Provinol prevents CsA-induced nephrotoxicity by reducing reactive oxygen species, NOS, and NF-kB expression

被引:44
作者
Buffoli, B
Pechánová, O
Kojsová, S
Andriantsitohaina, R
Giugno, L
Bianchi, R
Rezzani, R
机构
[1] Univ Brescia, Dept Biomed Sci & Biotechnol, Div Human Anat, I-25123 Brescia, Italy
[2] Slovak Acad Sci, Inst Normal & Pathol Physiol, Bratislava, Slovakia
[3] Univ Strasbourg 1, Illkirch Graffenstaden, France
关键词
fibrosis; kidney; Provinol; ROS;
D O I
10.1369/jhc.5A6623.2005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cyclosporine A (CsA) use is associated with several side effects, the most important of which is nephrotoxicity that includes, as we previously showed, tubular injury and interstitial fibrosis. Recently, many researchers have been interested in minimizing these effects by pharmacological interventions. To do this, we tested whether the administration of a red wine polyphenol, Provinol (PV), prevents the development of CsA-induced nephrotoxicity. Rats were treated for 21 days and divided into four groups: control; group treated with PV (40 mg/kg/day by oral administration in tap water); group treated with CsA (15 mg/kg/day by subcutaneous injection); group treated with CsA plus PV. CsA produced a significant increase of systolic blood pressure; it did not affect urinary output, but caused a significant decrease in creatinine clearance. These side effects were associated with an increase in conjugated dienes, which are lipid peroxidation products, inducible NO-synthase (iNOS), and nuclear factor (NF)-kB, which are involved in antioxidant damage. However, PV prevented these negative effects through a protective mechanism that involved reduction of both oxidative stress and increased iNOS and NF-kB expression induced by CsA. These results provide a pharmacological basis for the beneficial effects of plant-derived polyphenols against CsA-induced renal damage associated with CsA.
引用
收藏
页码:1459 / 1468
页数:10
相关论文
共 52 条
[21]   Increased activity of nuclear factor-κB participates in cardiovascular remodeling induced by chronic inhibition of nitric oxide synthesis in rats [J].
Kitamoto, S ;
Egashira, K ;
Kataoka, C ;
Koyanagi, M ;
Katoh, M ;
Shimokawa, H ;
Morishita, R ;
Kaneda, Y ;
Sueishi, K ;
Takeshita, A .
CIRCULATION, 2000, 102 (07) :806-812
[22]   POTENTIATION OF LIPID PEROXIDES BY ISCHEMIA IN RAT-BRAIN [J].
KOGURE, K ;
WATSON, BD ;
BUSTO, R ;
ABE, K .
NEUROCHEMICAL RESEARCH, 1982, 7 (04) :437-454
[23]   In vitro models to study mechanisms involved in cyclosporine A-mediated glomerular contraction [J].
L'Azou, B ;
Medina, J ;
Frieauff, W ;
Cordier, A ;
Cambar, J ;
Wolf, A .
ARCHIVES OF TOXICOLOGY, 1999, 73 (06) :337-345
[24]   Melatonin prevents cyclosporine-induced nephrotoxicity in isolated and perfused rat kidney [J].
Longoni, B ;
Migliori, M ;
Ferretti, A ;
Origlia, N ;
Panichi, V ;
Boggi, U ;
Filippi, C ;
Cuttano, MG ;
Giovannini, L ;
Mosca, F .
FREE RADICAL RESEARCH, 2002, 36 (03) :357-363
[25]  
Middleton E, 2000, PHARMACOL REV, V52, P673
[26]   Superoxide limits cyclosporine-A-induced formation of peroxynitrite in endothelial cells [J].
Navarro-Antolín, J ;
López-Muñoz, MJ ;
Soria, J ;
Lamas, S .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (08) :702-711
[27]   Salvage of cyclosporine A-induced oxidative stress and renal dysfunction by carvedilol [J].
Padi, SSV ;
Chopra, K .
NEPHRON, 2002, 92 (03) :685-692
[28]   Cyclosporine a nephrotoxicity: Role of thromboxane and reactive oxygen species [J].
Parra, T ;
de Arriba, G ;
Arribas, I ;
de Lema, GP ;
Rodriguez-Puyol, D ;
Rodriguez-Puyol, M .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1998, 131 (01) :63-70
[29]   Cyclosporine increases local glomerular synthesis of reactive oxygen species in rats -: Effect of vitamin E on cyclosporine nephrotoxicity [J].
Parra, T ;
de Arriba, G ;
Conejo, JR ;
Cantero, M ;
Arribas, I ;
Rodríguez-Puyol, D ;
Rodríguez-Puyol, M ;
Carballo, F .
TRANSPLANTATION, 1998, 66 (10) :1325-1329
[30]   Red wine polyphenols prevent cardiovascular alterations in L-NAME-induced hypertension [J].
Pechánová, O ;
Bernátová, I ;
Babál, P ;
Martínez, MC ;
Kyselá, S ;
Stvirtina, S ;
Andriantsitohaina, R .
JOURNAL OF HYPERTENSION, 2004, 22 (08) :1551-1559