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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
*Corresponding author for this work
  • 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
Scholary Output:
Contribution to journal
Article
Peer-review

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

Scholary Output:
Contribution to journal
Article
Peer-review

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

Published - 06/1999

ISSN

0021-9738

Publication IDs

  • Scopus: 0032693236
  • PubMed: 10377171

Publication metrics

Metrics

SciVal
FWCI
16.44
SciVal
Author count
17
SciVal
citations
99
SciVal
Paper percentile
93
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.06
Fractional count
16
Fractional count
0.94
Fractional count
1
Fractional count
1
Scopus
citations

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Citation count
101
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36