Key result
Daily adiponectin replacement in leptin-deficient mice inhibited the development of severe viral myocarditis by augmenting myocyte adiponectin receptor 1 reactivity.
Why the study?
Does adiponectin replacement therapy attenuate myocardial damage in leptin-deficient mice with viral myocarditis?
Does adiponectin replacement therapy attenuate myocardial damage in leptin-deficient mice with viral myocarditis?
Exogenously administered adiponectin may inhibit the progression of viral myocarditis in leptin-deficient conditions by binding to adiponectin receptor 1.
Answers are grounded in this paper and cite their sources.
Adiponectin replacement merits further study in leptin-deficient viral myocarditis models; hypothesis-generating and should not change practice.
The effects of adiponectin replacement therapy on myocardial damage were studied in leptin-deficient (OB) mice with acute viral myocarditis. Encephalomyocarditis virus was injected intraperitoneally into OB and wild-type (WT) mice. One subgroup of OB mice received no intervention and another subgroup received daily adiponectin replacement, simultaneously with viral inoculation. Differences in heart weight, cardiac histological score, numbers of infiltrating or apoptotic cells in the myocardium and the immunoreactivity of adiponectin receptors in myocytes were determined. The reactivity of adiponectin receptor 1 in myocytes from OB mice on day 4 and day 8 after viral inoculation was significantly decreased compared with that in myocytes from WT mice; the OB mice also had elevated cardiac weights and severe inflammatory myocardial damage. Adiponectin replacement in OB mice inhibited the development of severe myocarditis by augmenting myocyte adiponectin receptor 1 reactivity. Exogenously administered adiponectin may inhibit the progression of viral myocarditis through binding to the adiponectin receptor 1 in leptin-deficient conditions.
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Takahashi et al. (2005) studied Acute viral myocarditis. Adiponectin replacement therapy vs. No intervention was evaluated on Myocardial damage (heart weight, histological score, infiltrating/apoptotic cells, adiponectin receptor immunoreactivity). Daily adiponectin replacement in leptin-deficient mice inhibited the development of severe viral myocarditis by augmenting myocyte adiponectin receptor 1 reactivity.
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