Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Published Online
on August 12, 2002

Hypertension. 2002
Published online before print August 12, 2002, doi: 10.1161/01.HYP.0000029106.10586.4C
A more recent version of this article appeared on September 1, 2002
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
40/3/292    most recent
01.HYP.0000029106.10586.4Cv1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Clemitson, J.-R.
Right arrow Articles by Samani, N. J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Clemitson, J.-R.
Right arrow Articles by Samani, N. J.
Related Collections
Right arrow Animal models of human disease
Right arrow Functional genomics
Right arrow Genetics of cardiovascular disease

Submitted on March 7, 2002
Revised on March 26, 2002

Kidney Specificity of Rat Chromosome 1 Blood Pressure Quantitative Trait Locus Region

Jenny-Rebecca Clemitson; Julian R. Pratt; Simon Frantz; Steven Sacks; and Nilesh J. Samani*

From the Department of Cardiology, University of Leicester (J-R.C., S.F., N.J.S), Leicester, United Kingdom; and Department of Nephrology and Transplantation, Guy's Kings & St Thomas' School of Medicine, Kings College (J.P., S.S), London, United Kingdom.

* To whom correspondence should be addressed. E-mail: njs{at}le.ac.uk.

Abstract—Rat chromosome 1 has a region containing loci that influence blood pressure. In the present study, we investigated whether these loci mediate their effect via the kidney. Taking advantage of the histocompatability between a congenic strain (WKY.SHR-Sa, which contains the relevant chromosomal region from the spontaneously hypertensive rat) and its parental strain, the Wistar-Kyoto rat (WKY), we compared the effect of transplanting a kidney at 5 to 6 weeks of age from either congenic rats or WKY into bilaterally nephrectomized WKY. WKY.SHR-Sa animals and WKY with intact kidneys and with unilateral nephrectomy were studied as controls. Blood pressure was measured at 12, 16, 20, and 25 weeks of age. At all time points, blood pressure was significantly higher (by between 8 to 22 mm Hg, P<0.001) in 2-kidney WKY.SHR-Sa animals compared with WKY. This genotype-related difference was maintained in unilaterally nephrectomized rats. Most importantly, WKY that received transplants from WKY.SHR-Sa rats had significantly higher blood pressure (P<0.001 at all time points) compared with those that received transplants from other WKY. At any age, this difference was between 70% to 100% of the difference observed between the 1-kidney groups. There was no difference in plasma urea or creatinine between groups or evidence of chronic rejection in the cross-transplant group. The findings indicate that the major proportion of the blood pressure effect of loci on rat chromosome 1 is mediated through the kidney, and provide a rational basis for investigating genes located in the relevant chromosomal region and expressed in the kidney as likely candidates.


Key words: hypertension, experimental • genetics • rats, spontaneously hypertensive • genes • transplantation, renal




This article has been cited by other articles:


Home page
Am. J. Physiol. Renal Physiol.Home page
M. J. Pinho, M. P. Serrao, and P. Soares-da-Silva
High-salt intake and the renal expression of amino acid transporters in spontaneously hypertensive rats
Am J Physiol Renal Physiol, May 1, 2007; 292(5): F1452 - F1463.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
J.-R. Clemitson, R. J. Dixon, S. Haines, A. J. Bingham, B. R. Patel, L. Hall, M. Lo, J. Sassard, F. J. Charchar, and N. J. Samani
Genetic Dissection of a Blood Pressure Quantitative Trait Locus on Rat Chromosome 1 and Gene Expression Analysis Identifies SPON1 As a Novel Candidate Hypertension Gene
Circ. Res., April 13, 2007; 100(7): 992 - 999.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
L. J. Mullins, M. A. Bailey, and J. J. Mullins
Hypertension, Kidney, and Transgenics: A Fresh Perspective
Physiol Rev, April 1, 2006; 86(2): 709 - 746.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
B. Joe, N. E. Letwin, M. R. Garrett, S. Dhindaw, B. Frank, R. Sultana, K. Verratti, J. P. Rapp, and N. H. Lee
Transcriptional profiling with a blood pressure QTL interval-specific oligonucleotide array
Physiol Genomics, November 17, 2005; 23(3): 318 - 326.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
R. Rettig and O. Grisk
The Kidney as a Determinant of Genetic Hypertension: Evidence From Renal Transplantation Studies
Hypertension, September 1, 2005; 46(3): 463 - 468.
[Full Text] [PDF]


Home page
HypertensionHome page
C. A. Hinojos, E. Boerwinkle, M. Fornage, and P. A. Doris
Combined Genealogical, Mapping, and Expression Approaches to Identify Spontaneously Hypertensive Rat Hypertension Candidate Genes
Hypertension, April 1, 2005; 45(4): 698 - 704.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
C. A. Mein, M. J. Caulfield, R. J. Dobson, and P. B. Munroe
Genetics of essential hypertension
Hum. Mol. Genet., April 1, 2004; 13(90001): R169 - 175.
[Abstract] [Full Text] [PDF]