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徐华, 黄洁, 李敏, 等. 小鼠睾丸体外培养模型研究邻苯二甲酸二(2-乙基己基)酯对睾酮合成及机制的影响[J]. 四川大学学报(医学版), 2013, 44(4): 511-516.
引用本文: 徐华, 黄洁, 李敏, 等. 小鼠睾丸体外培养模型研究邻苯二甲酸二(2-乙基己基)酯对睾酮合成及机制的影响[J]. 四川大学学报(医学版), 2013, 44(4): 511-516.
XU Hua, HUANG Jie, LI Min, et al. The Effects of Di-(2-ethylhexyl) Phthalate (DEHP) in Testosterone Synthesis and Its Molecular Mechanisms in the Fetal Testis of Male Mouse by Organ Culture in vitro[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(4): 511-516.
Citation: XU Hua, HUANG Jie, LI Min, et al. The Effects of Di-(2-ethylhexyl) Phthalate (DEHP) in Testosterone Synthesis and Its Molecular Mechanisms in the Fetal Testis of Male Mouse by Organ Culture in vitro[J]. Journal of Sichuan University (Medical Sciences), 2013, 44(4): 511-516.

小鼠睾丸体外培养模型研究邻苯二甲酸二(2-乙基己基)酯对睾酮合成及机制的影响

The Effects of Di-(2-ethylhexyl) Phthalate (DEHP) in Testosterone Synthesis and Its Molecular Mechanisms in the Fetal Testis of Male Mouse by Organ Culture in vitro

  • 摘要: 目的 探讨睾丸体外培养模型下邻苯二甲酸二(2-乙基己基)酯(DEHP)暴露对小鼠睾丸睾酮合成及基因表达的影响。 方法 用浸浴式一次性通气旋转装置体外培养小鼠睾丸组织。实验分为二甲基亚砜(DMSO)溶剂对照组和4个DEHP剂量染毒组(终浓度0.1、1.0、10.0、100.0 μmol/L)。分别培养24、48、72 h,每24 h通气一次。放射免疫法测定收集培养基中睾酮水平;Elisa法测定收集培养基中抑制素基因β_B基因(INHBβ)水平;实时荧光定量(QT)-PCR检测睾丸组织相关基因表达水平;HE染色观察睾丸组织病理学变化;免疫组化法检测睾丸组织相关蛋白表达。 结果 与DMSO溶剂对照组相比,DEHP一定浓度范围内,可使睾酮合成增加,但在DEHP 100.0 μmol/L染毒48、72 h,睾酮合成开始减少。Elisa测定INHBβ在DEHP 0.1 μmol/L、1.0 μmol/L染毒组合成增加,从DEHP 10.0 μmol/L开始合成减少。QT-PCR检测结果显示,与DMSO溶剂对照组相比,3β羟类固醇脱氢酶(3β-HSD)、抗细胞色素P450 17α羟化酶(P450c17)、细胞色素P450侧链裂解酶(P450Scc)、波形蛋白(vimentin)mRNA表达下降,尤其是DEHP 100.0 μmol/L剂量组(P<0.05),INHBβ mRNA表达无显著变化。HE染色,各组睾丸组织未观察到明显病理学改变。免疫组化检测结果显示,与DMSO溶剂对照组相比,蛋白3β-HSD、P450c17、P450Scc表达增强,vimentin表达减弱,尤其是DEHP 10.0 μmol/L、100.0 μmol/L两个剂量染毒组。 结论 DEHP暴露对体外培养睾丸的睾酮合成有影响,其机制可能由于其影响了相关功能基因表达,进而对睾酮合成产生正负调控两种作用。

     

    Abstract: Objective To investigate the effects of DEHP in testosterone synthesis and the related genes expression in the fetal testis of male mouse by organ culture in vitro. Methods The testis tissues were cultured in infiltrating type rotating device for 72 hours. The culture and gas were changed every 24 hours. The testis tissues were divided into the DMSO control group and four DEHP groups (the terminal concentration were 0.1, 1.0, 10.0, 100.0 μmol/L). The testosterone levels in the cultured medium were measured by radioimmunoassay, the INHBβ levels were measured by Elisa, the gene expressions related with testosterone synthesis were detected by real-time PCR, the morphological changes of cultured testis were observed by HE staining under optical microscope, the expressions of related proteins were measured by immunohistochemistry. Results Compared to the control group, the levels of testosterone synthesis in 0.1, 1.0, 10.0 μmol/L groups were increased, but decreased in 100.0 μmol/L group which were exposed in DEHP for 48 hours and 72 hours. There was an increase of INHBβ synthesis in 0.1 and 1.0 μmol/L groups, but a decrease in 10.0 and 100.0 μmol/L groups. The gene expressions of 3β-HSD, P450c17, P450Scc, vimentin were significantly decreased compared to that of control group especially in 1.0 and 10.0 μmol/L groups (P<0.05), but the expressions of INHBβ had no significant changes. There were no apparent morphological changes in testis tissue by HE staining. A significant increase of the three proteins (3β-HSD, P450c17, P450Scc) and a significant decrease of vimentin were observed in 10.0 and 100.0 μmol/L groups (P<0.05). Conclusion DEHP exposure can affect the testosterone synthesis in the fetal testis of male mouse. The regulation of gene expression involving in testosterone synthesis might be the mechanism.

     

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