Dubey A K, Zeleznik A J, Plant T M
Department of Physiology, University of Pittsburgh School of Medicine, Pennsylvania 15261.
Endocrinology. 1987 Dec;121(6):2229-37. doi: 10.1210/endo-121-6-2229.
In the male rhesus monkey, the negative feedback regulation of gonadotropin secretion by the gonad appears to involve a specific inhibitory action of testicular hormone on FSH release at the level of the anterior pituitary gland. The purpose of the present study, which used the hypophysiotropic clamp preparation, was to determine whether circulating testosterone (T) or estradiol (E) comprises a major component of the testicular FSH-inhibiting factor in this species. Endogenous hypothalamic GnRH secretion was abolished or severely compromised in five adult male rhesus monkeys by placement of radiofrequency lesions in the region of the arcuate nucleus. Subsequently, an episodic pattern of activity in the pituitary-Leydig cell axis of these animals was restored by a chronic and unchanging intermittent iv infusion of GnRH (0.1 microgram/min for 3 min ever 3 h), which appears to provide the gonadotropes of lesioned animals with a hypophysiotropic drive comparable to that produced by the hypothalamus of animals with an intact central nervous system. Treatment of three animals with a specific anti-E-gamma-globulin fraction resulted in a marked and sustained rise in E-binding activity in serum, but this neutralization of circulating E did not elicit hypersecretion of FSH. In all five animals, initiation of T replacement on the day of orchidectomy, which maintained circulating T concentrations in the high testis-intact control range, failed to prevent the postcastration hypersecretion of FSH that is evoked after removal of testis in the hypophysiotropic clamp preparation. As expected, the changes in circulating LH levels during immunoneutralization and after orchidectomy and T replacement were unremarkable. These findings indicate that neither circulating T nor E can account for the testicular inhibition of FSH secretion in the rhesus monkey and thus lead, by a process of exclusion, to the view that in this species the negative feedback regulation of FSH release by the testis is mediated directly at the level of the gonadotrope by an inhibitory action of a nonsteroidal hormone, most probably the recently identified gonadal peptide inhibin.
在雄性恒河猴中,性腺对促性腺激素分泌的负反馈调节似乎涉及睾丸激素对垂体前叶促卵泡激素(FSH)释放的特异性抑制作用。本研究采用垂体促性腺激素钳夹制备法,目的是确定循环睾酮(T)或雌二醇(E)是否构成该物种睾丸FSH抑制因子的主要成分。通过在弓状核区域放置射频损伤,消除或严重损害了五只成年雄性恒河猴内源性下丘脑促性腺激素释放激素(GnRH)的分泌。随后,通过慢性且不变的间歇性静脉输注GnRH(每3小时0.1微克/分钟,持续3分钟)恢复了这些动物垂体-莱迪希细胞轴的周期性活动模式,这似乎为受损动物的促性腺激素细胞提供了与具有完整中枢神经系统动物的下丘脑产生的促垂体驱动相当的促垂体驱动。用特异性抗E-γ球蛋白组分治疗三只动物导致血清中E结合活性显著且持续升高,但循环E的这种中和并未引发FSH的分泌过多。在所有五只动物中,在睾丸切除当天开始进行T替代,使循环T浓度维持在高睾丸完整对照范围内,但未能预防垂体促性腺激素钳夹制备法中睾丸切除后诱发的去势后FSH分泌过多。正如预期的那样,免疫中和期间以及睾丸切除和T替代后循环促黄体生成素(LH)水平的变化不明显。这些发现表明,循环T和E均不能解释恒河猴睾丸对FSH分泌的抑制作用,因此通过排除过程得出这样的观点,即在该物种中,睾丸对FSH释放的负反馈调节是由一种非甾体激素的抑制作用直接在促性腺激素细胞水平介导的,很可能是最近发现的性腺肽抑制素。