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  • 标题:Effects of Metformin on Rosiglitazone-Induced Cardiac Hypertrophy in Mice
  • 本地全文:下载
  • 作者:Hsiu-Hao Lee ; Ching-Hua Yeh ; Yu-Tai Chen
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2010
  • 卷号:33
  • 期号:9
  • 页码:1506-1510
  • DOI:10.1248/bpb.33.1506
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Thiazolidinediones (TZD) can cause adipose tissue accumulation and myocardial hypertrophy. This study aimed to determine if combined Metformin (Glucophage) and Rosiglitazone (Avandia) could reduce the risk of heart failure caused by Rosiglitazone in BALB/c mice. BALB/c mice were treated with oral Rosiglitazone/Metformin twice daily for four weeks. Metformin or Rosiglitazone alone and non-treated mice acted as double control. Myocardial hypertrophy and associated side effects of the combined therapy were determined through isolated heart and body weights. Reverse transcription-polymerase chain reaction (RT-PCR) and Western blot were applied to evaluate expression of sulfonylurea receptor 2A (SUR2A) and Kir 6.2. The activities of peroxisome proliferator activated receptor α (PPARα) in the myocardium were also observed. Rosiglitazone/Metformin decreased body weight gain and food intake, and inhibited an increasing adipose ratio but did not reduce myocardial hypertrophy. Rosiglitazone increased Kir6.2/SUR2A, Kir6.2/SUR2B, and PPARα gene expression. The Rosiglitazone/Metformin combination further increased these gene expressions, especially PPARα. Metformin inhibits obesity but has no effect in reducing myocardial hypertrophy caused by Rosiglitazone. Whether Metformin can reduce side effects of TZDs in humans warrants further study.
  • 关键词:Metformin;Rosiglitazone;myocardial hypertrophy;obesity;adipose accumulation
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