Navarro V M, Fernández-Fernández R, Nogueiras R, Vigo E, Tovar S, Chartrel N, Le Marec O, Leprince J, Aguilar E, Pinilla L, Dieguez C, Vaudry H, Tena-Sempere M
Department of Cell Biology, Physiology and Immunology, Faculty of Medicine, University of Córdoba, Avda. Menéndez Pidal s/n 14004, Córdoba, Spain.
J Physiol. 2006 May 15;573(Pt 1):237-49. doi: 10.1113/jphysiol.2006.106856. Epub 2006 Mar 16.
The close link between reproductive function and body energy stores relies on a complex neuroendocrine network of common regulatory signals, the nature of which is yet to be fully elucidated. Recently, 26RFa was identified in amphibians and mammals as a conserved hypothalamic neuropeptide of the RFamide family, with a potent orexigenic activity. Yet, despite its proposed role as hypophysiotropic factor, the function of 26RFa in the control of pituitary gonadotropins and, hence, of the reproductive axis remains unexplored. In the present study, the effects of 26RFa on gonadotropin secretion were evaluated in the rat by a combination of in vitro and in vivo approaches. At the pituitary, 26RFa dose-dependently enhanced basal and gonadotropin-releasing hormone (GnRH)-stimulated luteinizing hormone (LH) secretion from male and cyclic female rats. This effect was mimicked by the active fragment 26RFa(20-26), as well as by the related 43RFa peptide. Moreover, expression of the genes encoding 26RFa and its putative receptor, GPR103, was demonstrated in rat pituitary throughout postnatal development. In vivo, intracerebral injection of 26RFa evoked a significant increase in serum LH levels in cyclic and ovariectomized females; this response which was also observed after central injection of 26RFa(20-26) and 43RFa peptides, as well as after systemic administration of 26RFa. Conversely, central and systemic injection of 26RFa failed to significantly modify gonadotropin secretion in adult male rats, even after repeated administration of the peptide. In summary, we present herein novel evidence for the potential role of the orexigenic peptide 26RFa in the control of the gonadotropic axis, thus suggesting its potential involvement in the joint control of energy balance and reproduction, especially in the female.
生殖功能与身体能量储备之间的紧密联系依赖于一个由共同调节信号组成的复杂神经内分泌网络,其本质尚未完全阐明。最近,26RFa在两栖动物和哺乳动物中被鉴定为RFamide家族中一种保守的下丘脑神经肽,具有强大的促食欲活性。然而,尽管它被认为是一种促垂体激素因子,但其在控制垂体促性腺激素以及生殖轴方面的功能仍未被探索。在本研究中,通过体外和体内相结合的方法评估了26RFa对大鼠促性腺激素分泌的影响。在垂体水平,26RFa剂量依赖性地增强了雄性和周期性雌性大鼠基础状态下以及促性腺激素释放激素(GnRH)刺激下的黄体生成素(LH)分泌。活性片段26RFa(20 - 26)以及相关的43RFa肽也能模拟这种效应。此外,在出生后发育过程中,大鼠垂体中编码26RFa及其假定受体GPR103的基因均有表达。在体内,向脑内注射26RFa可使周期性和去卵巢雌性大鼠的血清LH水平显著升高;在向中枢注射26RFa(20 - 26)和43RFa肽以及全身给予26RFa后也观察到了这种反应。相反,即使反复给予该肽,向成年雄性大鼠中枢和全身注射26RFa也未能显著改变促性腺激素的分泌。总之,我们在此提供了新的证据,证明促食欲肽26RFa在控制促性腺轴方面具有潜在作用,从而表明它可能参与能量平衡和生殖的联合调控,尤其是在雌性中。