Y-chromosome transfer induces changes in blood pressure and blood lipids in SHR
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
Grant support
P01-HL-35018
NHLBI NIH HHS - United States
- MeSH
- Y Chromosome * MeSH
- Diet MeSH
- Fructose administration & dosage MeSH
- Genotype MeSH
- Cholesterol, HDL blood MeSH
- Hypertension blood genetics physiopathology MeSH
- Insulin blood MeSH
- Cardiovascular Diseases etiology MeSH
- Blood Glucose metabolism MeSH
- Blood Pressure physiology MeSH
- Rats MeSH
- Lipids blood MeSH
- Rats, Inbred BN MeSH
- Rats, Inbred SHR MeSH
- Rats, Inbred WKY MeSH
- Risk Factors MeSH
- Body Weight MeSH
- Triglycerides blood MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- Fructose MeSH
- Cholesterol, HDL MeSH
- Insulin MeSH
- Blood Glucose MeSH
- Lipids MeSH
- Triglycerides MeSH
Previous studies with chromosome-Y consomic strains of spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats suggest that a quantitative trait locus for blood pressure regulation exists on chromosome Y. To test this hypothesis in the SHR-Brown Norway (BN) model and to study the effects of chromosome Y on lipid and carbohydrate metabolism, we produced a new consomic strain of SHR carrying the Y chromosome transferred from the BN rat. We found that replacing the SHR Y chromosome with the BN Y chromosome resulted in significant decreases in systolic and diastolic blood pressures in the SHR.BN-Y consomic strain (P<0.05). To elicit possible dietary-induced variation in lipid and glucose metabolism between the SHR progenitor and chromosome-Y consomic strains, we fed rats a high-fructose diet for 15 days in addition to the normal diet. On the high-fructose diet, the SHR.BN-Y consomic rats exhibited significantly increased levels of serum triglycerides and decreased levels of serum HDL cholesterol versus the SHR progenitor rats. Glucose tolerance and insulin/glucose ratios, however, were similar in both strains on both normal and high-fructose diets. These findings provide direct evidence that a gene or genes on chromosome Y contribute to the pathogenesis of spontaneous hypertension in the SHR-BN model. These results also indicate that transfer of the Y chromosome from the BN rat onto the SHR background exacerbates dietary-induced dyslipidemia in SHR. Thus, genetic variation in genes on the Y chromosome may contribute to variation in blood pressure and lipid levels and may influence the risk for cardiovascular disease.
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