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首页> 外文期刊>General and comparative endocrinology >Effect of Naltrexone on photoperiodic regulation of testicular steroidogenesis in adult golden hamster, Mesocricetus auratus
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Effect of Naltrexone on photoperiodic regulation of testicular steroidogenesis in adult golden hamster, Mesocricetus auratus

机译:纳曲酮对成年金仓鼠中型睾丸激素光周期调节的影响

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Photoperiodic regulation of testicular steroidogenesis through modulation of MT1R expression and local melatonin content is well established. However, additional mediators besides local melatonergic system in photoperiodic control of testicular steroidogenesis in golden hamster have not been studied in detail. Endogenous opioid peptides (EOP) are known to regulate reproduction via acting at multiple levels of the hypothalamus-pituitary-gonadal (HPG) axis. The presence of beta-endorphin, a naturally occurring opioid peptide, and its receptor (mu-opioid receptor, mu OR) has been reported in rat testes; however the functional significance of photoperiodic regulation mu OR in testicular steroidogenesis is not clear. In the present study, we assessed the effect of Naltrexone (Nal), a mu OR antagonist, in photoperiodic regulation of testicular steroidogenesis. Immunohistochemical (IHC) localization and expression of mu OR along with the expression of steroidogenic markers in testes was analyzed through western blot analyses. IHC suggest immunoreactivity for mu OR in Leydig cells with strong immunoreactivity under SD (short-day) condition, whereas weak immunoreactivity was observed under LD (long-day). The expression of mu OR was significantly decreased following Nal administration in both the photoperiodic conditions. The localization and differential photoperiodic regulation of mu OR in Leydig cells suggests its involvement in testicular steroidogenesis. Further, Nal administration significantly increased the expression of steroidogenic markers (AR, StAR, P450(scc). LH-R, 3 beta-HSD and 17-HSD) and plasma testosterone concentration under SD condition as compared to SD-control. We may therefore suggest that photoperiod differentially regulates the expression of mu OR which thereby mediates the inhibitory effect of melatonin on testicular steroidogenesis. (C) 2015 Elsevier Inc. All rights reserved.
机译:通过调节MT1R表达和局部褪黑激素含量,对睾丸类固醇生成进行光周期调节已广为人知。然而,除了局部褪黑素能系统以外,还没有详细研究光周期控制金黄仓鼠睾丸类固醇生成的其他介质。已知内源性阿片肽(EOP)通过作用于下丘脑-垂体-性腺(HPG)轴的多个水平来调节生殖。已经在大鼠睾丸中报道了天然存在的阿片类肽β-内啡肽及其受体(μ阿片受体,μOR)的存在。然而,光周期调节μOR在睾丸类固醇生成中的功能意义尚不清楚。在本研究中,我们评估了mu OR拮抗剂纳曲酮(Nal)在睾丸类固醇生成的光周期调节中的作用。免疫组织化学(IHC)的定位和mu OR的表达以及类固醇生成标记在睾丸中的表达通过蛋白质印迹分析进行了分析。 IHC建议在SD(短日)条件下具有强免疫反应性的Leydig细胞对mu OR的免疫反应性,而在LD(长日)条件下则观察到弱的免疫反应性。在两种光周期条件下,Nal给药后,mu OR的表达均显着降低。 mu or OR在睾丸间质细胞中的定位和不同的光周期调节表明其参与睾丸类固醇生成。此外,与SD对照相比,Nal给药显着增加了在SD条件下类固醇生成标志物(AR,StAR,P450(scc),LH-R,3 beta-HSD和17-HSD)的表达和血浆睾丸激素浓度。因此,我们可能建议光周期差异调节mu OR的表达,从而介导褪黑激素对睾丸类固醇生成的抑制作用。 (C)2015 Elsevier Inc.保留所有权利。

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