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去势和衰老诱导大鼠前列腺中锌转运蛋白和金属硫蛋白表达的变化。

Castration- and aging-induced changes in the expression of zinc transporter and metallothionein in rat prostate.

作者信息

Iguchi Kazuhiro, Morihara Naoaki, Usui Shigeyuki, Hayama Minoru, Sugimura Yoshiki, Hirano Kazuyuki

机构信息

Laboratory of Pharmaceutics, Gifu Pharmaceutical University, 1-25-4 Daigaku-nishi, Gifu 501-1196, Japan.

出版信息

J Androl. 2011 Mar-Apr;32(2):144-50. doi: 10.2164/jandrol.110.011205. Epub 2010 Aug 26.

Abstract

Prostate tissue contains high concentrations of zinc. Zinc content in the prostate gland changes in prostatic disease, such as benign prostate hyperplasia and prostate cancer, which occur more frequently with increasing age. Prostate zinc content is also known to decrease after castration in animal models. It is not clear how prostate zinc content is regulated; therefore, to clarify the mechanisms underlying zinc homeostasis, we examined zinc content and the expression of zinc transporters and metallothioneins in the prostates of aged or castrated rats. Zinc concentration was measured by flame atomic absorption spectrometry. The mRNA expression of zinc transporters and metallothioneins was determined by real-time reverse transcriptase polymerase chain reaction analysis. The expression of the zinc transporter Slc30a2 (Znt2) in ventral prostate (VP) of aged rats (21 months) was approximately 21-fold higher than that in VP of young rats (4 months), and zinc levels in VP of young rats increased significantly compared with that in aged rats. Zinc content in lateral prostate (LP) and dorsal prostate did not differ between young and aged rats. Decreased metallothionein-3 (Mt3) expression was observed in LP of castrated rats, and this reduction was prevented by testosterone replacement. Zinc content and Mt3 expression levels correlated significantly in rat LP. Our findings suggest that Mt3 could play a critical role in zinc homeostasis in rat LP.

摘要

前列腺组织含有高浓度的锌。在前列腺疾病如良性前列腺增生和前列腺癌中,前列腺中的锌含量会发生变化,这些疾病随着年龄增长而更频繁地出现。在动物模型中,已知去势后前列腺锌含量会降低。目前尚不清楚前列腺锌含量是如何调节的;因此,为了阐明锌稳态的潜在机制,我们检测了老年或去势大鼠前列腺中的锌含量以及锌转运体和金属硫蛋白的表达。通过火焰原子吸收光谱法测量锌浓度。通过实时逆转录聚合酶链反应分析确定锌转运体和金属硫蛋白的mRNA表达。老年大鼠(21个月)腹侧前列腺(VP)中锌转运体Slc30a2(Znt2)的表达比年轻大鼠(4个月)VP中的表达高约21倍,并且年轻大鼠VP中的锌水平与老年大鼠相比显著增加。年轻和老年大鼠的侧叶前列腺(LP)和背叶前列腺中的锌含量没有差异。在去势大鼠的LP中观察到金属硫蛋白-3(Mt3)表达降低,并通过睾酮替代阻止了这种降低。大鼠LP中的锌含量与Mt3表达水平显著相关。我们的研究结果表明,Mt3可能在大鼠LP的锌稳态中起关键作用。

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