Superoxide inhibits neuronal nitric oxide synthase influences on afferent arterioles in spontaneously hypertensive rats

被引:40
作者
Ichihara, A [1 ]
Hayashi, M [1 ]
Hirota, N [1 ]
Saruta, T [1 ]
机构
[1] Keio Univ, Sch Med, Dept Internal Med, Shinjuku Ku, Tokyo 1608582, Japan
关键词
Tempol; nitric oxide synthase; arterioles; rats; spontaneously hypertensive; kidney;
D O I
10.1161/01.HYP.37.2.630
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
This study was designed to determine the influence of increased superoxide anion in neuronal nitric oxide synthase (nNOS)-dependent regulation of afferent arterioles in spontaneously hypertensive rats (SHR). Afferent arteriolar diameters of male Wistar-Kyoto rats (WKY) and SHR were assessed in vitro with the blood-perfused juxtamedullary nephron technique and averaged 21.6+/-1.6 (n=6) and 18.8+/-1.2 (n=7) mum, respectively. The superoxide dismutase mimetic Tempol (1, 10, and 100 mu mol/L) did not influence afferent arterioles of WKY but significantly increased afferent arteriolar diameters of SHR by 20.6+/-5.5%, 25.2+/-5.4%, and 23.3+/-4.9%, respectively. In WKY (n=6), the nNOS inhibitor S-methyl-L-thiocitrulline (L-SMTC; 10 mu mol/L) and the NOS inhibitor N-omega-nitro-L-arginine (L-NNA; 100 mu mol/L) significantly decreased afferent arteriolar diameters (19.6+/-1.6 mum) by 11.9+/-3.1% and 21.0+/-3.9%, respectively. In SHR (n=7), L-SMTC did not influence afferent arteriolar diameters (21.0+/-1.5 mum), but L-NNA exerted an afferent arteriolar constriction (14.8+/-3.2%) that was similar to the response observed in WKY, Experiments were also performed in the presence of 100 mu mol/L Tempol. In afferent arterioles of WKY (n=6), Tempol treatment did not modulate the basal diameters (21.5+/-1.2 mum) or the constrictor response to L-SMTC (10.6+/-2.1%) or L-NNA (19.3+/-3.3%). In SHR (n=8), Tempol significantly increased afferent arteriolar diameters by 22.5+/-4.3% and enhanced afferent arteriolar constrictor responses to L-SMTC (18.4+/-2.7%) and L-NNA (31.9+/-2.6%). However, the nitric oxide donor S-nitroso-N-acetylpenicillamine (10 mu mol/L), which similarly increased afferent arteriolar diameters (17.2+/-2.3%, n=6), did not affect afferent arteriolar responses to L-SMTC (1.5+/-2.75) or L-NNA (18.6+/-2.3%). These suggest that superoxide anion inhibits the control of afferent arteriolar diameters by nNOS in SHR.
引用
收藏
页码:630 / 634
页数:5
相关论文
共 31 条
[1]   Immunohistochemically detected protein nitration indicates sites of renal nitric oxide release in Goldblatt hypertension [J].
Bosse, HM ;
Bachmann, S .
HYPERTENSION, 1997, 30 (04) :948-952
[2]   DISPARATE EFFECTS OF CA CHANNEL BLOCKADE ON AFFERENT AND EFFERENT ARTERIOLAR RESPONSES TO ANG-II [J].
CARMINES, PK ;
NAVAR, LG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (06) :F1015-F1020
[3]   INVITRO PERFUSION OF JUXTAMEDULLARY NEPHRONS IN RATS [J].
CASELLAS, D ;
NAVAR, LG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (03) :F349-F358
[4]   Increased activity and expression of Ca2+-dependent NOS in renal cortex of ANG II-infused hypertensive rats [J].
Chin, SY ;
Pandey, KN ;
Shi, SJ ;
Kobori, H ;
Moreno, C ;
Navar, LG .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (05) :F797-F804
[5]   ENHANCED TUBULOGLOMERULAR FEEDBACK ACTIVITY IN RATS DEVELOPING SPONTANEOUS HYPERTENSION [J].
DILLEY, JR ;
ARENDSHORST, WJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (04) :F672-F679
[6]   Increased nitric oxide activity in early renovascular hypertension [J].
Dubey, RK ;
Boegehold, MA ;
Gillespie, DG ;
Rosselli, M .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1996, 270 (01) :R118-R124
[7]   ROLE OF NITRIC-OXIDE ON PAPILLARY BLOOD-FLOW AND PRESSURE NATRIURESIS [J].
FENOY, FJ ;
FERRER, P ;
CARBONELL, L ;
GARCIASALOM, M .
HYPERTENSION, 1995, 25 (03) :408-414
[8]   ROLE OF SUPEROXIDE IN THE DEPRESSED NITRIC-OXIDE PRODUCTION BY THE ENDOTHELIUM OF GENETICALLY HYPERTENSIVE RATS [J].
GRUNFELD, S ;
HAMILTON, CA ;
MESAROS, S ;
MCCLAIN, SW ;
DOMINICZAK, AF ;
BOHR, DF ;
MALINSKI, T .
HYPERTENSION, 1995, 26 (06) :854-857
[9]   Nitric oxide synthase activity and renal injury in genetic hypertension [J].
Hayakawa, H ;
Raij, L .
HYPERTENSION, 1998, 31 (01) :266-270
[10]   MECHANISMS FOR ALTERED ENDOTHELIUM-DEPENDENT VASORELAXATION IN ISOLATED KIDNEYS FROM EXPERIMENTAL HYPERTENSIVE RATS [J].
HAYAKAWA, H ;
HIRATA, Y ;
SUZUKI, E ;
SUGIMOTO, T ;
MATSUOKA, H ;
KIKUCHI, K ;
NAGANO, T ;
HIROBE, M ;
SUGIMOTO, T .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :H1535-H1541