[Effects of varglaucocalyx on c-fos gene expression during global myocardial ischemia-reperfusion in rat]

Zhongguo Zhong Yao Za Zhi. 2003 Apr;28(4):358-61.
[Article in Chinese]

Abstract

Objective: To determine the effects of Varglaucocalyx on c-fos gene expression during global myocardial ischemia-reperfusion.

Method: Forty Wistar rats were divided into 5 groups: group N as control; group CN as ischemia-reperfusion control and group XH, XM and XL treated with Varglaucocalyx 5%, 1%, 0.5% respectively prior to ischemia-reperfusion. The isolated rat hearts were perfused in condition of constant temperature and pressure, and then the left ventricular myocardiums were extracted for use. The expression of c-fos protein was detected by immunochemical method. The expression of c-fos protein were quantified by using computer image analysis system.

Result: Compared with the values of group N, protein expressions relative area of c-fos gene (PERA) were increased significantly in group CN, XH, XM, XL(P < 0.01), but decreased significantly in group XH, XM, XL, compared with those of group CN (P < 0.05). The PERA of c-fos gene in group XM, XL were significantly lower than in group XH (P < 0.01), and the PERA of c-fos gene in group XM were lower than in group XL(P < 0.05).

Conclusion: Varglaucocalyx can effectively depress the expression of c-fos gene in myocardium which may account for its protection against myocardial ischemia-reperfusion injury, and the middle and the low concentrations of Varglaucocalyx are more effective than the high concentrations.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiotonic Agents / pharmacology
  • Drugs, Chinese Herbal / isolation & purification
  • Drugs, Chinese Herbal / pharmacology*
  • Female
  • Gene Expression Regulation / drug effects
  • Genes, fos*
  • Isodon* / chemistry
  • Male
  • Myocardial Reperfusion Injury / etiology
  • Myocardial Reperfusion Injury / metabolism*
  • Myocardium / metabolism
  • Plants, Medicinal / chemistry
  • Proto-Oncogene Proteins c-fos / biosynthesis*
  • Random Allocation
  • Rats
  • Rats, Wistar

Substances

  • Cardiotonic Agents
  • Drugs, Chinese Herbal
  • Proto-Oncogene Proteins c-fos