H H, Swanson B N, Clementi R A, Ferguson R K
Department of Medicine, Jefferson Medical College of Thomas Jefferson University, Philadelphia, PA 19107.
J Endocrinol Invest. 1989 Feb;12(2):87-91. doi: 10.1007/BF03349926.
To evaluate changes in serum prolactin and plasma and urine aldosterone after a serotonergic challenge, 8 healthy men (19 to 42 yr), taking dexamethasone (0.75 mg qid), received the serotonin precursor L-5-hydroxytryptophan (L5HTP; 100 mg qid) with the peripheral decarboxylase inhibitor carbidopa (C; 50 mq qid) or matching placebos in a randomized, crossover manner. Serum prolactin concentration increased in all subjects after L5HTP/C in comparison to placebo, mean (SD) prolactin (ng/ml) at 8 h after dosing was 19.8 +/- 6.3 after L5HTP/C and 12.0 +/- 3.1 after placebo (p less than 0.05). In contrast, in comparison to values on placebo, L5HTP/C had no apparent effect on mean plasma concentration at all observation times; mean (SD) aldosterone (ng/dl) at 8 h after dosing was 12.0 +/- 5.1 and 12.0 +/- 3.8 after placebo (NS). Mean (SD) urinary aldosterone (micrograms/24 h), Na+(mEq/24 h) and K+(mEq/24 h) excretion were 7.0 +/- 4.4, 49.3 +/- 30.6, 30.1 +/- 11.2, after L5HTP/C and 7.4 +/- 5.8, 59.7 +/- 23.9, 33.3 +/- 7.4 after placebo (NS). Under these study conditions, subacute serotonergic stimulation with oral L5HTP/C resulted in prolactin but not aldosterone release.
为评估血清素激发后血清催乳素、血浆和尿醛固酮的变化,8名健康男性(19至42岁),正在服用地塞米松(每日4次,每次0.75毫克),以随机、交叉方式接受血清素前体L - 5 - 羟色氨酸(L5HTP;每日4次,每次100毫克)与外周脱羧酶抑制剂卡比多巴(C;每日4次,每次50毫克)或匹配的安慰剂。与安慰剂相比,所有受试者在服用L5HTP/C后血清催乳素浓度均升高,给药后8小时催乳素的平均(标准差)浓度(纳克/毫升)在服用L5HTP/C后为19.8±6.3,服用安慰剂后为12.0±3.1(p<0.05)。相比之下,与安慰剂的值相比,L5HTP/C在所有观察时间对平均血浆浓度均无明显影响;给药后8小时醛固酮的平均(标准差)浓度(纳克/分升)在服用安慰剂后为12.0±5.1和12.0±3.8(无显著性差异)。服用L5HTP/C后尿醛固酮的平均(标准差)排泄量(微克/24小时)、钠(毫当量/24小时)和钾(毫当量/24小时)分别为7.0±4.4、49.3±30.6、30.1±11.2,服用安慰剂后分别为7.4±5.8、59.7±23.9、33.3±7.4(无显著性差异)。在这些研究条件下,口服L5HTP/C进行亚急性血清素刺激可导致催乳素释放,但不会导致醛固酮释放。