Rudolf Faidiban Oktofianus, Kadokawa Hiroya
Joint Faculty of Veterinary Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi-shi, Yamaguchi 753-8511, Japan.
J Vet Med Sci. 2014 Dec;76(12):1623-5. doi: 10.1292/jvms.14-0179. Epub 2014 Aug 21.
STX is an agonist for a recently characterized membrane estrogen receptor whose structure has not been identified. We evaluated whether STX suppresses gonadotropin-releasing hormone (GnRH)-induced luteinizing hormone (LH) release from bovine anterior pituitary (AP) cells. We cultured AP cells (n=12) for 3 days in steroid-free conditions, followed by increasing concentrations (0.001, 0.01, 0.1, 1 and 10 nM) of 17β-estradiol or STX for 5 min before GnRH stimulation until the end of the experiment. Estradiol (0.001 to 0.1 nM) significantly suppressed GnRH-stimulated LH secretion, whereas STX did not affect GnRH-stimulated LH secretion at any of the tested concentrations. In conclusion, STX, unlike estradiol, possesses no suppressive effect on GnRH-induced LH release from bovine AP cells.
STX是一种作用于最近鉴定出的膜雌激素受体的激动剂,该受体的结构尚未明确。我们评估了STX是否能抑制促性腺激素释放激素(GnRH)诱导的牛垂体前叶(AP)细胞释放促黄体生成素(LH)。我们在无类固醇条件下将AP细胞(n = 12)培养3天,然后在GnRH刺激前5分钟,用递增浓度(0.001、0.01、0.1、1和10 nM)的17β-雌二醇或STX处理,直至实验结束。雌二醇(0.001至0.1 nM)显著抑制GnRH刺激的LH分泌,而在任何测试浓度下,STX均不影响GnRH刺激的LH分泌。总之,与雌二醇不同,STX对GnRH诱导的牛AP细胞LH释放没有抑制作用。