Protective effect of Wuziyanzong Pills on rats with experimental oligoasthenospermia and its action mechanism.
- Author:
Li LI
1
;
Ning DAI
2
;
Sha NA
3
;
Hui-Yu JIA
1
;
Xue-Chun ZHOU
1
;
Di-di ZHOU
1
;
Tong-Sheng WANG
1
Author Information
- Publication Type:Journal Article
- Keywords: Wuziyanzong Pills; mitochondrial permeability transition pore; oligoasthenospermia; sperm apoptosis; sperm quality
- MeSH: Animals; Apoptosis; drug effects; Asthenozoospermia; chemically induced; drug therapy; Drugs, Chinese Herbal; pharmacology; Epididymis; drug effects; Male; Mitochondrial Membrane Transport Proteins; drug effects; Oligospermia; drug therapy; Random Allocation; Rats; Rats, Sprague-Dawley; Sperm Count; Sperm Motility; drug effects; Spermatozoa; cytology; drug effects; Testis; drug effects; Tripterygium
- From: National Journal of Andrology 2016;22(9):827-833
- CountryChina
- Language:Chinese
-
Abstract:
ObjectiveTo investigate the protective effect of Wuziyanzong Pills (WYP) in the rat model of oligoasthenospermia (OAS) and its action mechanism.
METHODSSixty 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.
RESULTSWYP 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.
CONCLUSIONSWYP 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.