Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension
- Michal Pravenec,
- Vaclav Zidek,
- Miroslava Simakova,
- Vladimir Kren,
- Drahomira Krenova,
- Karel Horky
- Charles University,
- Czech Academy of Sciences,
- Institute for Clinical and Experimental Medicine,
- Imperial College Healthcare NHS Trust,
- Wayne State University,
- University of Michigan, Ann Arbor
Open access
Abstract
Disorders of carbohydrate and lipid metabolism have been reported to cluster in patients with essential hypertension and in spontaneously hypertensive rats (SHRs). A deletion in the Cd36 gene on chromosome 4 has recently been implicated in defective carbohydrate and lipid metabolism in isolated adipocytes from SHRs. However, the role of Cd36 and chromosome 4 in the control of blood pressure and systemic cardiovascular risk factors in SHRs is unknown. In the SHR.BN-Il6/Npy congenic strain, we have found that transfer of a segment of chromosome 4 (including Cd36) from the Broom Norway (BN) rat onto the SHR background induces reductions in blood pressure and ameliorates dietary-induced glucose intolerance, hyperinsulinemia, and hypertriglyceridemia. These results demonstrate that a single chromosome region can influence a broad spectrum of cardiovascular risk factors involved in the hypertension metabolic syndrome. However, analysis of Cd36 genotypes in the SHR and stroke-prone SHR strains indicates that the deletion variant of Cd36 was not critical to the initial selection for hypertension in the SHR model. Thus, the ability of chromosome 4 to influence multiple cardiovascular risk factors, including hypertension, may depend on linkage of Cd36 to other genes trapped within the differential segment of the SHR. BN-Il6/Npy strain.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1651-1657 (7 pages)Journal (Volume, Issue Number)
Journal of Clinical Investigation (Volume 103, Issue 12)Publication milestones
- Published - 06/1999
Publication status
ISSN
0021-9738Publication IDs
- Scopus: 0032693236
- PubMed: 10377171
