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Localization and potential function of androgen receptor in rat salivary gland

机译:大鼠唾液腺中雄激素受体的定位及其潜在功能

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Aim: To investigate the localization and quantity of androgen receptor (AR) in the salivary glands of rats with further analysis on the effect of castration. Methods: Sixty male Wistar rats, aged 30-60 days, were randomly divided into three groups (castrated, sham-operated and normal controls) with 20 rats in each group. The rats in the castrated group were castrated and the submaxillary glands were removed after 1 week. The salivary glands of the rats in the sham-operated and the normal control groups were also removed. Parts of the salivary glands were fixed for immunohistochemistry and in situ hybridization assays. Other parts were used for Western blot. Results: AR immunoreactivity in the three groups was localized in the glandular epithelial cells of the serous acinus and the glandular duct of the salivary gland, mainly in the nuclei. AR mRNA hybridization signals in the salivary glands of the castrated group were mainly distributed in the epithelial cells of the convoluted and secretary ducts; AR mRNA in the sham-operated and the normal control groups were found in the epithelial cells of the convoluted, the secretary and the excretory ducts. The quantity of AR in the salivary glands was decreased significantly in the castrated rats compared with the sham-operated and the normal controls. Moreover, epidermal growth factor (EGF) secreted by the salivary glands was also decreased in the castrated rats. Conclusion: Castration appears to affect the production of AR in the salivary gland and the distribution of the AR mRNA and could further affect the function of the salivary gland. The changes of AR and the distribution of AR mRNA may play an important role in the interactions between the testes and the salivary gland.
机译:目的:探讨雄性激素受体(AR)在大鼠唾液腺中的定位和数量,并进一步分析去势作用。方法:将60只30-60天的雄性Wistar大鼠随机分为三组(cast割,假手术和正常对照组),每组20只。去势组大鼠去势,1周后摘除颌下腺。假手术组和正常对照组的大鼠唾液腺也被清除。唾液腺的一部分被固定用于免疫组织化学和原位杂交测定。其他部分用于蛋白质印迹。结果:三组的AR免疫反应性位于浆液性腺的腺上皮细胞和唾液腺的腺管中,主要在细胞核中。去势组唾液腺中的AR mRNA杂交信号主要分布在回旋管和秘书管的上皮细胞中;在假手术组和正常对照组中,AR mRNA在回旋管,秘书管和排泄管的上皮细胞中发现。与假手术组和正常对照组相比,the割的大鼠唾液腺中的AR含量明显降低。此外,去势大鼠的唾液腺分泌的表皮生长因子(EGF)也降低了。结论:去势似乎影响唾液腺中AR的产生和AR mRNA的分布,并可能进一步影响唾液腺的功能。 AR的变化和AR mRNA的分布可能在睾丸和唾液腺之间的相互作用中起重要作用。

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