Journal
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
Volume 23, Issue 4-6, Pages 327-334Publisher
KARGER
DOI: 10.1159/000218180
Keywords
Interleukins; Extracellular matrix; Hypertrophy; Remodeling
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Funding
- Deutsche Forschungsgemeinschaft [ZI 199/10-4]
- Medical Faculty of the University of Leipzig [1-10]
- BMBF [01ZZ01106]
- Ernst von Weber foundation
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Background: Elevated serum concentration of interleukin (IL)-6 is a predictor for poor prognosis in congestive heart failure. It was shown previously in rats, that IL-6 expression in the left ventricle (LV) was followed by LV hypertrophy. Methods: Using IL-6 deficient mice (IL-6(-/-)), we studied the role of IL-6 in a model of norepinephrine (NE)-induced LV hypertrophy. Results: In wild type (WT) mice, IL-6 mRNA expression and its concentration in the serum were elevated after 4 h of NE-treatment (s.c. 0.25 mg/kg . h). Further, NE-induced LV hypertrophy was detected: LV weight/body weight (LVW/BW) ratio (+ 12.3 +/- 3%, p < 0.05) and mRNA expression of atrial natriuretic peptide (ANP) in WT mice (+ 120 +/- 25%, p < 0.05) after 3 days were increased. In contrast, NE did not induce elevation of LVW/BW ratio and ANP expression in IL-6(-/-) mice. Replacement with recombinant IL-6 restored the hypertrophy-inducing effect of NE in IL-6(-/-) mice. As to the extracellular matrix (ECM) proteins, NE increased collagen type I and III expression only in WT mice and not in IL-6(-/-) mice. The addition of recombinant IL-6 elevated the expression of the ECM proteins to the WT level. Conclusion: IL-6 is a major player in the development of NE-induced LV hypertrophy in mice. Copyright (C) 2009 S. Karger AG, Basel
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