Lancranjan I, Wirz-Justice A, Pühringer W, Del Pozo E
J Clin Endocrinol Metab. 1977 Sep;45(3):588-93. doi: 10.1210/jcem-45-3-588.
The effect of a new soluble ester of 1-5 hydroxytryptophan (1-5 HTP, Ro 3-5940, 200 mg infusion) on prolactin (PRL) and growth hormone (GH) release was tested in 11 young, healthy subjects (6 men, 5 women). To minimize side-effects, peripheral decarboxylase inhibition was achieved with benserazide (Ro 4-4602.) PRL increased significantly (P less than 0.01) after benserazide alone in all subjects. A further significant increase (P less than 0.01) of PRL plasma levels occurred only in women up to 90 min after the infusion of 1-5 HTP was discontinued. Benserazide administration had no effect of basal GH levels, but a significant increase of GH release (P less than 0.01) was noticed 30-120 min after the end of 1-5 HTP infusion in both men and women. The mean peak value of GH plasma levels after 1-5 HTP administration was 32.0 +/- 8.8 ng/ml. It was postulated that benserazide penetrated at the level of the pituitary, decreasing the synthesis of dopamine and consequently reducing its known inhibitory effect on PRL release. The PRL increase (statistically significant only in women), as well as the release of GH after 1-5 HTP infusion, was considered as further evidence for stimulatory serotoninergic control of both PRL and GH secretion.
在11名年轻健康受试者(6名男性,5名女性)中测试了一种新型1-5羟色氨酸可溶性酯(1-5 HTP,Ro 3-5940,200毫克静脉输注)对催乳素(PRL)和生长激素(GH)释放的影响。为了尽量减少副作用,使用苄丝肼(Ro 4-4602)实现外周脱羧酶抑制。单独使用苄丝肼后,所有受试者的PRL均显著升高(P<0.01)。仅在停止输注1-5 HTP后长达90分钟的女性中,PRL血浆水平进一步显著升高(P<0.01)。苄丝肼给药对基础GH水平无影响,但在1-5 HTP输注结束后30-120分钟,男性和女性的GH释放均显著增加(P<0.01)。1-5 HTP给药后GH血浆水平的平均峰值为32.0±8.8 ng/ml。据推测,苄丝肼在垂体水平穿透,减少多巴胺的合成,从而降低其对PRL释放已知的抑制作用。PRL的升高(仅在女性中具有统计学意义)以及1-5 HTP输注后GH的释放,被视为PRL和GH分泌受5-羟色胺能刺激控制的进一步证据。