Protection against puromycin aminonucleoside-induced chronic renal disease in the Wistar-Furth rat

被引:20
作者
Erdely, A
Freshour, G
Smith, C
Engels, K
Olson, JL
Baylis, C
机构
[1] W Virginia Univ, Dept Physiol, Morgantown, WV 26506 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
关键词
glomerular filtration rate; proteinuria; nitric oxide deficiency;
D O I
10.1152/ajprenal.00349.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The Wistar-Furth (WF) rat is protected against chronic renal disease (CRD) following 5/6th ablation/infarction vs. the Sprague-Dawley (SD) rat, and protection was associated with preserved renal nitric oxide ( NO) production. This study examined CRD induced with repeated administration of puromycin aminonucleoside ( PAN). SD PAN developed nephrotic range proteinuria (>1 g/24 h), and at 15 wk severe renal injury developed and the glomerular filtration rate (GFR) was reduced to similar to10% of sham. Total NO production, renal NO synthase (NOS) activity, and renal neuronal (n) and medullary endothelial (e) NOS abundance were reduced in the SD PAN. WF PAN exhibited less severe initial proteinuria (> 400 mg/24 h), which abated within weeks, whereas GFR was normal and injury was minimal at 15 wk. Total NO production and renal NOS activity and abundance were significantly elevated compared with SD PAN. NOS mRNA ( nNOS, eNOS, and inducible NOS) was not altered in WF, whereas SD showed significant increases in NOS gene expression with PAN. In conclusion, WF showed resistance to a second model of CRD with maintained renal NOS activity compared with SD.
引用
收藏
页码:F81 / F89
页数:9
相关论文
共 46 条
[1]   Renal and systemic nitric oxide synthesis in rats with renal mass reduction [J].
Aiello, S ;
Noris, M ;
Todeschini, M ;
Zappella, S ;
Foglieni, C ;
Benigni, A ;
Corna, D ;
Zoja, C ;
Cavallotti, D ;
Remuzzi, G .
KIDNEY INTERNATIONAL, 1997, 52 (01) :171-181
[2]   MECHANISMS UNDERLYING TRANSITION FROM ACUTE GLOMERULAR INJURY TO LATE GLOMERULAR SCLEROSIS IN A RAT MODEL OF NEPHROTIC SYNDROME [J].
ANDERSON, S ;
DIAMOND, JR ;
KARNOVSKY, MJ ;
BRENNER, BM ;
CLAREY, LE ;
DOWNES, SJ ;
RILEY, SL ;
SANDQUIST, KJ ;
TROY, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (05) :1757-1768
[3]   ORAL-ADMINISTRATION OF L-ARGININE AND CAPTOPRIL IN RATS PREVENTS CHRONIC-RENAL-FAILURE BY NITRIC-OXIDE PRODUCTION [J].
ASHAB, I ;
PEER, G ;
BLUM, M ;
WOLLMAN, Y ;
CHERNIHOVSKY, T ;
HASSNER, A ;
SCHWARTZ, D ;
CABILI, S ;
SILVERBERG, D ;
IAINA, A .
KIDNEY INTERNATIONAL, 1995, 47 (06) :1515-1521
[4]  
BAYLIS C, 2001, HYPERTENS NEPHROL, V5, P193
[5]  
Brenner BM, 1997, KIDNEY INT, pS124
[6]   INDUCTION OF NITRIC-OXIDE SYNTHASE MESSENGER-RNA EXPRESSION - SUPPRESSION BY EXOGENOUS NITRIC-OXIDE [J].
COLASANTI, M ;
PERSICHINI, T ;
MENEGAZZI, M ;
MARIOTTO, S ;
GIORDANO, E ;
CALDARERA, CM ;
SOGOS, V ;
LAURO, GM ;
SUZUKI, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26731-26733
[7]   Down-regulation of neuronal nitric oxide synthase by nitric oxide after oxygen-glucose deprivation in rat forebrain slices [J].
De Alba, J ;
Cárdenas, A ;
Moro, MA ;
Leza, JC ;
Lorenzo, P ;
Boscá, L ;
Lizasoain, I .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (01) :248-254
[8]  
DIAMOND JR, 1986, AM J PATHOL, V122, P481
[9]  
Erdely A, 2003, J AM SOC NEPHROL, V14, P2526, DOI 10.1097/01.ASN.0000086476.48686.7D
[10]   Sexual dimorphism in the aging kidney: Effects on injury and nitric oxide system [J].
Erdely, A ;
Greenfeld, Z ;
Wagner, L ;
Baylis, C .
KIDNEY INTERNATIONAL, 2003, 63 (03) :1021-1026