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促黄体生成素释放激素(LHRH)拮抗剂西曲瑞克注射后前列腺萎缩的机制:良性前列腺增生大鼠模型的实验研究

Mechanisms of prostate atrophy after LHRH antagonist cetrorelix injection: an experimental study in a rat model of benign prostatic hyperplasia.

作者信息

Yang Dong, Hou Teng, Yang Xiong, Ma Yan, Wang Longwang, Li Bing

机构信息

Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

Department of Urology, Shenzhen People's Hospital, Second Clinical Medical College, Jinan University, Shenzhen, 518020, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2012 Jun;32(3):389-395. doi: 10.1007/s11596-012-0067-x. Epub 2012 Jun 9.

Abstract

In the present study, we investigated the roles of TGF-β signaling pathway in a rat benign prostatic hyperplasia (BPH) model treated with cetrorelix. TGF-β1 and c-Myc expression were measured by qRT-PCR and Western blotting in the proximal and distal region of ventral prostatic lobes, respectively. We observed that treatment with cetrorelix led to a significant reduction of ventral prostate weight in a dose-dependent manner. In the proximal region, after cetrorelix treatment, the expression of TGF-β1 was dramatically increased (P<0.05), while the expression of c-Myc was significantly decreased (P<0.05). In comparison with the control group, the cetrorelix groups had more TUNEL-positive cells. Our findings strongly suggest that the TGF-β signaling pathway may be one of the major causes responsible for prostate volume reduction in BPH rats after cetrorelix treatment.

摘要

在本研究中,我们调查了转化生长因子-β(TGF-β)信号通路在使用西曲瑞克治疗的大鼠良性前列腺增生(BPH)模型中的作用。分别通过qRT-PCR和蛋白质免疫印迹法检测腹侧前列腺叶近端和远端区域的TGF-β1和c-Myc表达。我们观察到,西曲瑞克治疗导致腹侧前列腺重量以剂量依赖性方式显著降低。在近端区域,西曲瑞克治疗后,TGF-β1的表达显著增加(P<0.05),而c-Myc的表达显著降低(P<0.05)。与对照组相比,西曲瑞克组有更多TUNEL阳性细胞。我们的研究结果强烈表明,TGF-β信号通路可能是西曲瑞克治疗后BPH大鼠前列腺体积减小的主要原因之一。

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