McCann S M, Kimura M, Walczewska A, Karanth S, Rettori V, Yu W H
Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, La., USA.
Neuroimmunomodulation. 1998 May-Aug;5(3-4):193-202. doi: 10.1159/000026337.
Gonadotropin secretion by the pituitary gland is under the control of luteinizing hormone-releasing hormone (LHRH) and the putative follicle-stimulating hormone-releasing factor (FSHRF). Lamprey III LHRH is a potent FSHRF in the rat and appears to be resident in the FSH controlling area of the rat hypothalamus. It is an analog of mammalian LHRH and may be the long-sought FSHRF. Gonadal steroids feedback at hypothalamic and pituitary levels to either inhibit or stimulate the release of LH and FSH, which is also affected by inhibin and activin secreted by the gonads. Important control is exercised by acetylcholine, norepinephrine (NE), dopamine, serotonin, melatonin and glutamic acid (GA). Furthermore, LH and FSH also act at the hypothalamic level to alter secretion of gonadotropins. More recently, growth factors have been shown to have an important role. Many peptides act to inhibit or increase release of LH, and the sign of their action is often reversed by estrogen. A number of cytokines act at the hypothalamic level to suppress acutely the release of LH but not FSH. NE, GA and oxytocin stimulate LHRH release by activation of neural nitric oxide synthase (nNOS). The pathway is as follows: oxytocin and/or GA activate NE neurons in the medial basal hypothalamus (MBH) that activate NOergic neurons by alpha1 receptors. The NO released diffuses into LHRH terminals and induces LHRH release by activation of guanylate cyclase (GC) and cyclooxygenase. NO not only controls release of LHRH bound for the pituitary, but also that which induces mating by actions in the brain stem. An exciting recent development has been the discovery of the adipocyte hormone, leptin, a cytokine related to tumor necrosis factor-alpha (TNF-alpha). In the male rat, leptin exhibits a high potency to stimulate FSH and LH release from hemipituitaries incubated in vitro, and increases the release of LHRH from MBH explants by stimulating the release of NO. LHRH and leptin release LH by activation of NOS in the gonadotropes. The NO released activates GC that releases cyclic GMP which induces LH release. Leptin induces LH release in conscious, ovariectomized estrogen-primed female rats, presumably by stimulating LHRH release. At the effective dose of estrogen to activate LH release, FSH release is inhibited. Leptin may play an important role in induction of puberty and control of LHRH release in the adult as well.
垂体前叶促性腺激素的分泌受促黄体生成素释放激素(LHRH)和假定的促卵泡激素释放因子(FSHRF)的控制。七鳃鳗III型LHRH在大鼠体内是一种有效的FSHRF,似乎存在于大鼠下丘脑的促卵泡激素控制区域。它是哺乳动物LHRH的类似物,可能就是长期寻找的FSHRF。性腺类固醇在下丘脑和垂体水平进行反馈,以抑制或刺激促黄体生成素(LH)和促卵泡激素(FSH)的释放,而这也受到性腺分泌的抑制素和激活素的影响。乙酰胆碱、去甲肾上腺素(NE)、多巴胺、5-羟色胺、褪黑素和谷氨酸(GA)发挥着重要的调控作用。此外,LH和FSH也在下丘脑水平发挥作用,以改变促性腺激素的分泌。最近发现生长因子也发挥着重要作用。许多肽可抑制或增加LH的释放,其作用的正负性常因雌激素而逆转。一些细胞因子在下丘脑水平发挥作用,可急性抑制LH的释放,但不影响FSH的释放。NE、GA和催产素通过激活神经型一氧化氮合酶(nNOS)来刺激LHRH的释放。其途径如下:催产素和/或GA激活下丘脑内侧基底部(MBH)的NE能神经元,这些神经元通过α1受体激活一氧化氮能神经元。释放的一氧化氮扩散到LHRH终末,并通过激活鸟苷酸环化酶(GC)和环氧化酶诱导LHRH的释放。一氧化氮不仅控制着运往垂体的LHRH的释放,还通过在脑干中的作用诱导交配行为。最近一项令人兴奋的进展是发现了脂肪细胞激素瘦素,它是一种与肿瘤坏死因子-α(TNF-α)相关的细胞因子。在雄性大鼠中,瘦素在体外培养的半垂体中具有高效刺激FSH和LH释放的能力,并通过刺激一氧化氮的释放增加MBH外植体中LHRH的释放。LHRH和瘦素通过激活促性腺细胞中的NOS来释放LH。释放的一氧化氮激活GC,后者释放环磷酸鸟苷,从而诱导LH的释放。瘦素在有意识的、切除卵巢并用雌激素预处理的雌性大鼠中诱导LH的释放,可能是通过刺激LHRH的释放来实现的。在激活LH释放的有效雌激素剂量下,FSH的释放受到抑制。瘦素在青春期的启动以及成年期LHRH释放的控制中可能也发挥着重要作用。