Genetically determined chloride-sensitive hypertension and stroke

被引:44
作者
Tanaka, M
Schmidlin, O
Yi, SL
Bollen, AW
Morris, RC
机构
[1] Univ Calif San Francisco, Moffitt Hosp, Gen Clin Res Ctr, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Moffitt Hosp, Gen Clin Res Ctr, Dept Pathol, San Francisco, CA 94143 USA
关键词
D O I
10.1073/pnas.94.26.14748
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The stroke-prone spontaneously hypertensive rat (SHRSP) is a genetically determined model of "salt-sensitive" stroke and hypertension whose full phenotypic expression is said to require a diet high in Na+ and low in K+. We tested the hypothesis that dietary Cl- determines the phenotypic expression of the SHRSP. In the SHRSP fed a normal NaCl diet, supplementing dietary K+ with KCI exacerbated hypertension, whereas supplementing either KHCO3 or potassium citrate (KB/C) attenuated hypertension, when blood pressure (BP) aas measured radiotelemetrically, directly and continually. Supplemental KCI, hut not KB/C, induced strokes, which occurred in all and only those rats in the highest quartiles of both BP and plasma renin activity (PRA). PRA was higher with KCI than with KB/C. These observations demonstrate that with respect to both severity of hypertension and frequency of stroke the phenotypic expression of the SHRSP is (i) either increased or decreased, depending on whether the anionic component of the potassium salt supplemented is, or is not, Cl-; (ii) increased by supplementing Cl- without supplementing Na+, and despite supplementing K+; and hence (iii) both selectively Cl--sensitive and Cl--determined. The observations suggest that in the SHRSP selectively supplemented with CI-the likelihood of stroke depends on the extent to which both BP and PRA increase.
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页码:14748 / 14752
页数:5
相关论文
共 46 条
[31]   Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease [J].
Rubattu, S ;
Volpe, M ;
Kreutz, R ;
Ganten, U ;
Ganten, D ;
Lindpaintner, K .
NATURE GENETICS, 1996, 13 (04) :429-434
[32]   INTERRELATION BETWEEN BARORECEPTOR AND MACULA DENSA MECHANISMS IN THE CONTROL OF RENIN SECRETION [J].
SCHOLZ, H ;
VOGEL, U ;
KURTZ, A .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 469 :511-524
[33]  
SEALEY JE, 1995, NEPHRON HETEROGENEIT, P1405
[34]   RENIN-ANGIOTENSIN SYSTEM IN STROKE-PRONE SPONTANEOUSLY HYPERTENSIVE RATS [J].
SHIBOTA, M ;
NAGAOKA, A ;
SHINO, A ;
FUJITA, T .
AMERICAN JOURNAL OF PHYSIOLOGY, 1979, 236 (03) :H409-H416
[35]   A RANDOMIZED CROSSOVER STUDY TO COMPARE THE BLOOD-PRESSURE RESPONSE TO SODIUM LOADING WITH AND WITHOUT CHLORIDE IN PATIENTS WITH ESSENTIAL-HYPERTENSION [J].
SHORE, AC ;
MARKANDU, ND ;
MACGREGOR, GA .
JOURNAL OF HYPERTENSION, 1988, 6 (08) :613-617
[36]   Effects of an angiotensin-converting enzyme inhibitor, a calcium antagonist, and an endothelin receptor antagonist on renal afferent arteriolar structure [J].
Skov, K ;
FengerGron, J ;
Mulvany, MJ .
HYPERTENSION, 1996, 28 (03) :464-471
[38]   EFFECTS OF DIURETICS ON STROKE DEVELOPMENT IN KYOTO-WISTAR STROKE-PRONE SPONTANEOUSLY HYPERTENSIVE RATS [J].
SMEDA, JS ;
TKACHENKO, O .
CLINICAL SCIENCE, 1991, 81 (03) :335-340
[39]   HIGH POTASSIUM DIETS MARKEDLY PROTECT AGAINST STROKE DEATHS AND KIDNEY-DISEASE IN HYPERTENSIVE RATS, A POSSIBLE LEGACY FROM PREHISTORIC TIMES [J].
TOBIAN, L .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1986, 64 (06) :840-848
[40]   BLOOD-PRESSURE AND TUBULOGLOMERULAR FEEDBACK MECHANISM IN CHRONICALLY SALT-LOADED SPONTANEOUSLY HYPERTENSIVE RATS [J].
USHIOGI, Y ;
TAKABATAKE, T ;
HABERLE, DA .
KIDNEY INTERNATIONAL, 1991, 39 (06) :1184-1192