Igarashi M
Department of Obstetrics and Gynecology, Gunma University School of Medicine, Maebashi.
Nihon Sanka Fujinka Gakkai Zasshi. 1988 Aug;40(8):973-8.
FSH secretion from the pituitary is now generally believed to be controlled only by LH-RH. However, since 1971 I have been publishing lines of evidence suggesting that FSH is controlled by both LH-RH and FSH-RH distinct from LH-RH. Recent accumulated reports suggest that lots of data cannot be explained by the one-RH theory. The one-RH theory means that both LH and FSH are regulated by a sole releasing factor, LH-RH. In 1985 we succeeded in purification of porcine and bovine follicular inhibin for the first time in the world. Its molecular weight was 32,000, which consisted of alpha-subunit (mw 20,000) and beta-subunit (mw 13,000). The site of production of inhibin was confirmed to be granulosa cell by immuno-histochemical technique and to be corpus luteum by RIA. Secretion of inhibin was stimulated by FSH, insulin, platelet extract, dibutyryl c-AMP, cholera toxin, forskolin, and inhibited by cortisol. Testosterone augmented FSH action. In the pituitary cells, inhibin inhibited synthesis of FSH, so cycloheximide could mimicked inhibin action in vitro. Inhibin did not inhibit LH release from the pituitary, but LH release stimulated by LH-RH was also inhibited by inhibin in vitro. Using anti-porcine inhibin antibody and anti bovine inhibin antibody prepared by us, we could measure blood inhibin levels during rat, pig, cow and goat sexual cycles, human menstrual cycle, human pregnancy, and clomiphene-HMG stimulated menstrual cycle. We found maximum blood inhibin levels in the luteal phase and during pregnancy. These high levels of inhibin were demonstrated to be derived from the corpus luteum, pregnant corpus luteum and placenta.(ABSTRACT TRUNCATED AT 250 WORDS)
目前普遍认为,垂体分泌促卵泡激素(FSH)仅受促黄体生成素释放激素(LH-RH)的控制。然而,自1971年以来,我陆续发表了一系列证据,表明FSH受LH-RH和与LH-RH不同的促卵泡激素释放激素(FSH-RH)的共同控制。最近积累的报告表明,许多数据无法用单一释放激素理论来解释。单一释放激素理论是指LH和FSH均由单一的释放因子LH-RH调节。1985年,我们首次在世界上成功纯化了猪和牛的卵泡抑制素。其分子量为32,000,由α亚基(分子量20,000)和β亚基(分子量13,000)组成。通过免疫组织化学技术证实抑制素的产生部位是颗粒细胞,通过放射免疫分析(RIA)证实是黄体。促卵泡激素、胰岛素、血小板提取物、二丁酰环磷腺苷(c-AMP)、霍乱毒素、福斯高林可刺激抑制素的分泌,而皮质醇则抑制其分泌。睾酮增强FSH的作用。在垂体细胞中,抑制素抑制FSH的合成,因此在体外环己酰亚胺可模拟抑制素的作用。抑制素不抑制垂体释放LH,但在体外,LH-RH刺激的LH释放也受抑制素抑制。使用我们制备的抗猪抑制素抗体和抗牛抑制素抗体,我们能够测定大鼠、猪、牛和山羊性周期、人类月经周期、人类妊娠以及克罗米芬-人绝经期促性腺激素(HMG)刺激的月经周期中的血液抑制素水平。我们发现黄体期和妊娠期血液抑制素水平最高。这些高水平的抑制素被证明来自黄体、妊娠黄体和胎盘。(摘要截取自250词)