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辛伐他汀对自发性高血压大鼠前列腺增生的影响及病理生理机制

Influence and pathophysiological mechanisms of simvastatin on prostatic hyperplasia in spontaneously hypertensive rats.

作者信息

Zhang Xiangyu, Shen Fang, Dong Lini, Zhao Xiaokun, Qu Xiaobing

机构信息

Departments of Geriatrics and Urology, Second Xiangya Hospital of Central South University, Changsha, Hunan, P.R. China.

出版信息

Urol Int. 2013;91(4):467-73. doi: 10.1159/000350519. Epub 2013 Jul 6.

DOI:10.1159/000350519
PMID:23838355
Abstract

OBJECTIVE

To explore the effects and mechanisms of simvastatin on prostate hyperplasia in spontaneously hypertensive rats (SHRs).

METHODS

Thirty-six male SHRs were randomly divided into three groups: the 10 and the 20 mg/kg/d simvastatin group and the control group. After 6 weeks the ultra-microscopic prostate structures were observed. The serum levels of interleukin-6 (IL-6), insulin-like growth factor (IGF-1) and angiotensin II (Ang-II) were measured by enzyme-linked immunosorbent assays. The endothelium-derived nitric oxide synthase (eNOS) expression was evaluated with immunohistochemistry.

RESULTS

Compared to the control group, the 20 mg/kg/d simvastatin group presented with lower absolute (p = 0.005) and relative prostate weight (p = 0.009). The basal cells and columnar cells presented with edema, condensed heterochromatin in interstitial fibroblast nuclei, widened nucleus gaps, and decreased mitochondria and endoplasmic reticulum in the 10 mg/kg/d simvastatin group, these changes were more pronounced in the 20 mg/kg/d simvastatin group. The IL-6 levels in the 10 and 20 mg/kg/d simvastatin groups were lower than those of the controls (p = 0.005 and p = 0.008). The IGF-1 levels of the 20 mg/kg/d simvastatin group were reduced compared to the control group (p = 0.016).

CONCLUSIONS

Simvastatin can delay and inhibit prostatic hyperplasia and progression in SHR. These actions may be mediated through the suppression of inflammatory and growth factors.

摘要

目的

探讨辛伐他汀对自发性高血压大鼠(SHR)前列腺增生的影响及其机制。

方法

将36只雄性SHR随机分为三组:10mg/kg/d和20mg/kg/d辛伐他汀组及对照组。6周后观察前列腺超微结构。采用酶联免疫吸附测定法检测血清白细胞介素-6(IL-6)、胰岛素样生长因子(IGF-1)和血管紧张素II(Ang-II)水平。用免疫组织化学法评估内皮型一氧化氮合酶(eNOS)表达。

结果

与对照组相比,20mg/kg/d辛伐他汀组的绝对前列腺重量(p = 0.005)和相对前列腺重量较低(p = 0.009)。10mg/kg/d辛伐他汀组的基底细胞和柱状细胞出现水肿,间质成纤维细胞核内异染色质浓缩,核间隙增宽,线粒体和内质网减少,这些变化在20mg/kg/d辛伐他汀组中更明显。10mg/kg/d和20mg/kg/d辛伐他汀组的IL-6水平低于对照组(p = 0.005和p = 0.008)。20mg/kg/d辛伐他汀组的IGF-1水平与对照组相比降低(p = 0.016)。

结论

辛伐他汀可延缓和抑制SHR的前列腺增生及进展。这些作用可能通过抑制炎症和生长因子来介导。

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Urol Int. 2013;91(4):467-73. doi: 10.1159/000350519. Epub 2013 Jul 6.
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