The Effect of Xialiqi Capsule on Testosterone-Induced Benign Prostatic Hyperplasia in Rats

被引:22
作者
Cai, Hongcai [1 ,2 ]
Zhang, Guowei [1 ]
Yan, Zechen [3 ]
Shang, Xuejun [1 ]
机构
[1] Southern Med Univ, Jinling Hosp, Dept Androl, Nanjing 210002, Jiangsu, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Ctr Reprod Med, Family Planning Res Inst, Wuhan 430030, Hubei, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Surg, Zhengzhou 450052, Henan, Peoples R China
关键词
URINARY-TRACT SYMPTOMS; CELL-PROLIFERATION; INFLAMMATORY RESPONSE; ERECTILE DYSFUNCTION; OXIDATIVE STRESS; ASTRAGALI RADIX; HERBAL FORMULA; IN-VITRO; EXTRACT; DIHYDROTESTOSTERONE;
D O I
10.1155/2018/5367814
中图分类号
R [医药、卫生];
学科分类号
100218 [急诊医学];
摘要
Benign prostatic hyperplasia (BPH) is common among elderly men, of which inflammation, oxidative stress, proliferative, and apoptotic changes play important roles. Xialiqi (XLQ) capsule, a traditional Chinese herbal formula, is used as a potential drug in treating BPH. This study aims to evaluate the therapeutic effect of XLQ capsule on testosterone propionate-(TP-) induced BPH in rats. Fifty male Sprague-Dawley rats were randomly divided into 5 groups: sham control, BPH model, high and low dose of XLQ, and finasteride as a positive control group. All groups were treated with appropriate drugs/normal saline for 28 consecutive days. Prostate weights were recorded; histopathological changes and content of IL-8, TNF-alpha, DHT, SOD, MDA, caspase-3, and PCNA of the prostate were determined. Animals with BPH demonstrated significantly increased prostate weights and prostate index, higher levels of IL-8, TNF-alpha, DHT, MDA, and PCNA, but lower activity of SOD and reduced expression of caspase-3. After treatment with XLQ, significant reductions of prostate weights, prostate index, IL-8, TNF-alpha, DHT, MDA, and PCNA, increased activity of SOD, and higher level of caspase-3 were shown. The present study indicates that XLQ can effectively prevent the development of TP-induced BPH model through mechanisms of anti-inflammation, antioxidation, antiproliferation, and proapoptosis.
引用
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页数:9
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