Nakamura Urara, Rudolf Faidiban O, Pandey Kiran, Kadokawa Hiroya
Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi-shi, Yamaguchi-ken 1677-1, Japan.
Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi-shi, Yamaguchi-ken 1677-1, Japan.
Anim Reprod Sci. 2015 May;156:118-27. doi: 10.1016/j.anireprosci.2015.03.009. Epub 2015 Mar 21.
Picomolar concentrations of estradiol produce rapid suppression of GnRH-induced luteinizing hormone (LH) secretion from the anterior pituitary (AP) of cattle via G-protein-coupled receptor 30 (GPR30). Zeranol is a strong estrogenic metabolite derived from zearalenone, a non-steroidal mycoestrogen produced by Fusarium that induces reproductive disorders in domestic animals. The hypothesis was tested that zeranol suppresses GnRH-induced LH release from the AP of cattle via GPR30 in a rapid, non-genomic manner. The AP cells (n=15) were cultured for 3 days in steroid-free conditions and then treated them with estradiol (0.001-10nM) or zeranol (0.001-100nM) for 5min before GnRH stimulation. Pre-treatment with 0.001-0.1nM estradiol suppressed GnRH-stimulated LH secretion. Pre-treatment with zeranol at concentrations of 0.001nM (P<0.01), 0.01nM (P<0.01), 0.1nM (P<0.05), and 1nM (P<0.05), but not at concentrations of 10 and 100nM, also inhibited GnRH-stimulated LH secretion from AP cells. Pre-treatment for 5min with a GPR30-specific antagonist, G36, inhibited estradiol or zeranol suppression of LH secretion from cultured AP cells. Cyclic AMP measurements and quantitative PCR analyses revealed that pre-treatment with small amounts of estradiol (P<0.05) or zeranol (P<0.01) decreased cAMP, but not gene expressions of the LHα, LHβ, or FSHβ subunits in the AP cells. Hence, zeranol may suppress luteinizing hormone secretion from the AP of cattle via GPR30 in a rapid, non-genomic manner.
皮摩尔浓度的雌二醇通过G蛋白偶联受体30(GPR30)迅速抑制牛垂体前叶(AP)中促性腺激素释放激素(GnRH)诱导的促黄体生成素(LH)分泌。玉米赤霉醇是一种源自玉米赤霉烯酮的强效雌激素代谢物,玉米赤霉烯酮是镰刀菌产生的一种非甾体类霉菌雌激素,可在家畜中诱发生殖紊乱。本研究验证了一个假设,即玉米赤霉醇通过GPR30以快速、非基因组的方式抑制牛垂体前叶中GnRH诱导的LH释放。将垂体前叶细胞(n = 15)在无类固醇条件下培养3天,然后在GnRH刺激前用雌二醇(0.001 - 10 nM)或玉米赤霉醇(0.001 - 100 nM)处理5分钟。用0.001 - 0.1 nM雌二醇预处理可抑制GnRH刺激的LH分泌。用0.001 nM(P < 0.01)、0.01 nM(P < 0.01)、0.1 nM(P < 0.05)和1 nM(P < 0.05)浓度的玉米赤霉醇预处理也能抑制垂体前叶细胞中GnRH刺激的LH分泌,但10和100 nM浓度时则不能。用GPR30特异性拮抗剂G36预处理5分钟可抑制培养的垂体前叶细胞中雌二醇或玉米赤霉醇对LH分泌的抑制作用。环磷酸腺苷(cAMP)测量和定量聚合酶链反应(PCR)分析表明,用少量雌二醇(P < 从垂体前叶细胞中GnRH刺激的LH分泌。用GPR30特异性拮抗剂G36预处理5分钟可抑制培养的垂体前叶细胞中雌二醇或玉米赤霉醇对LH分泌的抑制作用。环磷酸腺苷(cAMP)测量和定量聚合酶链反应(PCR)分析表明,用少量雌二醇(P < 0.05)或玉米赤霉醇(P < 0.01)预处理可降低cAMP水平,但不会降低垂体前叶细胞中LHα、LHβ或FSHβ亚基的基因表达。因此,玉米赤霉醇可能通过GPR30以快速、非基因组的方式抑制牛垂体前叶的促黄体生成素分泌。 0.05)或玉米赤霉醇(P < 0.01)预处理可降低cAMP水平,但不会降低垂体前叶细胞中LHα、LHβ或FSHβ亚基的基因表达。因此,玉米赤霉醇可能通过GPR30以快速、非基因组的方式抑制牛垂体前叶的促黄体生成素分泌。