Li Li, Dai Ning, Na Sha, Jia Hui-Yu, Zhou Xue-Chun, Zhou Di-di, Wang Tong-Sheng
Department of Pharmacology, Anhui University of Chinese Medicine, Anhui University of Chinese Medicine, Hefei, Anhui 230038, China.
Department of Andrology, Anhui Provincial Hospital of Chinese Medicine, Anhui University of Chinese Medicine, Hefei, Anhui 230038, China.
Zhonghua Nan Ke Xue. 2016 Sep;22(9):827-833.
To investigate the protective effect of Wuziyanzong Pills (WYP) in the rat model of oligoasthenospermia (OAS) and its action mechanism.
Sixty male SD rats were equally randomized into six groups: normal control, OAS model, Shengjing Capsules (1.6 g per kg of the body weight), low-dose WYP (1 g per kg of the body weight), medium-dose WYP (2 g per kg of the body weight), and high-dose WYP (4 g per kg of the body weight). The OAS model was established by intragastric administration of Tripterygium glucoside at 30 mg per g per d for 6 weeks. From the 3rd week of modeling, the rats of the medication groups were treated intragastrically with corresponding drugs for 4 weeks. Then all the rats were sacrificed for measurement of the testicular and epididymal organ coefficients, examination of epididymal sperm quality and apoptosis, and detection of the openness of the sperm mitochondrial permeability transition pore (MPTP). Histopathological changes in the testis were observed by HE staining and the apoptosis of spermatogenic cells determined by Hochest staining.
WYP obviously improved the organ coefficients of the testis and epididymis, increased sperm concentration, motility and viability, decreased the apoptosis of spermatogenic cells, and inhibited the abnormal openness of MPTP in the OAS model rats. HE staining showed that the number and levels of spermatogenic cells were significantly increased while Hochest staining manifested that the apoptosis of spermatogenic cells was remarkably inhibited in the seminiferous tubules of the testis in the WYP-treated rats.
WYP can improve sperm quality and reduce the apoptosis of spermatogenic cells (including sperm) in OAS model rats, which may be related with its inhibitory effect on the abnormal openness of MPTP.
探讨五子衍宗丸(WYP)对少弱精子症(OAS)大鼠模型的保护作用及其作用机制。
将60只雄性SD大鼠随机分为6组:正常对照组、OAS模型组、生精胶囊组(1.6 g/kg体重)、低剂量WYP组(1 g/kg体重)、中剂量WYP组(2 g/kg体重)和高剂量WYP组(4 g/kg体重)。通过每日灌胃给予雷公藤多苷30 mg/g,连续6周建立OAS模型。从建模第3周起,给药组大鼠灌胃相应药物4周。然后处死所有大鼠,测量睾丸和附睾脏器系数,检测附睾精子质量和凋亡情况,检测精子线粒体通透性转换孔(MPTP)的开放情况。通过HE染色观察睾丸组织病理学变化,用Hochest染色法检测生精细胞凋亡。
WYP明显改善了OAS模型大鼠睾丸和附睾的脏器系数,提高了精子浓度、活力和存活率,降低了生精细胞凋亡率,并抑制了MPTP的异常开放。HE染色显示,WYP处理组大鼠睾丸生精细胞数量和层次显著增加,Hochest染色表明生精细胞凋亡明显受到抑制。
WYP可改善OAS模型大鼠的精子质量,减少生精细胞(包括精子)凋亡,这可能与其对MPTP异常开放的抑制作用有关。