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[血红素加氧酶2在去势大鼠阴茎海绵体中的表达]

[Expression of heme oxygenase 2 in the corpus cavernosum of castrated rats].

作者信息

Deng Qing-fu, Jiang Rui, Zhu Ping-yu, Wang Xiao-ran

机构信息

Department of Urology, the Affiliated Hospital of Luzhou Medical College, Luzhou, Sichuan 646000, China.

出版信息

Zhonghua Nan Ke Xue. 2008 Jun;14(6):503-6.

PMID:18649746
Abstract

OBJECTIVE

To determine the expressions of HO-2 and eNOS in the corpus cavernosum of castrated rats and investigate the correlation of HO-2 and eNOS with erectile dysfunction.

METHODS

Forty SD rats of 10 weeks were equally divided into 3 castrated groups (4, 8 and 12 weeks respectively after removal of bilateral testes) and a sham operation control group. All the rats were detected for serum testosterone (T), intracavernosal pressure (ICP) and mean arterial blood pressure (MAP) 2, 8 and 12 weeks after the surgery, the content of HO-2 analyzed by Western blot and the expressions of eNOS and HO-2 determined by immunohistochemistry.

RESULTS

Testosterone level and ICP/MAP ratio were markedly decreased after the castration (P < 0.05). The HO-2 expression was detected in the corpus cavernosum of all but the 12-week castrated rats, and the area under the curve was (341.50 +/- 99.70) in the 4-week castrated group, significantly less than in the 8-week (705.00 +/- 152. 74) and the control group (876 +/- 443. 36) (P < 0. 05), with no obvious difference between the latter two. eNOS was found mainly in the vascular endothelial cells of the corpus cavernosum, significantly less in the castrated (123.94 +/- 30. 23) than in the control group (421.21 +/- 125. 12).

CONCLUSION

Androgens might mediate the penile erectile function through HO-2 and eNOS in the corpus cavernosum of rats.

摘要

目的

检测去势大鼠阴茎海绵体内血红素加氧酶-2(HO-2)和内皮型一氧化氮合酶(eNOS)的表达,探讨HO-2、eNOS与勃起功能障碍的相关性。

方法

将40只10周龄的SD大鼠平均分为3个去势组(分别于双侧睾丸切除后4、8和12周)和1个假手术对照组。术后2、8和12周检测所有大鼠的血清睾酮(T)、海绵体内压(ICP)和平均动脉血压(MAP),采用蛋白质免疫印迹法分析HO-2含量,免疫组织化学法检测eNOS和HO-2的表达。

结果

去势后睾酮水平及ICP/MAP比值明显降低(P<0.05)。除12周去势组外,其余各组阴茎海绵体均检测到HO-2表达,4周去势组曲线下面积为(341.50±99.70),明显低于8周去势组(705.00±152.74)和对照组(876±443.36)(P<0.05),后两者差异无统计学意义。eNOS主要分布于阴茎海绵体血管内皮细胞,去势组(123.94±30.23)明显低于对照组(421.21±125.12)。

结论

雄激素可能通过大鼠阴茎海绵体内的HO-2和eNOS介导阴茎勃起功能。

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