Adenoviral transfer of HIF-1alpha enhances vascular responses to critical limb ischemia in diabetic mice

Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18769-74. doi: 10.1073/pnas.0910561106. Epub 2009 Oct 19.

Abstract

Diabetes is a major risk factor for ischemic disease. Treatment options for diabetic patients with peripheral arterial disease when revascularization is not possible are limited, resulting in a high incidence of limb amputation. We evaluated the therapeutic potential of AdCA5, an adenovirus encoding a constitutively active form of HIF-1alpha, in a diabetic model of critical limb ischemia. Diabetic db/db and nondiabetic db/+ mice were subjected to unilateral femoral artery ligation. Limb perfusion, tissue viability, and motor function were more severely impaired in db/db mice. Intramuscular injection of AdCA5 into the ischemic limb of db/db mice increased the recovery of limb perfusion and function, reduced tissue necrosis, rescued the diabetes-associated impairment of circulating angiogenic cells, enhanced endothelial nitric oxide synthase activation, and increased vessel density and luminal area in the ischemic limb.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Animals
  • Diabetes Mellitus, Experimental / complications*
  • Diabetes Mellitus, Experimental / enzymology
  • Diabetes Mellitus, Experimental / pathology
  • Extremities / blood supply*
  • Extremities / pathology
  • Femoral Artery / surgery
  • Genetic Therapy*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Hypoxia-Inducible Factor 1, alpha Subunit / therapeutic use*
  • Immunohistochemistry
  • Ischemia / complications
  • Ischemia / enzymology
  • Ischemia / pathology
  • Ischemia / therapy*
  • Ligation
  • Mice
  • Muscle, Skeletal / enzymology
  • Muscle, Skeletal / pathology
  • Neovascularization, Physiologic
  • Nitric Oxide Synthase Type III / metabolism
  • Signal Transduction

Substances

  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Nitric Oxide Synthase Type III