Estienne M J, Harter-Dennis J M, Barb C R
Department of Agriculture, University of Maryland Eastern Shore, Princess Anne 21853, USA.
J Reprod Fertil Suppl. 1997;52:3-17.
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.
促黄体生成素(LH)、促卵泡生成素(FSH)、催乳素、生长激素、促肾上腺皮质激素(ACTH)和促甲状腺激素(TSH)。生殖的主要激素,如LH和FSH,直接调节生殖活动。例如,LH和FSH刺激母猪卵泡生长及相关的雌二醇分泌。相比之下,生殖的次要激素,如TSH,具有允许作用,并调节其他间接但深刻影响生殖的生理系统。通过制定改变和控制腺垂体激素分泌的策略,可以提高猪的繁殖能力。然而,成功操纵腺垂体激素分泌需要深入了解控制下丘脑 - 垂体轴功能的机制。下丘脑激素包括促性腺激素释放激素(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)和促甲状腺激素释放激素(TRH),它们在具有轴突的神经细胞体中合成,这些轴突终止于正中隆起。这些激素释放到下丘脑 - 垂体门脉血管系统中,输送到腺垂体并刺激或抑制腺垂体激素的分泌。下丘脑激素的分泌最终受多种神经递质和神经肽控制,在猪中研究最多的是内源性阿片肽(EOP),最近还有兴奋性氨基酸(ExAA)。一般来说,EOP抑制GnRH从而抑制LH分泌,这种作用涉及中枢儿茶酚胺能系统。EOP在调节FSH释放中的明确作用尚待确定。EOP刺激GHRH分泌从而促进生长激素释放,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通过中枢神经系统中的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LH、FSH、生长激素和催乳素的分泌。然而,在某些情况下,已证明ExAA对LH分泌有抑制作用。ExAA对生长激素和催乳素分泌的调节涉及EOP。研究ExAA和EOP在猪生殖生理控制中的功能值得进一步深入研究。