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An anti-αVß3 antibody inhibits coronary artery atherosclerosis in diabetic pigs.
Maile, L A; Busby, W H; Xi, G; Gollahan, K P; Flowers, W; Gafbacik, N; Gafbacik, S; Stewart, K; Merricks, E P; Nichols, T C; Bellinger, D A; Clemmons, D R.
Afiliação
  • Maile LA; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Busby WH; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Xi G; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Gollahan KP; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Flowers W; Department of Animal Science, NC State University, Raleigh, NC, USA.
  • Gafbacik N; Department of Animal Science, NC State University, Raleigh, NC, USA.
  • Gafbacik S; Department of Animal Science, NC State University, Raleigh, NC, USA.
  • Stewart K; Department of Animal Science, NC State University, Raleigh, NC, USA.
  • Merricks EP; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Nichols TC; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Bellinger DA; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.
  • Clemmons DR; Department of Medicine, UNC School of Medicine, Chapel Hill, NC, USA. Electronic address: endo@med.unc.edu.
Atherosclerosis ; 258: 40-50, 2017 03.
Article em En | MEDLINE | ID: mdl-28189040
ABSTRACT
BACKGROUND AND

AIMS:

Diabetes is a major risk factor for the development of atherosclerosis. Hyperglycemia stimulates vascular smooth muscle cells (VSMC) to secrete ligands that bind to the αVß3 integrin, a receptor that regulates VSMC proliferation and migration. This study determined whether an antibody that had previously been shown to block αVß3 activation and to inhibit VSMC proliferation and migration in vitro, inhibited the development of atherosclerosis in diabetic pigs.

METHODS:

Twenty diabetic pigs were maintained on a high fat diet for 22 weeks. Ten received injections of anti-ß3 F(ab)2 and ten received control F(ab)2 for 18 weeks.

RESULTS:

The active antibody group showed reduction of atherosclerosis of 91 ± 9% in the left main, 71 ± 11%, in left anterior descending, 80 ± 10.2% in circumflex, and 76 ± 25% in right coronary artery, (p < 0.01 compared to lesions areas from corresponding control treated arteries). There were significant reductions in both cell number and extracellular matrix. Histologic analysis showed neointimal hyperplasia with macrophage infiltration, calcifications and cholesterol clefts. Antibody treatment significantly reduced number of macrophages contained within lesions, suggesting that this change contributed to the decrease in lesion cellularity. Analysis of the biochemical changes within the femoral arteries that received the active antibody showed a 46 ± 12% (p < 0.05) reduction in the tyrosine phosphorylation of the ß3 subunit of αVß3 and a 40 ± 14% (p < 0.05) reduction in MAP kinase activation.

CONCLUSIONS:

Blocking ligand binding to the αVß3 integrin inhibits its activation and attenuates increased VSMC proliferation that is induced by chronic hyperglycemia. These changes result in significant decreases in atherosclerotic lesion size in the coronary arteries. The results suggest that this approach may have efficacy in treating the proliferative phase of atherosclerosis in patients with diabetes.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Fragmentos Fab das Imunoglobulinas / Integrina alfaVbeta3 / Diabetes Mellitus Experimental / Angiopatias Diabéticas / Músculo Liso Vascular Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Animals Idioma: En Revista: Atherosclerosis Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Doença da Artéria Coronariana / Fragmentos Fab das Imunoglobulinas / Integrina alfaVbeta3 / Diabetes Mellitus Experimental / Angiopatias Diabéticas / Músculo Liso Vascular Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Animals Idioma: En Revista: Atherosclerosis Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos