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[Effect of guanxin no. 2 on gene variant expression profile in rats after myocardial ischemia].

AbstractOBJECTIVE:
To study the effect of Guanxin No. 2 (GX2) on gene variant expression profile in rats after myocardial infarction (MI).
METHODS:
Six SD rats were equally randomized into the sham operated group, the model group and the GX2 group, and they received gastric perfusion with water and GX2 (10 g/kg) respectively. MI model was established by ligating the left-anterior descending branch of coronary artery after 10 days of perfusion, and rats' myocardial tissue in the junction zone was assessed 24 h later for gene chip detection with DNA microarray. Then a cluster analysis was conducted, and the different expressions of key genes were verified by real-time reverse transcription-polymerase chain reaction.
RESULTS:
The up-regulating gene expressions in myocardial tissue in the junction zone increased after ischemia. After GX2 intervention, the up- or down-regulating gene expressions, especially the 2 genes, all-trans-13,14-dihydroretinol saturase (AF465614) and similar to expressed sequence AW413625 (AA799328) decreased significantly. In the common genes, more genes involving activity of signal transducer presented in the model group and the GX2 group and those in the latter showed a certain specificity.
CONCLUSION:
GX2 could improve the characteristics of variant gene expression profile in MI rats to a certain extent.
AuthorsCheng-Yao Yu, Hui-Li Gao, Zhen Liu
JournalZhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine (Zhongguo Zhong Xi Yi Jie He Za Zhi) Vol. 28 Issue 5 Pg. 426-30 (May 2008) ISSN: 1003-5370 [Print] China
PMID18672770 (Publication Type: English Abstract, Journal Article)
Chemical References
  • Drugs, Chinese Herbal
  • guanxin No. 2
  • Oxidoreductases Acting on CH-CH Group Donors
Topics
  • Animals
  • Drugs, Chinese Herbal (pharmacology)
  • Gene Expression (drug effects)
  • Gene Expression Profiling
  • Myocardial Ischemia (genetics, metabolism)
  • Myocardium (metabolism)
  • Oxidoreductases Acting on CH-CH Group Donors (genetics, metabolism)
  • Rats
  • Rats, Sprague-Dawley

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