Dubey A K, Cameron J L, Steiner R A, Plant T M
Endocrinology. 1986 Feb;118(2):518-25. doi: 10.1210/endo-118-2-518.
The purpose of this study was to examine further the notion that in higher primates, analogous neuroendocrine mechanisms may underlie the hiatus in LH and FSH secretion during prepubertal development and the suppression of gonadotropin release in adults during states of malnutrition. To this end, the metabolic sequelae and the gonadotropin response to restricted food intake (RFI) were determined in nine castrated male rhesus monkeys. The results obtained were then evaluated in light of current understanding of the neuroendocrine bases of the ontogeny of gonadotropin secretion in primates. A reduction in food intake from approximately 1150 Cal/day to approximately 200 Cal/day for 20-34 days resulted in declines in body weight and circulating LH and FSH concentrations. The reduction in body weight and the suppression of LH secretion were statistically significant (P less than 0.05). The decrease in gonadotropin secretion induced by RFI was fully restored by the chronic iv intermittent infusion of GnRH (0.1 microgram/min for 3 min every hour). These findings graphically demonstrate that RFI, or a sequelae of this nutritional perturbation, inhibits gonadotropin secretion, in the absence of feedback influences by gonadal hormones, by an action at a suprapituitary level that is mediated by interruption of intermittent hypothalamic GnRH discharge. The apparent arrest of the neural mechanism that governs the timing of intermittent GnRH discharge, the so-called GnRH pulse generator, was associated with decreases in plasma insulin (P = 0.078), T4 (P less than 0.05), and T3 (P less than 0.05) concentrations and with a significant (P less than 0.05) elevation in circulating cortisol levels. Although a general decrease in circulating amino acid levels was not observed during RFI, plasma glutamate concentrations were significantly (P less than 0.05) reduced by the nutritional perturbation. RFI resulted in unremarkable hypoglycemia. While the suppression of gonadotropin secretion in castrated male monkeys during RFI resembled, in certain aspects, the hiatus in gonadotropin secretion during prepubertal development, the endocrine and metabolic concomitants of these two physiological states exhibited important differences. Thus, the contemporary notion that the study of dietary restriction in adult primates may provide insights into the neuroendocrine mechanisms that govern the timing of the onset of puberty in these species should not be accepted without careful consideration.
在高等灵长类动物中,类似的神经内分泌机制可能是青春期前发育过程中促黄体生成素(LH)和促卵泡生成素(FSH)分泌中断以及成年期营养不良状态下促性腺激素释放受抑制的基础。为此,我们测定了9只去势雄性恒河猴在食物摄入量受限(RFI)情况下的代谢后遗症以及促性腺激素反应。然后,根据目前对灵长类动物促性腺激素分泌个体发生的神经内分泌基础的理解,对所得结果进行评估。食物摄入量从约1150卡路里/天减少到约200卡路里/天,持续20 - 34天,导致体重、循环中的LH和FSH浓度下降。体重减轻和LH分泌受抑制具有统计学意义(P < 0.05)。通过慢性静脉内间歇性输注促性腺激素释放激素(GnRH,每小时0.1微克/分钟,持续3分钟),RFI诱导的促性腺激素分泌减少完全恢复。这些发现清楚地表明,RFI或这种营养紊乱的后遗症,在不存在性腺激素反馈影响的情况下,通过作用于垂体上水平(由下丘脑GnRH间歇性释放中断介导)来抑制促性腺激素分泌。控制间歇性GnRH释放时间的神经机制,即所谓的GnRH脉冲发生器,明显停止,这与血浆胰岛素(P = 0.078)、甲状腺素(T4,P < 0.05)和三碘甲状腺原氨酸(T3,P < 0.05)浓度降低以及循环皮质醇水平显著升高(P < 0.05)有关。尽管在RFI期间未观察到循环氨基酸水平普遍下降,但营养紊乱使血浆谷氨酸浓度显著降低(P < 0.05)。RFI导致不明显的低血糖。虽然去势雄性猴子在RFI期间促性腺激素分泌受抑制在某些方面类似于青春期前发育过程中促性腺激素分泌的中断,但这两种生理状态的内分泌和代谢伴随情况存在重要差异。因此,关于研究成年灵长类动物饮食限制可能为控制这些物种青春期开始时间的神经内分泌机制提供见解的当代观点,在未经仔细考虑的情况下不应被接受。