Extracellular signal-regulated kinase 1/2 activation is involved in intermedin1-53 attenuating myocardial oxidative stress injury induced by ischemia/reperfusion

Peptides. 2012 Feb;33(2):329-35. doi: 10.1016/j.peptides.2011.12.016. Epub 2012 Jan 8.

Abstract

Intermedin (IMD)(1-53) is a novel member of the calcitonin gene-related peptide superfamily and has potent cardioprotective effects against myocardial injury induced by ischemia-reperfusion (I/R). To explore the mechanism of the IMD(1-53) cardioprotective effect, we studied the anti-oxidant effects of IMD(1-53) on myocardial injury induced by I/R in vivo in rat and H(2)O(2) treatment in vitro in rat cardiomyocytes. Compared with sham treatment, I/R treatment induced severe lipid peroxidation injury in rat myocardium: plasma malondialdehyde (MDA) content and myocardial LDH activity was increased by 34% and 85% (all P<0.01); Mn-superoxide dismutase (Mn-SOD) and catalase (CAT) activity was reduced 80% and 86% (all P<0.01), respectively, and the protein levels of the NADPH oxidase complex subunits gp91(phox) and p47(phox) were markedly increased, by 86% (P<0.05) and 95% (P<0.01), respectively; IMD(1-53) treatment ameliorated lipid peroxidation injury: plasma MDA content and myocardial LDH activity was decreased by 30% (P<0.05) and 36% (P<0.01); Mn-SOD and CAT activity was elevated 1.0- and 4.3-fold (all P<0.01), respectively; and the protein levels of gp91(phox) and p47(phox) were reduced, by 28% and 36% (both P<0.05), respectively. Concurrently, IMD(1-53) treatment markedly promoted cell viability and inhibited apoptosis in cardiomyocytes as compared with H(2)O(2) treatment alone. Furthermore, IMD(1-53) increased the ratio of p-ERK to ERK by 66% (P<0.05) as compared with I/R alone, and the protective effect of IMD(1-53) on H(2)O(2)-induced apoptosis was abolished by preincubation with PD98059, a MEK inhibitor. IMD(1-53) may improve the oxidative stress injury induced by I/R via inhibiting the production of reactive oxygen species and enhancing ERK phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenomedullin / metabolism
  • Adrenomedullin / physiology*
  • Animals
  • Antioxidants / metabolism
  • Antioxidants / physiology*
  • Caspase 3 / metabolism
  • Catalase / metabolism
  • Cell Survival
  • Cells, Cultured
  • Cytoprotection
  • Enzyme Activation
  • Hydrogen Peroxide / pharmacology
  • L-Lactate Dehydrogenase / metabolism
  • MAP Kinase Signaling System*
  • Male
  • Malondialdehyde / blood
  • Membrane Glycoproteins / metabolism
  • Myocardial Ischemia / enzymology
  • Myocardial Ischemia / metabolism*
  • Myocardial Reperfusion Injury / enzymology
  • Myocardial Reperfusion Injury / metabolism*
  • Myocardium / enzymology
  • Myocardium / metabolism
  • Myocardium / pathology
  • Myocytes, Cardiac / drug effects
  • Myocytes, Cardiac / metabolism
  • Myocytes, Cardiac / physiology
  • NADPH Oxidase 2
  • NADPH Oxidases / metabolism
  • Neuropeptides / metabolism
  • Neuropeptides / physiology*
  • Oxidants / pharmacology
  • Oxidative Stress*
  • Peptide Fragments / physiology
  • Protein Isoforms / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / metabolism

Substances

  • Adm2 protein, rat
  • Antioxidants
  • Membrane Glycoproteins
  • Neuropeptides
  • Oxidants
  • Peptide Fragments
  • Protein Isoforms
  • Adrenomedullin
  • Malondialdehyde
  • Hydrogen Peroxide
  • L-Lactate Dehydrogenase
  • Catalase
  • Superoxide Dismutase
  • Cybb protein, rat
  • NADPH Oxidase 2
  • NADPH Oxidases
  • neutrophil cytosolic factor 1
  • Casp3 protein, rat
  • Caspase 3