Polynitroxyl alphaalpha-hemoglobin (PNH) inhibits peroxide and superoxide-mediated neutrophil adherence to human endothelial cells

Free Radic Res. 1999 Jul;31(1):53-8. doi: 10.1080/10715769900300591.

Abstract

Experimental hemoglobin-based O2 carriers e.g. cross-linked alphaalpha-hemoglobin (alphaalpha-Hb), are under investigation as potential blood substitutes. However, some Hb-based products form strong oxidant species in vivo that may cause adverse clinical effects. We report the prototype of a new class of modified Hb-based O2 carrier, polynitroxylated alphaalpha-Hb (PNH), which has antioxidant activities that may reduce inflammatory effects mediated by oxidant formation. We compared the effects of alphaalpha-Hb and PNH on xanthine oxidase and H2O2-induced neutrophil-endothelial adhesion in vitro. Both peroxide (>0.1 mM), and superoxide/peroxide generated by xanthine oxidase (XO) (> 10 mU/ml) + 0.1 mM xanthine (X), increased endothelial-neutrophil adhesion. At 30 microM, alphaalpha-Hb significantly increased X/XO-mediated adhesion, while PNH inhibited peroxide or X/XO induced adhesion, with maximal inhibition at 10 microM PNH. These data indicate that PNH has antioxidant-anti-inflammatory properties that suggest its use as a potentially safer blood substitute in reperfusion injury, stroke, myocardial infarction and other forms of inflammation.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Antioxidants / pharmacology
  • Blood Substitutes / pharmacology*
  • Cell Adhesion / drug effects*
  • Cells, Cultured
  • Endothelium, Vascular / cytology*
  • Hemoglobins / pharmacology*
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Neutrophils / physiology*
  • Nitrogen Oxides / pharmacology*
  • Superoxides / pharmacology*
  • Umbilical Veins
  • Xanthine / pharmacology
  • Xanthine Oxidase / pharmacology

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • Blood Substitutes
  • Hemoglobins
  • Nitrogen Oxides
  • polynitroxyl hemoglobin
  • Superoxides
  • Xanthine
  • Hydrogen Peroxide
  • Xanthine Oxidase