Prague hereditary hypercholesterolemic (PHHC) rat - a model of polygenic hypercholesterolemia
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
20131941
DOI
10.33549/physiolres.931916
PII: 931916
Knihovny.cz E-zdroje
- MeSH
- ateroskleróza genetika metabolismus patologie MeSH
- cholesterol dietní škodlivé účinky MeSH
- cholesterol krev MeSH
- fenotyp MeSH
- genetická predispozice k nemoci MeSH
- hybridizace genetická MeSH
- hypercholesterolemie krev genetika patologie MeSH
- játra metabolismus patologie MeSH
- krysa rodu Rattus MeSH
- lipoproteiny krev MeSH
- modely nemocí na zvířatech MeSH
- multifaktoriální dědičnost MeSH
- potkani Wistar MeSH
- progrese nemoci MeSH
- ztučnělá játra genetika metabolismus patologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- cholesterol dietní MeSH
- cholesterol MeSH
- lipoproteiny MeSH
Prague hereditary hypercholesterolemic (PHHC) rat - rat strain crossbred from Wistar rats - is a model of hypercholesterolemia induced by dietary cholesterol. Importantly, no bile salts and/or antithyroid drugs need to be added to the diet together with cholesterol to induce hypercholesterolemia. PHHC rats have only modestly increased cholesterolemia when fed a standard chow and develop hypercholesterolemia exceeding 5 mmol/l on 2 % cholesterol diet. Most of the cholesterol in hypercholesterolemic PHHC rats is found in VLDL that become enriched with cholesterol (VLDL-C/VLDL-TG ratio > 1.0). Concurrently, both IDL and LDL concentrations rise without any increase in HDL. PHHC rats do not markedly differ from Wistar rats in the activities of enzymes involved in intravascular remodelation of lipoproteins (lipoprotein and hepatic lipases and lecithin:cholesterol acyltransferase), LDL catabolism, cholesterol turnover rate and absorption of dietary cholesterol. The feeding rats with cholesterol diet results in development of fatty liver in spite of suppression of cholesterol synthesis. However, even though cholesterolemia in PHHC rats is comparable to human hypercholesterolemia, the PHHC rats do not develop atherosclerosis even after 6 months on 2 % cholesterol diet. Importantly, the crossbreeding experiments documented that hypercholesterolemia of PHHC rats is polygenic. To identify the genes that may be involved in pathogenesis of hypercholesterolemia in this strain, the studies of microarray gene expression in the liver of PHHC rats are currently in progress.
Citace poskytuje Crossref.org
Global DNA methylation in rats´ liver is not affected by hypercholesterolemic diet
Experimental models of non-alcoholic fatty liver disease in rats