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[通过挤压损伤或切除海绵体神经建立前列腺癌根治术后勃起功能障碍大鼠模型]

[Establishment of a rat model of erectile dysfunction after radical prostatectomy by crush injury or resection of the cavernous nerve].

作者信息

Bian Jun, Dai Yu-ping, Sun Xiang-zhou, Liu Gui-hua, Deng Chun-hua, Ye Yun-lin

机构信息

Department of Urology, First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2011 Feb;31(2):230-3.

PMID:21354899
Abstract

OBJECTIVE

To establish a rat model mimicking erectile dysfunction following radical prostatectomy by crush injury or reaction of the cavernous nerve (CN).

METHODS

Thirty rats were randomized into CN crush group, CN resection group and sham-operated group. Four weeks after surgery, the rat models were evaluated by apomorphine test and ICP/MAP measurement. Fluorogold (FG) retrograde tracer was used to assess the CN injury. The penile tissues were then harvested for immunohistochemical detection of the nNOS-positive fibers to evaluate the CN injury.

RESULTS

The rats in CN crush group and CN resection group exhibited erectile dysfunction in apomorphine test or in response to electrical stimulation of the ganglion stellatum (MPG). In the sham-operated group, the rats showed normal erectile function with increased ICP/MAP following electrical stimulation (P<0.05). Immunohistochemistry revealed reduced nNOS-positive fibers in both CN crush group and CN resection group as compared with those in the sham-operated group (P<0.05), showing no significant difference between the former two groups (P>0.05). The FG-positive MPG cells in CN crush group and CN resection group were significantly less than that in the sham-operated group (P<0.05), and the positive cells were even less in CN resection group (P<0.05).

CONCLUSION

The rat CN is structurally similar to human CN, and crush injury and resection of the CN are both reliable methods for establishing rat models of erectile dysfunction following radical prostatectomy.

摘要

目的

通过海绵体神经(CN)挤压损伤或切断建立模拟前列腺癌根治术后勃起功能障碍的大鼠模型。

方法

将30只大鼠随机分为CN挤压组、CN切断组和假手术组。术后4周,通过阿扑吗啡试验和平均动脉压/海绵体内压(ICP/MAP)测量对大鼠模型进行评估。使用荧光金(FG)逆行示踪剂评估CN损伤。然后采集阴茎组织进行nNOS阳性纤维的免疫组织化学检测,以评估CN损伤。

结果

CN挤压组和CN切断组的大鼠在阿扑吗啡试验或对星状神经节(MPG)电刺激的反应中表现出勃起功能障碍。在假手术组中,大鼠在电刺激后勃起功能正常,ICP/MAP升高(P<0.05)。免疫组织化学显示,与假手术组相比,CN挤压组和CN切断组的nNOS阳性纤维均减少(P<0.05),前两组之间无显著差异(P>0.05)。CN挤压组和CN切断组的FG阳性MPG细胞明显少于假手术组(P<0.05),CN切断组的阳性细胞更少(P<0.05)。

结论

大鼠CN在结构上与人CN相似,CN挤压损伤和切断都是建立前列腺癌根治术后勃起功能障碍大鼠模型的可靠方法。

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