Region of rat chromosome 8 determines complex nutrigenetic interactions under conditions of sucrose and cholesterol diets
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
17066744
Knihovny.cz E-zdroje
- MeSH
- cholesterol dietní aplikace a dávkování MeSH
- chromozomy rostlin MeSH
- fyziologie výživy zvířat genetika MeSH
- glukózový toleranční test MeSH
- glykogen biosyntéza MeSH
- inzulin farmakologie MeSH
- konzumní sacharóza aplikace a dávkování MeSH
- krevní glukóza analýza MeSH
- krysa rodu Rattus MeSH
- lipogeneze účinky léků MeSH
- metabolismus lipidů * genetika MeSH
- potkani inbrední SHR MeSH
- savčí chromozomy * MeSH
- zvířata kongenní MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cholesterol dietní MeSH
- glykogen MeSH
- inzulin MeSH
- konzumní sacharóza MeSH
- krevní glukóza MeSH
We have previously established a congenic strain SHR-Lx that carries a differential segment of rat chromosome 8 introgressed from a model of metabolic syndrome--the polydactylous rat strain--on the genomic background of spontaneously hypertensive rat (SHR). We compared the glucose tolerance and lipid profile of adult SHR and SHR-Lx males under conditions of standard diet and diets enriched in sucrose and cholesterol, respectively. While there was no evident difference between the SHR and SHR-Lx on standard diet, the one-week sucrose administration revealed the congenic strain sensitivity to carbohydrate-induced dyslipidemia conferred by the differential segment with only mild derangement of glucose tolerance. On the other hand, the high-cholesterol diet administration for three-weeks resulted in a contrasting pattern as the congenic strain displayed significantly lower concentrations of free fatty acids and improved glucose tolerance compared to SHR. After one-month washout period, the SHR-Lx showed higher insulin, triglyceride and cholesterol concentrations together with diminished insulin sensitivity of visceral adipose tissue. In summary, we have identified a genomic region syntenic to human chromosome 11q23, which determines complex nutrigenetic interactions under conditions of sucrose- and cholesterol-enriched diets.