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PMID: 15249181 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Differences in atrial versus ventricular remodeling in dogs with ventricular tachypacing-induced congestive heart failure.

Cardiovascular research ·Vol. 63 ·No. 2 ·2004-08-01 ·Pages 236-44

Hanna N, Cardin S, Leung TK, Nattel S

Abstract

Congestive heart failure (CHF) causes arrhythmogenic remodeling in both atria and ventricles, but differences between atrial and ventricular remodeling in CHF have not been well characterized. We examined atrial and ventricular tissues from dogs with CHF induced by ventricular tachypacing (220-240/min) for 0 (control) or 24 h, or 1, 2 or 5 weeks. Histopathology was used to assess apoptosis, fibrosis, white blood cell infiltration and cell death, ELISA to measure angiotensin-II concentration and Western blot to evaluate protein expression. Ventricular tachypacing-induced CHF was associated with substantially more fibrosis in left atrium (maximum 10 +/- 1% at 5 weeks) than in left ventricle (0.4 +/- 0.1% at 5 weeks, P < 0.01 versus left atrium). Tissue angiotensin-II concentration increased to steady state in atrial tissue at 24 h but increased more slowly in left ventricle, with a maximum that was significantly higher in atrium than ventricle. Ventricular tachypacing caused tissue apoptosis, inflammatory cell infiltration and cell death, with maximum changes in left atrium being faster, transient and larger than in left ventricle. Mitogen activated protein kinase activation was rapid (within 24 h) in left atrium, but smaller and slower (p38, c-Jun N-terminal kinase) or non-significant (extracellular signal-related kinase) in left ventricle. The 25-kDa activated form of transforming growth factor-beta1, a particularly important profibrotic mediator in atrium, increased significantly in left atrium, from 2.6 +/- 0.6 (control) to 9.2 +/- 1.7 (24 h) and 8.1 +/- 1.8 optical density units (1 week), but was not significantly changed in ventricle. There are qualitative and quantitative differences in atrial versus ventricular remodeling in experimental ventricular tachypacing-induced CHF, with potentially important consequences for understanding underlying mechanisms and developing new therapeutic approaches.

MeSH Terms
Angiotensin II/analysis Animals Apoptosis Blotting, Western/methods Cardiac Pacing, Artificial Cell Death Dogs Fibrosis Heart Atria/metabolism,pathology Heart Failure/metabolism,pathology,physiopathology Heart Ventricles/metabolism,pathology Humans Leukocytes/pathology Mitogen-Activated Protein Kinases/analysis,metabolism Transforming Growth Factor beta/analysis Ventricular Remodeling
Chemicals
Transforming Growth Factor beta Angiotensin II Mitogen-Activated Protein Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hanna Nessrine
Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec, Canada.
Cardin Sophie
Leung Tack-Ki
Nattel Stanley
Article Info
Journal
Cardiovascular research
Abbr.
Cardiovasc Res
ISSN
0008-6363
Published
2004-08-01
Pages
236-44
Language
English
Region
England
NLM ID
0077427
Subset
IM
Corrections
CommentIn
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