L-ARGININE IMPROVES TRANSMISSION OF PERFUSION-PRESSURE TO THE RENAL INTERSTITIUM IN DAHL SALT-SENSITIVE RATS

被引:52
作者
PATEL, AR
GRANGER, JP
KIRCHNER, KA
机构
[1] UNIV MISSISSIPPI, MED CTR, DEPT MED, JACKSON, MS 39216 USA
[2] UNIV MISSISSIPPI, MED CTR, DEPT PHYSIOL & BIOPHYS, JACKSON, MS 39216 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1994年 / 266卷 / 06期
关键词
PRESSURE-NATRIURESIS; ENDOTHELIUM-DERIVED RELAXING FACTOR; NITRIC OXIDE;
D O I
10.1152/ajpregu.1994.266.6.R1730
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
L-Arginine normalizes pressure natriuresis in Dahl salt-sensitive (DS) rats. To determine the role of renal interstitial hydrostatic pressure (RIHP) in this phenomenon, we measured RIHP determined by servo-null during acute changes in renal perfusion pressure in anesthetized DS rats receiving L-arginine (300 mg.kg(-1).day(-1) ip) or vehicle for 3 wk. Dahl salt-resistant (DR) rats were controls. As observed previously, the slope of the pressure-natriuresis relationship was greater (P < 0.05) in L-arginine-treated DS rats than vehicle DS rats and not different from DR rats. The slope of the relationship between renal perfusion pressure and RIHP was greater (P < 0.05) in DR rats than vehicle DS rats. In L-arginine-treated DS rats the slope of this relationship was greater (P < 0.05) than that in vehicle DS rats and not different from DR rats. Removal of the renal capsule blunted the pressure-natriuresis relationship in L-arginine-treated DS rats but had no effect in vehicle DS rats. Thus L-arginine improves transmission of perfusion pressure into the renal interstitium in DS rats and may contribute to the improved pressure-natriuresis response.
引用
收藏
页码:R1730 / R1735
页数:6
相关论文
共 26 条
[1]  
CARRETERO OA, 1977, MAYO CLIN PROC, V52, P465
[2]   L-ARGININE ABROGATES SALT-SENSITIVE HYPERTENSION IN DAHL RAPP RATS [J].
CHEN, PY ;
SANDERS, PW .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (05) :1559-1567
[3]   LOW RENAL PAPILLARY PLASMA-FLOW IN BOTH DAHL AND KYOTO RATS WITH SPONTANEOUS HYPERTENSION [J].
GANGULI, M ;
TOBIAN, L ;
DAHL, L .
CIRCULATION RESEARCH, 1976, 39 (03) :337-341
[4]   EFFECTS OF RENAL-ARTERY PRESSURE ON INTERSTITIAL PRESSURE AND NA EXCRETION DURING RENAL VASODILATION [J].
GRANGER, JP ;
SCOTT, JW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (05) :F828-F833
[5]   EFFECT OF DIRECT INCREASES IN RENAL INTERSTITIAL HYDROSTATIC-PRESSURE ON SODIUM-EXCRETION [J].
GRANGER, JP ;
HAAS, JA ;
PAWLOWSKA, D ;
KNOX, FG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (04) :F527-F532
[6]   EFFECT OF RENAL PERFUSION-PRESSURE ON SODIUM-REABSORPTION FROM PROXIMAL TUBULES OF SUPERFICIAL AND DEEP NEPHRONS [J].
HAAS, JA ;
GRANGER, JP ;
KNOX, FG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 250 (03) :F425-F429
[7]   MECHANISM OF NATRIURESIS DURING INTRARENAL INFUSION OF PROSTAGLANDINS [J].
HAAS, JA ;
HAMMOND, TG ;
GRANGER, JP ;
BLAINE, EH ;
KNOX, FG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (03) :F475-F479
[8]  
HAAS JA, 1988, AM J PHYSIOL, V255, pF1178
[9]   ROLE OF RENAL INTERSTITIAL HYDROSTATIC-PRESSURE IN NATRIURESIS OF SYSTEMIC NITRIC-OXIDE INHIBITION [J].
HAAS, JA ;
KHRAIBI, AA ;
PERRELLA, MA ;
KNOX, FG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (03) :F411-F414
[10]   ACETYLCHOLINE-INDUCED VASODILATION WITHOUT NATRIURESIS DURING CONTROL OF INTERSTITIAL PRESSURE [J].
HARTUPEE, DA ;
BURNETT, JC ;
MERTZ, JI ;
KNOX, FG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 243 (04) :F325-F329