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The brighter (and evolutionarily older) face of the metabolic syndrome: evidence from Trypanosoma cruzi infection in CD-1 mice
W. Brima, DJ. Eden, SF. Mehdi, M. Bravo, MM. Wiese, J. Stein, V. Almonte, D. Zhao, I. Kurland, JE. Pessin, T. Zima, HB. Tanowitz, LM. Weiss, J. Roth, F. Nagajyothi,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu srovnávací studie, časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
PubMed
25613819
DOI
10.1002/dmrr.2636
Knihovny.cz E-zdroje
- MeSH
- adipozita účinky léků MeSH
- analýza přežití MeSH
- bílá tuková tkáň účinky léků imunologie metabolismus parazitologie MeSH
- buněčné linie MeSH
- Chagasova nemoc krev imunologie metabolismus parazitologie MeSH
- cytokiny krev metabolismus MeSH
- energetický metabolismus účinky léků MeSH
- hypoglykemika farmakologie terapeutické užití MeSH
- inbrední kmeny myší MeSH
- leptin krev metabolismus MeSH
- lidé MeSH
- metabolický syndrom farmakoterapie etiologie imunologie parazitologie MeSH
- metformin farmakologie terapeutické užití MeSH
- modely imunologické * MeSH
- náhodné rozdělení MeSH
- obezita krev imunologie metabolismus patofyziologie MeSH
- předkožka účinky léků imunologie metabolismus parazitologie MeSH
- srdeční komory účinky léků imunologie metabolismus parazitologie MeSH
- Trypanosoma cruzi účinky léků imunologie izolace a purifikace patogenita MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- srovnávací studie MeSH
BACKGROUND: Infection with Trypanosoma cruzi, the protozoan parasite that causes Chagas disease, results in chronic infection that leads to cardiomyopathy with increased mortality and morbidity in endemic regions. In a companion study, our group found that a high-fat diet (HFD) protected mice from T. cruzi-induced myocardial damage and significantly reduced post-infection mortality during acute T. cruzi infection. METHODS: In the present study metabolic syndrome was induced prior to T. cruzi infection by feeding a high fat diet. Also, mice were treated with anti-diabetic drug metformin. RESULTS: In the present study, the lethality of T. cruzi (Brazil strain) infection in CD-1 mice was reduced from 55% to 20% by an 8-week pre-feeding of an HFD to induce obesity and metabolic syndrome. The addition of metformin reduced mortality to 3%. CONCLUSIONS: It is an interesting observation that both the high fat diet and the metformin, which are known to differentially attenuate host metabolism, effectively modified mortality in T. cruzi-infected mice. In humans, the metabolic syndrome, as presently construed, produces immune activation and metabolic alterations that promote complications of obesity and diseases of later life, such as myocardial infarction, stroke, diabetes, Alzheimer's disease and cancer. Using an evolutionary approach, we hypothesized that for millions of years, the channeling of host resources into immune defences starting early in life ameliorated the effects of infectious diseases, especially chronic infections, such as tuberculosis and Chagas disease. In economically developed countries in recent times, with control of the common devastating infections, epidemic obesity and lengthening of lifespan, the dwindling benefits of the immune activation in the first half of life have been overshadowed by the explosion of the syndrome's negative effects in later life.
Charles University Prague Czech Republic
Department of Pathology Albert Einstein College of Medicine Bronx NY USA
James J Peters VA Medical Center Mount Sinai Medical Center Health System Bronx NY USA
Citace poskytuje Crossref.org
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