Polyenylphosphatidylcholine pretreatment ameliorates ischemic acute renal injury in rats

被引:12
作者
Demirbilek, Savas
Karaman, Abdurrahman
Baykarabulut, Aysun
Akin, Melih
Gurunluoglu, Kubilay
Turkmen, Emine
Tas, Erkan
Aksoy, Rauf Tugrul
Edali, Mehmet Naci
机构
[1] Inonu Univ, Sch Med, Dept Pediat Surg, TR-44280 Malatya, Turkey
[2] Inonu Univ, Sch Med, Dept Biochem, TR-44280 Malatya, Turkey
[3] Inonu Univ, Sch Med, Dept Pathol, TR-44280 Malatya, Turkey
关键词
ischemia reperfusion; kidney; neutrophil infiltration; nuclear factor kappa beta; oxidative stress; polyenylphosphatidylcholine;
D O I
10.1111/j.1442-2042.2006.01397.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aim: Polyenylphosphatidycholine has been demonstrated to have antioxidant, cytoprotective and anti-inflammatory effects. Whether polyenylphosphatidycholine pretreatment affects ischemia/reperfusion-induced renal damage in vivo is not known and was investigated here in rats. Methods: Forty female Sprague-Dawley rats were divided into three groups. Group 1 (n = 10) was given saline (control, sham operated). Group 2 (n = 15) were given saline, and Group 3 (n = 15) were given polyenylphosphatidycholine (100 mg/day for 10 days prior to experiment). Groups 2 and 3 were subjected to bilateral renal ischemia (60 min) followed by reperfusion (6 h). After the reperfusion period, the rats were sacrificed and kidney tissue superoxide dismutase, glutathione, total nitrite and nitrate, malondialdehyde and myeloperoxidase levels, plasma aspartate aminotransferase, blood urea nitrogen and creatinine concentrations, and nuclear factor kappa beta expression were determined. Results: Serum levels of aspartate aminotransferase, blood urea nitrogen and creatinine were significantly decreased (P < 0.05) in the treatment group compared to those in the ischemic group. There were significant differences between treatment and ischemic groups regarding the tissue superoxide dismutase, glutathione, total nitrite and nitrate, malondialdehyde, and myeloperoxidase levels (P < 0.05). In addition, polyenylphosphatidycholine pretreatment reduced nuclear factor kappa beta expression in ischemic kidney tissue. Kidneys obtained from rats pretreated with polyenylphosphatidycholine demonstrated marked reduction of the histological features of renal injury compared to kidneys obtained from Group 2 rats, including a little vacuolization, pyknosis and necrosis. Conclusions: Polyenylphosphatidycholine pretreatment provided significant protection against ischemia/reperfusion injury to the kidney. This treatment could be therapeutic in kidney transplantation and other conditions associated with ischemia/reperfusion injury to the kidney.
引用
收藏
页码:747 / 753
页数:7
相关论文
共 45 条
[1]  
Aleynik SI, 1999, J INVEST MED, V47, P507
[2]   Polyenylphosphatidylcholine corrects the alcohol-induced hepatic oxidative stress by restoring S-adenosylmethionine [J].
Aleynik, SI ;
Lieber, CS .
ALCOHOL AND ALCOHOLISM, 2003, 38 (03) :208-212
[3]  
BEUTLER E, 1975, GLUTATHIONE RED BLOO, P69
[4]   MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER [J].
BRADLEY, PP ;
PRIEBAT, DA ;
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) :206-209
[5]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[6]   Dilinoleoylphosphatidylcholine decreases LPS-induced TNF-α generation in Kupffer cells of ethanol-fed rats:: respective roles of MAPKs and NF-κB [J].
Cao, Q ;
Mak, KM ;
Lieber, CS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (04) :849-853
[7]   Effects of polyhemoglobin-antioxidant enzyme complex on ischemia-reperfusion in money [J].
Chang, EJ ;
Lee, TH ;
Mun, KC ;
Kim, HC ;
Suh, SI ;
Bae, JH ;
Kim, SP ;
Cho, KB ;
Hwang, JS .
TRANSPLANTATION PROCEEDINGS, 2004, 36 (07) :1952-1954
[8]   Differential effects of caspase inhibitors on the renal dysfunction and injury caused by ischemia-reperfusion of the rat kidney [J].
Chatterjee, PK ;
Todorovic, Z ;
Sivarajah, A ;
Mota-Filipe, H ;
Brown, PAJ ;
Stewart, KN ;
Cuzzocrea, S ;
Thiemermann, C .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 503 (1-3) :173-183
[9]  
CORTAS NK, 1990, CLIN CHEM, V36, P1440
[10]  
COTRAN RS, 1996, ROBBINS PATHOLOGIC B, P1