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氟比洛芬抑制大鼠未成熟莱迪希细胞的雄激素产生。

Flurbiprofen Inhibits Androgen Productions in Rat Immature Leydig Cells.

机构信息

Department of Anesthesiology , The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University , Wenzhou , Zhejiang 325027 , People's Republic of China.

Department of Pathology , The Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University , Wenzhou , Zhejiang 325035 , People's Republic of China.

出版信息

Chem Res Toxicol. 2019 Aug 19;32(8):1504-1514. doi: 10.1021/acs.chemrestox.8b00404. Epub 2019 Jul 8.

Abstract

Flurbiprofen is one of the nonsteroidal anti-inflammatory drugs. Whether flurbiprofen affects androgen biosynthesis in Leydig cells is still unknown. Immature Leydig cells (ILCs) isolated from 35-day-old male Sprague-Dawley rats were cultured with 0-100 μM flurbiprofen for 24 h and medium androgen levels and Leydig cell mRNA levels were measured. Immature Leydig cells were also incubated with 100 μM flurbiprofen for 3 h in combination with luteinizing hormone (LH), 8bromo-cAMP, 22R-OH-cholesterol, pregnenolone, progesterone, androstenedione, testosterone, and dihydrotestosterone, respectively, and medium androgen levels were measured. The ROS generation and apoptosis rate were also investigated. The direct effects of flurbiprofen on androgen biosynthetic and metabolizing enzyme activities were measured. Flurbiprofen significantly inhibited basal, LH, and 8bromo-cAMP stimulated androgen production at 10 and 100 μM. Further study demonstrated that flurbiprofen competitively inhibited rat and human testis 3β-hydroxysteroid dehydrogenase (HSD3B) activity with the half maximal inhibitory concentration (IC) values of 0.95 μM for rat enzyme and 6.31 μM for human enzyme. In addition, flurbiprofen down-regulated the expression of and at 1, 10, and 100 μM. Flurbiprofen also down-regulated expression at 100 μM. Flurbiprofen at 10 and 100 μM increased ROS production and apoptosis rate of rat Leydig cells. In conclusion, flurbiprofen directly inhibits HSD3B activity and the expression levels of and in rat Leydig cells, thus leading to the reduction of androgen secretion.

摘要

氟比洛芬是一种非甾体抗炎药。氟比洛芬是否影响睾丸间质细胞中的雄激素生物合成尚不清楚。将 35 日龄雄性 Sprague-Dawley 大鼠分离的未成熟睾丸间质细胞(ILCs)用 0-100μM 氟比洛芬培养 24 小时,并测量培养基中雄激素水平和睾丸间质细胞 mRNA 水平。未成熟的睾丸间质细胞也与黄体生成素(LH)、8-溴-cAMP、22R-OH-胆固醇、孕烯醇酮、孕酮、雄烯二酮、睾酮和二氢睾酮分别孵育 100μM 氟比洛芬 3 小时,并测量培养基中雄激素水平。还研究了 ROS 生成和细胞凋亡率。测量了氟比洛芬对雄激素生物合成和代谢酶活性的直接影响。氟比洛芬在 10 和 100μM 时显著抑制基础、LH 和 8-溴-cAMP 刺激的雄激素产生。进一步的研究表明,氟比洛芬竞争性抑制大鼠和人睾丸 3β-羟甾类脱氢酶(HSD3B)活性,大鼠酶的半最大抑制浓度(IC)值为 0.95μM,人酶为 6.31μM。此外,氟比洛芬在 1、10 和 100μM 时下调 和 的表达。氟比洛芬还下调 100μM 时的表达。氟比洛芬在 10 和 100μM 时增加大鼠睾丸间质细胞的 ROS 生成和细胞凋亡率。总之,氟比洛芬直接抑制大鼠睾丸间质细胞中的 HSD3B 活性和 、 和 的表达水平,从而导致雄激素分泌减少。

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