Adashi E Y, Hsueh A J, Yen S S
Endocrinology. 1981 Apr;108(4):1441-9. doi: 10.1210/endo-108-4-1441.
The role of insulin in the regulation of basal and gonadotropin-releasing hormone (GnRH)-stimulated release of LH and FSH was investigated in vitro using primary cultures of rat anterior pituitary cells from adult ovariectomized rats. Anterior pituitary cells were incubated for 2 days in the presence or absence of insulin in a serum-free medium. At the end of the insulin treatment, the cells were washed and reincubated in the presence or absence of GnRH, and the LH and FSH released into the medium were measured by RIA. Treatment with insulin (1.0 microgram/ml) for 2 days resulted in significant increases in both the basal and the maximal release of LH and FSH, as well as a 3.2- and 6.3-fold decrease in the ED50 values for GnRH in terms of LH and FSH release, respectively. Treatment with increasing concentrations (0.1-10,000 ng/ml) of insulin, led to a dose-dependent increase in the GnRH (3 X 10(-10) M)-stimulated release of both LH and FSH. This effect of insulin was significant (P less than 0.05) at a physiological concentration of 1 ng/ml (24 microU/ml) with an ED50 value of 40 ng/ml. Increasing duration of exposure to insulin resulted in time-dependent increases in the GnRH (3 X 10(-10) M)-stimulated release of LH, becoming significant at 24 h with maximal enhancement observed by 48 h. The effect of insulin was specific; epidermal or fibroblast growth factor did not enhance LH release. The augmenting effect of insulin was not associated with cellular proliferation or an overall change in protein or LH synthesis. Furthermore, the effect of insulin was independent of the ambient glucose concentration. Insulin was, however, without effect on gonadotrophs cultured in a serum-supplemented medium. Our findings suggest that the gonadotroph constitutes a target cell of insulin and that insulin may act directly on the anterior pituitary in the regulation of gonadotropin release.
利用成年去卵巢大鼠的原代垂体前叶细胞进行体外培养,研究胰岛素在调节基础状态以及促性腺激素释放激素(GnRH)刺激下促黄体生成素(LH)和促卵泡生成素(FSH)释放中的作用。垂体前叶细胞在无血清培养基中,于有或无胰岛素的情况下孵育2天。胰岛素处理结束时,将细胞洗涤后,在有或无GnRH的情况下再次孵育,通过放射免疫分析法(RIA)测定释放到培养基中的LH和FSH。用胰岛素(1.0微克/毫升)处理2天导致LH和FSH的基础释放量及最大释放量均显著增加,并且就LH和FSH释放而言,GnRH的半数有效剂量(ED50)值分别降低了3.2倍和6.3倍。用浓度递增(0.1 - 10,000纳克/毫升)的胰岛素处理,导致GnRH(3×10⁻¹⁰摩尔/升)刺激的LH和FSH释放呈剂量依赖性增加。胰岛素在生理浓度1纳克/毫升(24微单位/毫升)时具有显著作用(P<0.05),ED50值为40纳克/毫升。延长胰岛素暴露时间导致GnRH(3×10⁻¹⁰摩尔/升)刺激的LH释放呈时间依赖性增加,在24小时时变得显著,48小时时观察到最大增强效果。胰岛素的作用具有特异性;表皮生长因子或成纤维细胞生长因子不会增强LH释放。胰岛素的增强作用与细胞增殖或蛋白质或LH合成的总体变化无关。此外,胰岛素的作用与环境葡萄糖浓度无关。然而,胰岛素对在补充血清的培养基中培养的促性腺激素细胞没有作用。我们的研究结果表明,促性腺激素细胞是胰岛素的靶细胞,并且胰岛素可能直接作用于垂体前叶以调节促性腺激素的释放。