Watanobe Hajime
Division of Internal Medicine, Clinical Research Center, International University of Health and Welfare, Otawara, Tochigi, Japan.
J Physiol. 2002 Nov 15;545(1):255-68. doi: 10.1113/jphysiol.2002.023895.
It is still not known whether leptin, an adipocyte-derived hormone, acts directly within the hypothalamus to stimulate the gonadotropin-releasing hormone (GnRH)-luteinizing hormone (LH) system. In order to address this question, the present study examined the effects of direct intrahypothalamic perfusions with leptin on the in vivo release of GnRH in ovarian steroid-primed ovariectomized rats utilizing the push-pull perfusion technique. Both alpha-melanocyte-stimulating hormone (alpha-MSH) and neuropeptide Y were also measured in the hypothalamic perfusates. In normally fed animals, the leptin infusion was without effect on the release of these three hypothalamic peptides and also without effect on plasma LH and prolactin (PRL), whether leptin was infused into the medial preoptic area (where the majority of GnRH neuronal cell bodies exist) or the median eminence-arcuate nucleus complex (where axon terminals of GnRH neurons are located). In contrast, in 3-day fasted rats leptin was effective in stimulating the secretion of GnRH, alpha-MSH, and LH, regardless of the site of perfusion. These three hormones were increased in a temporal order of alpha-MSH, GnRH and LH. Irrespective of the site of perfusion, leptin was without effect on the release of neuropeptide Y. Only when leptin was infused into the median eminence-arcuate nucleus complex was PRL secretion also stimulated, although its onset was 1 h behind that of LH. The leptin-induced elevations of GnRH, alpha-MSH, LH and PRL were all dose-dependently stimulated by subnormal (1.0 ng ml(-1)) and normal (3.0 ng ml(-1)) concentrations of leptin, but at higher concentrations (10 ng ml(-1)) it did not produce additional effects. Leptin infusion into the anterior hypothalamic area, a control site equidistant from both the medial preoptic area and the median eminence-arcuate nucleus complex, did not produce a significant change in any of the hormones in either the fed or fasted rats. These results demonstrate for the first time that leptin can act at both the cell bodies and axon terminals of GnRH neurons to stimulate the release of the neurohormone in vivo, and they also suggest that alpha-MSH may play a significant intermediary role in linking leptin and GnRH secretion.
脂肪细胞分泌的激素瘦素是否直接在下丘脑内发挥作用,刺激促性腺激素释放激素(GnRH)-黄体生成素(LH)系统,目前仍不清楚。为了解决这个问题,本研究利用推挽灌注技术,研究了向卵巢类固醇预处理的去卵巢大鼠下丘脑内直接灌注瘦素对GnRH体内释放的影响。同时也检测了下丘脑灌流液中的α-黑素细胞刺激素(α-MSH)和神经肽Y。在正常进食的动物中,无论将瘦素注入内侧视前区(大多数GnRH神经元细胞体所在部位)还是正中隆起-弓状核复合体(GnRH神经元轴突终末所在部位),瘦素输注对这三种下丘脑肽的释放均无影响,对血浆LH和催乳素(PRL)也无影响。相反,在禁食3天的大鼠中,无论灌注部位如何,瘦素均能有效刺激GnRH、α-MSH和LH的分泌。这三种激素按α-MSH、GnRH和LH的时间顺序增加。无论灌注部位如何瘦素对神经肽Y的释放均无影响。只有当瘦素注入正中隆起-弓状核复合体时,PRL分泌才会受到刺激,但其开始时间比LH晚1小时。瘦素诱导的GnRH、α-MSH、LH和PRL升高均受到低于正常浓度(1.0 ng ml⁻¹)和正常浓度(3.0 ng ml⁻¹)的瘦素剂量依赖性刺激,但在较高浓度(10 ng ml⁻¹)时,瘦素没有产生额外的影响。将瘦素注入下丘脑前区(一个与内侧视前区和正中隆起-弓状核复合体距离相等的对照部位),在进食或禁食的大鼠中,任何一种激素均未产生显著变化。这些结果首次证明,瘦素可以作用于GnRH神经元的细胞体和轴突终末,在体内刺激神经激素的释放,并且还表明α-MSH可能在连接瘦素和GnRH分泌方面发挥重要的中介作用。