Chromosome 1 blood pressure QTL region influences renal function curve and salt sensitivity in SHR

被引:13
作者
Lo, M
Liu, KL
Clemitson, JR
Sassard, J
Samani, NJ
机构
[1] Fac Pharm Lyon, Dept Physiol & Pharmacol Clin, CNRS, UMR 5014, F-69373 Lyon 08, France
[2] Univ Leicester, Glenfield Gen Hosp, Dept Cardiol, Leicester LE3 9QP, Leics, England
关键词
genetic hypertension; congenic strain; kidney;
D O I
10.1152/physiolgenomics.00057.2001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
One or more quantitative trait locus (QTL) for blood pressure (BP) exists on rat chromosome 1, in the vicinity of the Sa gene. The present work examined whether this QTL region: 1) alters pressure-natriuresis relationship and 2) affects the BP response to salt load. Male spontaneously hypertensive rats (SHR), Wistar-Kyoto (WKY) rats, and rats from an SHR congenic strain that contains a WKY chromosome 1 segment spanning the BP QTL region (SHR. WKY-Sa) were used. In an acute study in anesthetized animals, renal function was measured at several levels of renal perfusion pressure. In a chronic study, BP was measured in freely moving rats using telemetry during normal and high sodium intake (2% NaCl as drinking water for 2 wk). WKY rats showed a significantly higher glomerular filtration rate and increased pressure-natriuresis compared with SHR. SHR. WKY-Sa also demonstrated an increased glomerular filtration rate and enhanced pressure-natriuresis, associated with a lower tubular sodium reabsorption, compared with SHR. These modifications were accompanied by a lower basal BP in SHR. WKY-Sa compared with SHR and a markedly reduced BP response to salt load. These findings suggest that the BP QTL(s) present in this region of chromosome 1 influences BP and salt sensitivity, at least partly, by modulating pressure-natriuresis.
引用
收藏
页码:15 / 21
页数:7
相关论文
共 31 条
[1]   A NEW METHOD FOR CONTINUOUS CHRONIC MEASUREMENT AND RECORDING OF BLOOD-PRESSURE, HEART-RATE AND ACTIVITY IN THE RAT VIA RADIOTELEMETRY [J].
BROCKWAY, BP ;
MILLS, PA ;
AZAR, SH .
CLINICAL AND EXPERIMENTAL HYPERTENSION PART A-THEORY AND PRACTICE, 1991, 13 (05) :885-895
[2]   Genetic dissection of region around the Sa gene on rat chromosome 1 - Evidence for multiple loci affecting blood pressure [J].
Frantz, S ;
Clemitson, JR ;
Bihoreau, MT ;
Gauguier, D ;
Samani, NJ .
HYPERTENSION, 2001, 38 (02) :216-221
[3]   Successful isolation of a rat chromosome 1 blood pressure quantitative trait locus in reciprocal congenic strains [J].
Frantz, SA ;
Kaiser, M ;
Gardiner, SM ;
Gauguier, D ;
Vincent, M ;
Thompson, JR ;
Bennett, T ;
Samani, NJ .
HYPERTENSION, 1998, 32 (04) :639-646
[4]   Polymorphisms in the carboxy-terminus of the epithelial sodium channel in rat models for hypertension [J].
Grunder, S ;
Zagato, L ;
Yagil, C ;
Yagil, Y ;
Sassard, J ;
Rossier, BC .
JOURNAL OF HYPERTENSION, 1997, 15 (02) :173-179
[5]   HETEROGENEOUS COMPUTER NETWORK FOR REAL-TIME HEMODYNAMIC SIGNAL-PROCESSING [J].
GUSTIN, MP ;
CERUTTI, C ;
PAULTRE, CZ .
COMPUTERS IN BIOLOGY AND MEDICINE, 1990, 20 (03) :205-215
[6]   LONG-TERM ARTERIAL-PRESSURE CONTROL - AN ANALYSIS FROM ANIMAL-EXPERIMENTS AND COMPUTER AND GRAPHIC MODELS [J].
GUYTON, AC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 259 (05) :R865-R877
[7]  
HALL EH, 1996, KIDNEY INT S55, V49, pS35
[8]  
HARRAP SB, 1986, J HYPERTENS, V4, pS249
[9]   S(A) GENE AND BLOOD-PRESSURE COSEGREGATION USING DAHL SALT-SENSITIVE RATS [J].
HARRIS, EL ;
DENE, H ;
RAPP, JP .
AMERICAN JOURNAL OF HYPERTENSION, 1993, 6 (04) :330-334
[10]  
HUBNER N, 1999, HYPERTENSION, V34, P634