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Anti-apoptotic and uterotrophic effects of Heyan Kuntai capsules in uterus of ovariectomized rats
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DOI   10.11656/j.issn.1672-1519.2016.11.11
Key Words   Heyan Kuntai capsule;uterus morphology;apoptosis;Bcl-2 mRNA and protein;Bax mRNA and protein
Author NameAffiliationE-mail
HUANG Chun-li Traditional Chinese Medicine Research Institute of Tianjin University of Triditional Chinese Medicine, Tianjin 300193, China  
ZHANG De-qin Traditional Chinese Medicine Research Institute of Tianjin University of Triditional Chinese Medicine, Tianjin 300193, China deqin123@163.com 
ZHANG Qing-xia Traditional Chinese Medicine Research Institute of Tianjin University of Triditional Chinese Medicine, Tianjin 300193, China  
WEN Jing Traditional Chinese Medicine Research Institute of Tianjin University of Triditional Chinese Medicine, Tianjin 300193, China  
Abstract
    [Objective] To investigate the effects of Heyan Kuntai capsules on uterus morphology and apoptosis in ovariectomized rats.[Methods] Female SD rats underwent ovariectomize surgery and were divided into model group, progynova group, Remifemin group and Heyan Kuntai capsule of high, medium and low dose groups (8, 4 and 2 g crude drug/kg respectively). The drugs were administered for 8 weeks. This article observed the impacts of drugs on uterus pathology, staining and apoptosis, detected the expression levels of Bcl-2 and Bax mRNAs and proteins.[Results] It was obtained significantly decreased epithelial thickness and reduced myometrium and endometrium cross-sectional area and wall thickness in the model group compared with the control and Heyan Kuntai capsule treated groups(P<0.01 or P<0.05). It was also decreased Bcl-2 and increased Bax mRNAs and proteins expressions(P<0.01 or P<0.05) in the model group. Further more, the model group showed increased apoptosis rate(P<0.01 or P<0.05) and reduced number of glands(P<0.01 or P<0.05) in the uterus.[Conclusion] Heyan Kuntai capsules elicits uterotrophic effect and attenuates apoptosis in the uterus cells by regulating mRNAs and protein expressions of Bcl-2 and Bax.

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