Role of neuropeptides and amino acids in controlling secretion of hormones from the anterior pituitary gland in pigs.

M. Estienne, J. Harter-Dennis, C. Barb
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引用次数: 18

Abstract

All reproductive processes involve one or more of the protein hormones secreted from the anterior pituitary gland: LH, FSH, prolactin, growth hormone, ACTH and thyroid-stimulating hormone (TSH). Primary hormones of reproduction, such as LH and FSH, directly regulate a reproductive activity. For example, LH and FSH stimulate follicular growth and the associated secretion of oestradiol in sows. In contrast, secondary hormones of reproduction such as TSH are permissive and regulate other physiological systems that indirectly, but profoundly, influence reproduction. Reproduction in pigs can be enhanced by developing strategies to alter and control secretion of hormones from the anterior pituitary gland. However, the successful manipulation of adenohypophysial hormone secretion will require a sound understanding of the mechanisms controlling the function of the hypothalamic-pituitary axis. Hypothalamic hormones including GnRH, dopamine, growth hormone-releasing hormone (GHRH), somatostatin, corticotrophin-releasing hormone (CRH) and thyrotrophin-releasing hormone (TRH) are synthesized in perikarya that possess axons that terminate at the median eminence. These hormones are released into the hypothalamo-hypophysial portal vasculature, travel to the anterior pituitary gland and stimulate or inhibit secretion of adenohypophysial hormones. Secretion of hypothalamic hormones is ultimately controlled by a variety of neurotransmitters and neuropeptides, the most studied in swine being the endogenous opioid peptides (EOP) and more recently, the excitatory amino acids (ExAA). In general, EOP inhibit GnRH and hence LH secretion, and this effect involves the central catecholaminergic system. A definitive role for EOP in the modulation of FSH release remains to be determined. EOP stimulate secretion of GHRH and thus growth hormone release, and depending on the animal model studied, EOP exert either stimulatory or inhibitory influences on prolactin secretion. ExAA, working via N-methyl-D-aspartate (NMDA) receptors at the central nervous system, stimulate secretion of LH, FSH, growth hormone and prolactin in appropriate animal models. However, in certain situations, an inhibitory effect of ExAA on LH secretion has been demonstrated. The modulation of growth hormone and prolactin secretion by ExAA involves EOP. Research investigating the function of ExAA and EOP in the physiological control of swine reproduction warrants further scrutiny.
神经肽和氨基酸在控制猪脑垂体前叶激素分泌中的作用。
所有生殖过程都涉及垂体前叶分泌的一种或多种蛋白质激素:LH, FSH,催乳素,生长激素,ACTH和促甲状腺激素(TSH)。生殖的主要激素,如黄体生成素和卵泡刺激素,直接调节生殖活动。例如,黄体生成素和卵泡刺激素刺激母猪卵泡生长和雌二醇的相关分泌。相反,生殖的次级激素,如TSH,是允许的,并调节其他生理系统,间接但深刻地影响生殖。猪的繁殖可以通过发展策略来改变和控制垂体前叶激素的分泌来提高。然而,成功地操纵腺垂体激素的分泌需要对控制下丘脑-垂体轴功能的机制有充分的了解。下丘脑激素包括GnRH、多巴胺、生长激素释放激素(GHRH)、生长抑素、促肾上腺皮质激素释放激素(CRH)和甲状腺激素释放激素(TRH)在核周围合成,核周围具有终止于中隆起的轴突。这些激素被释放到下丘脑-垂体门静脉系统,到达垂体前叶,刺激或抑制腺垂体激素的分泌。下丘脑激素的分泌最终由多种神经递质和神经肽控制,在猪体内研究最多的是内源性阿片肽(EOP)和最近研究的兴奋性氨基酸(ExAA)。一般来说,EOP抑制GnRH,从而抑制黄体生成素分泌,这种作用涉及中枢儿茶酚胺能系统。EOP在调节FSH释放中的确切作用仍有待确定。EOP刺激GHRH的分泌,从而促进生长激素的释放,并且根据所研究的动物模型,EOP对催乳素分泌有刺激或抑制作用。ExAA通过中枢神经系统的n -甲基- d -天冬氨酸(NMDA)受体起作用,在适当的动物模型中刺激黄体生成素、卵泡刺激素、生长激素和催乳素的分泌。然而,在某些情况下,ExAA对LH分泌的抑制作用已被证明。ExAA对生长激素和催乳素分泌的调节涉及EOP。研究ExAA和EOP在猪繁殖生理控制中的作用值得进一步研究。
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