Cardioprotective effect of paeonol and danshensu combination on isoproterenol-induced myocardial injury in rats

PLoS One. 2012;7(11):e48872. doi: 10.1371/journal.pone.0048872. Epub 2012 Nov 6.

Abstract

Background: Traditional Chinese medicinal herbs Cortex Moutan and Radix Salviae Milthiorrhizaeare are prescribed together for their putative cardioprotective effects in clinical practice. However, the rationale of the combined use remains unclear. The present study was designed to investigate the cardioprotective effects of paeonol and danshensu (representative active ingredient of Cortex Moutan and Radix Salviae Milthiorrhizae, respectively) on isoproterenol-induced myocardial infarction in rats and its underlying mechanisms.

Methodology: Paeonol (80 mg kg(-1)) and danshensu (160 mg kg(-1)) were administered orally to Sprague Dawley rats in individual or in combination for 21 days. At the end of this period, rats were administered isoproterenol (85 mg kg(-1)) subcutaneously to induce myocardial injury. After induction, rats were anaesthetized with pentobarbital sodium (35 mg kg(-1)) to record electrocardiogram, then sacrificed and biochemical assays of the heart tissues were performed.

Principal findings: Induction of rats with isoproterenol resulted in a marked (P<0.001) elevation in ST-segment, infarct size, level of serum marker enzymes (CK-MB, LDH, AST and ALT), cTnI, TBARS, protein expression of Bax and Caspase-3 and a significant decrease in the activities of endogenous antioxidants (SOD, CAT, GPx, GR, and GST) and protein expression of Bcl-2. Pretreatment with paeonol and danshensu combination showed a significant (P<0.001) decrease in ST-segment elevation, infarct size, cTnI, TBARS, protein expression of Bax and Caspase-3 and a significant increase in the activities of endogenous antioxidants and protein expression of Bcl-2 and Nrf2 when compared with individual treated groups.

Conclusions/significance: This study demonstrates the cardioprotective effect of paeonol and danshensu combination on isoproterenol-induced myocardial infarction in rats. The mechanism might be associated with the enhancement of antioxidant defense system through activating of Nrf2 signaling and anti-apoptosis through regulating Bax, Bcl-2 and Caspase-3. It could provide experimental evidence to support the rationality of combinatorial use of traditional Chinese medicine in clinical practice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetophenones / chemistry
  • Acetophenones / pharmacology
  • Acetophenones / therapeutic use*
  • Animals
  • Antioxidants / metabolism
  • Biomarkers / blood
  • Body Weight / drug effects
  • Cardiotonic Agents / chemistry
  • Cardiotonic Agents / pharmacology
  • Cardiotonic Agents / therapeutic use*
  • Caspase 3 / metabolism
  • Drug Therapy, Combination
  • Electrocardiography
  • Glutathione / metabolism
  • Immunohistochemistry
  • Isoproterenol
  • Lactates / chemistry
  • Lactates / pharmacology
  • Lactates / therapeutic use*
  • Lipid Peroxidation / drug effects
  • Male
  • Myocardial Infarction / blood
  • Myocardial Infarction / diagnostic imaging
  • Myocardial Infarction / drug therapy*
  • Myocardial Infarction / pathology*
  • Myocardium / enzymology
  • Myocardium / pathology*
  • NF-E2-Related Factor 2 / metabolism
  • Organ Size / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Troponin I / metabolism
  • Ultrasonography
  • bcl-2-Associated X Protein / metabolism

Substances

  • Acetophenones
  • Antioxidants
  • Biomarkers
  • Cardiotonic Agents
  • Lactates
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Thiobarbituric Acid Reactive Substances
  • Troponin I
  • bcl-2-Associated X Protein
  • paeonol
  • 3,4-dihydroxyphenyllactic acid
  • Caspase 3
  • Glutathione
  • Isoproterenol

Grants and funding

Funding for this study was provided in part by research grants S2010ZDGC105 and 2011K12-53 from Shaanxi Province, the People's Republic of China. No additional external funding was received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.