Effects of N-carbamylglutamate and L-arginine on gonadotrophin-releasing hormone (GnRH) gene expression and secretion in GT1-7 cells
文献类型： 外文期刊
作者： Liu, Y. 1 ; Bai, J. H. 1 ; Xu, X. L. 1 ; Chen, Z. L. 1 ; Spicer, L. J. 2 ; Feng, T. 1 ;
作者机构： 1.Beijing Acad Agr & Forestry Sci, Inst Anim Husb & Vet Med, Beijing 100097, Peoples R China
2.Oklahoma State Univ, Dept Anim Sci, Stillwater, OK 74078 USA
关键词： cell culture; hormone secretion; hypothalamus
期刊名称：REPRODUCTION FERTILITY AND DEVELOPMENT （ 影响因子：2.311； 五年影响因子：2.396 ）
ISSN： 1031-3613
年卷期： 2018 年 30 卷 5 期
页码：
收录情况： SCI
摘要： Recent studies have shown that N-carbamylglutamate (NCG) and arginine (ARG) supplementation improves reproductive performance in livestock. The objectives of the present study were to evaluate the effects of NCG and ARG on GT1-7 cell gonadotrophin-releasing hormone (GnRH) secretion, gene expression and cell proliferation. GT1-7 cells were treated in vitro with different concentrations of NCG (0-1.0 mM) or ARG (0-4.0 mM) in serum-free medium for 12 or 24 h. For GnRH secretion and cell proliferation, GT1-7 cells were more sensitive to NCG than ARG. NCG treatment after 12 h increased cell numbers and inhibited GnRH secretion in a dose-dependent manner (P < 0.05), although there was no significant effect of NCG on these parameters after 24 h culture. ARG treatment decreased GnRH secretion after 24 h (P, 0.05), whereas it had no effect after 12 h. GT1-7 cells express GnRH, Kiss-1 metastasis-suppressor (Kiss1), G-protein coupled receptor 54 (GPR54), neuronal nitric oxide synthase (nNOS) and estrogen receptor a (ER alpha) genes. High concentrations of NCG (1.0 mM) and ARG (4.0 mM) inhibited (P < 0.05) GnRH and nNOS mRNA abundance in GT1-7 cells. ARG treatment decreased Kiss1 and increased ERa mRNA abundance. Thus, high concentrations of NCG (1.0 mM) and ARG (4.0 mM) may act both directly and indirectly to regulate GnRH neuron function by downregulating genes related to GnRH synthesis and secretion to slow GnRH production while stimulating GT1-7 cell proliferation.
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