Effects of treatment with Astragalus Membranaceus on function of rat leydig cells

被引:17
作者
Jiang, Xiaolong [1 ]
Cao, Xia [1 ]
Huang, Yang [1 ]
Chen, Jianwei [1 ]
Yao, Xiaolei [1 ]
Zhao, Miaomiao [1 ]
Liu, Yan [1 ]
Meng, Jinzhu [1 ]
Li, Pengfei [2 ]
Li, Zhiyan [3 ]
Yao, Jianbo [1 ,7 ]
Smith, George W. [1 ,4 ,5 ,6 ]
Lv, Lihua [1 ]
机构
[1] Shanxi Agr Univ, Coll Anim Sci & Technol, Taigu 030801, Peoples R China
[2] Shanxi Agr Univ, Coll Life Sci, Taigu 030801, Shanxi, Peoples R China
[3] Fudan Univ, Pharmaceut Anal Lab, Shanghai 200000, Peoples R China
[4] Michigan State Univ, Lab Mammalian Reprod Biol & Genom, E Lansing, MI 48824 USA
[5] Michigan State Univ, Dept Anim Sci, E Lansing, MI 48824 USA
[6] Michigan State Univ, Dept Anim Physiol, E Lansing, MI 48824 USA
[7] W Virginia Univ, Div Anim & Nutr Sci, Morgantown, WV 26506 USA
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2015年 / 15卷
关键词
Astragalus membranaceus; Leydig cell; SOD and GPx; Bax; Bcl-2; Testosterone; INDUCED DIABETIC-RATS; NF-KAPPA-B; STEM-CELLS; IN-VITRO; IV; INJURY; APOPTOSIS; ISCHEMIA; PATHWAY; VIVO;
D O I
10.1186/s12906-015-0776-3
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Astragalus membranaceus (AM) is a Chinese traditional herb which has been reported to have broad positive effects on many diseases, including hepatitis, heart disease, diabetes and skin disease. AM can promote cell proliferation, increase the activities of superoxide dismutase (SOD) and glutathione peroxidase (GPx), and inhibit apoptosis by regulating the transcription of proto-oncogenes controlling cell death. While AM is included in some commercially available "testosterone boosting supplements", studies directly testing ability of AM to modulate testosterone production are lacking. In the present study, we examined the effects of AM on Leydig cell function in vitro. Methods: Rat Leydig cells were purified and treated with AM at different concentrations (0 mu g/mL, 10 mu g/mL, 20 mu g/mL, 50 mu g/mL, 100 mu g/mL and 150 mu g/mL) and cell counting-8 (CCK-8) assay, Enzyme-linked immunosorbent assay, quantitative real time PCR and analysis of activities of SOD and GPx were done respectively. Results: Treatment with 100 mu g/mL (P < 0.05) and 150 mu g/mL AM (P < 0.01) significantly increased Leydig cell numbers. Treatment with AM (20 mu g/mL, 50 mu g/mL and 100 mu g/mL) significantly increased testosterone production (P < 0.01). In addition, increased Leydig cell SOD and GPx activities were observed in response to 20 mu g/mL and 50 mu g/mL AM treatment (P < 0.01). Furthermore, expression of Bax mRNA was significantly decreased (P < 0.01), and the ratio of Bcl-2/Bax mRNA was significantly increased in response to 20 mu g/mL AM in the culture medium (P < 0.05). Conclusions: Results supported a beneficial effect of AM on multiple aspects of rat Leydig cell function in vitro including testosterone production.
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页数:6
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