Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension

Michal Pravenec(Czech Academy of Sciences, Institute of Physiology), Václav Zı́dek(Czech Academy of Sciences, Institute of Physiology), Miroslava Šimáková(Czech Academy of Sciences, Institute of Physiology), Vladimı́r Křen(Czech Academy of Sciences, Institute of Physiology), D Křenová(Charles University), K Horký(Charles University), M Jáchymová(Charles University), Blanka Míková(Charles University), L Kazdová(Institute of Clinical and Experimental Medicine), Timothy J. Aitman(Hammersmith Hospital), Paul C. Churchill(Wayne State University), R. Clinton Webb(University of Michigan–Ann Arbor), Nilesh H. Hingarh(University of California, San Francisco), Ying Yang(University of California, San Francisco), Jiaming Wang(University of California, San Francisco), Elizabeth M. St. Lezin(University of California, San Francisco), Theodore W. Kurtz(University of California, San Francisco)
Journal of Clinical Investigation
June 15, 1999
Cited by 109Open Access
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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 Brown 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.


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