Effect of heparin treatment on the expression and activity of different ion-motive P-type ATPase isoforms from mouse extensor digitorum longus muscle during degeneration and regeneration after Bothrops jararacussu venom injection

Toxicon. 2010 Jan;55(1):52-60. doi: 10.1016/j.toxicon.2009.06.032. Epub 2009 Jul 3.

Abstract

Ca(2+) ions are essential to myonecrosis, a serious complication of snake envenomation, and heparin seems to counteract this effect. We investigated the effect of local injection of Bothrops jararacussu venom in mouse fast-twitch extensor digitorum longus (EDL) muscle, without or with heparin, on functional/molecular alterations of two central proteins involved in intracellular Ca(2+) homeostasis, sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA) and Na(+)/K(+)-ATPase. EDL-specific SERCA1 isoform expression dropped significantly just after venom administration (up to 60% compared to control EDL values at days 1 and 3; p<0.05) while SERCA2 and Na(+)/K(+)-ATPase alpha(1) isoform expression increased at the same time (3-6- and 2-3-fold, respectively; p<0.05). Although not significant, Na(+)/K(+)-ATPase alpha(2) isoform followed the same trend. Except for SERCA2, all proteins reached basal levels at the 7th day. Intravenous heparin treatment did not affect these profiles. Ca(2+)-ATPase activity was also decreased during the first days after venom injection, but here heparin was effective to reinstate activity to control levels within 3 days. We also showed that B. jararacussu venom directly inhibited Ca(2+)-ATPase activity in a concentration-dependent manner. Our results indicate that EDL SERCA and Na(+)/K(+)-ATPase are importantly affected by B. jararacussu venom and heparin has protective effect on activity but not on protein expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Antivenins / pharmacology*
  • Bothrops
  • Crotalid Venoms / toxicity*
  • Dose-Response Relationship, Drug
  • Female
  • Heparin / pharmacology*
  • Isoenzymes / metabolism
  • Male
  • Mice
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Necrosis / chemically induced
  • Organ Specificity
  • Rats
  • Rats, Wistar
  • Regeneration / drug effects*
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism*
  • Species Specificity
  • Time Factors

Substances

  • Antivenins
  • Crotalid Venoms
  • Isoenzymes
  • Heparin
  • Adenosine Triphosphatases
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases