Source:http://linkedlifedata.com/resource/pubmed/id/16822831
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2006-10-4
|
pubmed:abstractText |
We have developed a new, double-congenic rat strain BN-Lx.SHR2, which carries two distinct segments of chromosome 2 introgressed from the spontaneously hypertensive rat strain (SHR) into the genetic background of congenic strain BN-Lx, which was previously shown to express variety of metabolic syndrome features. In 16-wk-old male rats of BN-Lx and BN-Lx.SHR2 strains, we compared their glucose tolerance and triacylglycerol and cholesterol concentrations in 20 lipoprotein subfractions and the lipoprotein particle sizes under conditions of feeding standard and high-sucrose diets. Introgression of two distinct SHR-derived chromosome 2 segments resulted in decreased adiposity together with aggravation of glucose intolerance in the double-congenic strain. The BN-Lx.SHR2 rats were more sensitive to sucrose-induced rise in triacylglycerolemia. Although the total cholesterol concentrations of the two strains were comparable after the standard diet and even lower in BN-Lx.SHR2 after sucrose feeding, detailed analysis revealed that under both dietary conditions, the double-congenic strain had significantly higher cholesterol concentrations in low-density lipoprotein fractions and lower high-density lipoprotein fractions. We established a new inbred model showing dyslipidemia and mild glucose intolerance without obesity, attributable to specific genomic regions. For the first time, the chromosome 2 segments of SHR origin are shown to influence other than blood pressure-related features of metabolic syndrome or to be involved in relevant nutrigenomic interactions.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1531-2267
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
3
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
95-102
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:16822831-Adipose Tissue,
pubmed-meshheading:16822831-Animals,
pubmed-meshheading:16822831-Animals, Congenic,
pubmed-meshheading:16822831-Cholesterol,
pubmed-meshheading:16822831-Chromosomes, Mammalian,
pubmed-meshheading:16822831-Disease Models, Animal,
pubmed-meshheading:16822831-Genomics,
pubmed-meshheading:16822831-Glucose Intolerance,
pubmed-meshheading:16822831-Hypertension,
pubmed-meshheading:16822831-Lipoproteins,
pubmed-meshheading:16822831-Male,
pubmed-meshheading:16822831-Quantitative Trait Loci,
pubmed-meshheading:16822831-Rats,
pubmed-meshheading:16822831-Rats, Inbred SHR,
pubmed-meshheading:16822831-Sucrose,
pubmed-meshheading:16822831-Triglycerides
|
pubmed:year |
2006
|
pubmed:articleTitle |
Novel double-congenic strain reveals effects of spontaneously hypertensive rat chromosome 2 on specific lipoprotein subfractions and adiposity.
|
pubmed:affiliation |
Institute of Biology and Medical Genetics of the First Faculty of Medicine of Charles University and the General Teaching Hospital, Prague, Czech Republic.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|