3.9 Article

Alpha-calcitonin gene-related peptide is protective against pressure overload-induced heart failure

Journal

REGULATORY PEPTIDES
Volume 185, Issue -, Pages 20-28

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.regpep.2013.06.008

Keywords

Sensory nervous system; Neuropeptides; Cardiac hypertrophy; Inflammation; Heart failure

Funding

  1. University of South Carolina
  2. National Institutes of Health [R00HL093215]

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The sensory neuropeptide, alpha-calcitonin gene-related peptide (alpha-CGRP) is protective against hypertension-induced heart damage and cardiac ischemia/reperfusion injury. To determine whether this neuropeptide is also cardioprotective in heart failure, this study examined whether the absence of alpha-CGRP exacerbated the adverse cardiac remodeling, dysfunction and mortality in pressure overload heart failure induced by transverse aortic constriction (TAC). Male alpha-CGRP knockout (1(0) and wild type (WT) mice had TAC or sham surgery at day 0 and were studied on days 3, 14, 21, and 28. The survival rate of TAC alpha-CGRP KO mice was lower than the TAC WT mice over the duration of the protocol. Left ventricular alpha-CGRP content in TAC WT mice was higher at days 3, 14, and 21 than sham WT mice. Echocardiography demonstrated greater adverse cardiac remodeling and dysfunction in the TAC alpha-CGRP KO compared to the TAC WT mice. The lung/body weight ratios and left ventricular masses were higher in TAC alpha-CGRP KO compared to the TAC WT mice. While there was increased cardiac fibrosis in the TAC WT mice compared to shams, the TAC alpha-CGRP KO mice had markedly increased fibrosis above that of the TAC WT mice. TAC WT mice had greater cardiac inflammation, cell death, and adaptive angiogenesis compared to sham mice. Importantly, the TAC alpha-CGRP KO mice had greater inflammation, cell death, and attenuation of angiogenesis compared to TAC WT hearts. Thus, alpha-CGRP plays a significant protective role in TAC-induced heart failure which may be mediated by decreased inflammation, cell death, and fibrosis. (C) 2013 Elsevier B.V. All rights reserved.

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