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

被引:101
作者
Pravenec, M
Zidek, V
Simakova, M
Kren, V
Krenova, D
Horky, K
Jachymova, M
Mikova, B
Kazdova, L
Aitman, TJ
Churchill, PC
Webb, RC
Hingarh, NH
Yang, Y
Wang, JM
St Lezin, EM
Kurtz, TW [1 ]
机构
[1] Univ Calif San Francisco, Med Ctr, Dept Lab Med, Box 0134,505 Parnassus Ave,Room L-518, San Francisco, CA 94143 USA
[2] Univ Michigan, Dept Physiol, Ann Arbor, MI 48109 USA
[3] Wayne State Univ, Dept Physiol, Detroit, MI 48201 USA
[4] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, MRC, Clin Sci Ctr,Mol Med Grp, London W12 0NN, England
[5] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Div Natl Heart & Lung Inst, London W12 0NN, England
[6] Inst Clin & Expt Med, Prague 14021, Czech Republic
[7] Charles Univ Prague, Gen Fac Hosp, Fac Med 1, Prague 12000, Czech Republic
[8] Charles Univ Prague, Fac Med 1, Inst Biol & Med Genet, Prague 12800, Czech Republic
[9] Acad Sci Czech Republ, Inst Physiol, CR-14220 Prague, Czech Republic
关键词
D O I
10.1172/JCI6691
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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-I16/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-I16/Npy strain.
引用
收藏
页码:1651 / 1657
页数:7
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