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槟榔碱对大鼠睾酮释放的影响。

Effects of arecoline on testosterone release in rats.

作者信息

Wang Shyi-Wu, Hwang Guey-Shyang, Chen Te-Jung, Wang Paulus S

机构信息

Department of Physiology, School of Medicine, Chang Gung University, Kweisan, Taoyuan, Taiwan, ROC.

出版信息

Am J Physiol Endocrinol Metab. 2008 Aug;295(2):E497-504. doi: 10.1152/ajpendo.00045.2008. Epub 2008 Jun 17.

Abstract

Arecoline is one of the major components of betel nuts, which have been consumed as chewing gum in Southeast Asia. In this study, the effects of arecoline on testosterone (T) secretion were explored. Male rats were injected with human chorionic gonadotropin (hCG, 5 IU/kg) or arecoline (1 microg/kg) plus hCG via a jugular catheter. Blood samples were collected at several time intervals subsequent to the challenge. Rat anterior pituitary was treated with gonadotropin-releasing hormone in vitro with or without arecoline, and then the concentrations of luteinizing hormone (LH) in the medium were measured. Rat Leydig cells were purified by Percoll density gradient centrifugation and incubated with arecoline, hCG, forskolin, 8-bromo-cAMP (8-Br-cAMP), nifedipine, nimodipine, or tetrandrine at 34 degrees C for 1 h. A single intravenous injection of arecoline resulted in an increase of the hCG-induced level of plasma T. Administration of arecoline (10(-8) to 10(-6) M) in vitro increased T production in Leydig cells. The stimulatory effect of arecoline on T release in vitro was enhanced by hCG (0.001 IU/ml), forskolin (10(-6) M), or 8-Br-cAMP (10(-5) M). By contrast, nifedipine, nimodipine, or tetrandrine inhibited the increased T concentrations induced by arecoline. Western blot showed that arecoline increases steroidogenic acute regulatory (StAR) protein expression compared with vehicle. These results suggested that arecoline stimulates testosterone production by acting directly on Leydig cells via mechanisms involving an activation of L-type calcium channels, increasing the activity of 17beta-hydroxysteroid dehydrogenase and enhancing the expression of StAR.

摘要

槟榔碱是槟榔的主要成分之一,在东南亚地区,槟榔一直被当作口香糖咀嚼食用。在本研究中,我们探究了槟榔碱对睾酮(T)分泌的影响。通过颈静脉导管给雄性大鼠注射人绒毛膜促性腺激素(hCG,5 IU/kg)或槟榔碱(1微克/千克)加hCG。在注射后几个时间点采集血样。将大鼠垂体前叶在体外用促性腺激素释放激素处理,同时加入或不加入槟榔碱,然后测定培养基中促黄体生成素(LH)的浓度。通过Percoll密度梯度离心法纯化大鼠睾丸间质细胞,并将其与槟榔碱、hCG、福斯可林、8-溴环磷腺苷(8-Br-cAMP)、硝苯地平、尼莫地平或粉防己碱在34℃下孵育1小时。单次静脉注射槟榔碱会使hCG诱导的血浆T水平升高。在体外给予槟榔碱(10^-8至10^-6 M)可增加睾丸间质细胞中T的生成。hCG(0.001 IU/ml)、福斯可林(10^-6 M)或8-Br-cAMP(10^-5 M)可增强槟榔碱对体外T释放的刺激作用。相比之下,硝苯地平、尼莫地平或粉防己碱可抑制槟榔碱诱导的T浓度升高。蛋白质免疫印迹法显示,与赋形剂相比,槟榔碱可增加类固醇生成急性调节蛋白(StAR)的表达。这些结果表明,槟榔碱通过直接作用于睾丸间质细胞来刺激睾酮生成,其作用机制包括激活L型钙通道、增加17β-羟类固醇脱氢酶的活性以及增强StAR的表达。

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