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Prevention of Osteopenia and Dyslipidemia in Rats after Ovariectomy with Combined Aspirin and Low-dose Diethylstilbestrol

Prevention of Osteopenia and Dyslipidemia in Rats after Ovariectomy with Combined Aspirin and Low-dose Diethylstilbestrol

作     者:LIN Si En HUANG Jian Ping WU Ling Zhi WU Tie CUI Liao 

作者机构:Department of PharmacologyGuangdong Medical College Department of StomatologyGuangdong Medical College Guangdong Key Laboratory for Research and Development of Natural Drugs 

出 版 物:《Biomedical and Environmental Sciences》 (生物医学与环境科学(英文版))

年 卷 期:2013年第26卷第4期

页      面:249-257页

核心收录:

学科分类:1006[医学-中西医结合] 0830[工学-环境科学与工程(可授工学、理学、农学学位)] 1004[医学-公共卫生与预防医学(可授医学、理学学位)] 1001[医学-基础医学(可授医学、理学学位)] 10[医学] 100602[医学-中西医结合临床] 

基  金:supported by grants from the National Science Foundation of China (No:30973574) Science and Technology Planning Project of Guangdong Province (No:2010B060500014) Science & Technology Innovation Fund of Guangdong Medical College (STIF201104) 

主  题:Aspirin Diethylstilbestrol Ovariectomy Osteoporosis Dyslipidemia Rat 

摘      要:Objective To study whether effect of aspirin plus low-dose diethylstilbestrol is more effective and safer than high diethylstilbestrol dose alone on prevention of ovariectomy-induced osteopenia and dyslipidemia. Methods Thirty-eight 4-month-old female SD rats were divided into baseline (BAS) group (n=6), sham operation group (n=8) and ovariectomy (OVX) group (n=24). The OVX group was further divided into vehicle treatment group (n=8), diethylstilbestrol (30 ug/kg.d) treatment group (OVX+D30 group, n=8), and aspirin (9 mg/kg.d) plus diethylstilbestrol (10 ug/kg.d) treatment group (OVX+A-D10 group, n=8). Their left tibiae were collected for the bone histomorphometric analysis in undecalcified sections. Left femurs were collected for the bone mineral density measurement. Results The body weight and serum cholesterol were increased, while uterine weight and cancellous bone mass were decreased in OVX rats compared with the SHAM group. Cancellous bone mass was significantly increased, while body weight and bone resorption parameters were decreased in both A-D10 and D30 treatment group compared with OVX group. The rats treated with A-D10 showed significantly increased in bone formation parameters and decreased in serum triglyceride compared with the D30-treated rats. Conclusion Aspirin plus low-dose diethylstilbestrol can effectively prevent osteopenia by reducing bone resorption, and is thus a better treatment modality for preventing dyslipidemia than high-dose diethylstilbestrol alone.

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