Protection by ozone preconditioning is mediated by the antioxidant system in cisplatin-induced nephrotoxicity in rats

被引:46
作者
Borrego, A
Zamora, ZB
González, R
Romay, C
Menéndez, S
Hernández, F
Montero, T
Rojas, E
机构
[1] Natl Ctr Sci Res, Biomed Dept, Ozone Res Ctr, Havana, Cuba
[2] Dr Luis Diaz Soto Surg & Clin Hosp, Havana, Cuba
关键词
ozone oxidative preconditioning; cisplatin-induced nephrotoxicity; antioxidant defenses; lipid peroxidation;
D O I
10.1080/09629350410001664806
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Acute renal failure is a dose-limiting factor of cisplatin chemotherapy. Here, we show the protective effect of ozone oxidative preconditioning against cisplatin-induced renal dysfunction in rats. Ozone oxidative preconditioning is a prophylactic approach, which favors the antioxidant - pro-oxidant balance for preservation of the cell redox state by increasing antioxidant endogenous systems in various in vivo and in vitro experimental models. Aims: To analyze the protective role of ozone oxidative preconditioning against cisplatin-induced nephrotoxicity. Methods: Male Sprague - Dawley rats were pretreated with 15 intrarectal applications of ozone/oxygen mixture at 0.36, 0.72, 1.1, 1.8 and 2.5 mg/kg before cisplatin intraperitoneal injection ( 6 mg/kg). Serum and kidneys were extracted and analyzed 5 days after cisplatin treatment for determinations of the renal content of glutathione, thiobarbituric acid-reactive substances, renal concentration and enzymatic activities of catalase, superoxide dismutase and glutathione peroxidase. Results: Ozone pretreatment prevented the increase in serum creatinine levels, the glutathione depletion and the inhibition of superoxide dismutase, catalase and glutathione peroxidase activities induced by cisplatin in the rat kidney. Also, the renal content of thiobarbituric acid-reactive substances was decreased by ozone therapy. These protective effects of ozone were dose dependent. Conclusions: Intrarectal ozone therapy prevented effectively the renal antioxidant unbalance induced by cisplatin treatment.
引用
收藏
页码:13 / 19
页数:7
相关论文
共 35 条
[1]   Hyperlipidaemia in cisplatin-induced nephrotic rats [J].
Abdel-Gayoum, AA ;
El-Jenjan, KB ;
Ghwarsha, KA .
HUMAN & EXPERIMENTAL TOXICOLOGY, 1999, 18 (07) :454-459
[2]   Protective effects of vitamin E and vitamin C on cisplatin nephrotoxicity in developing rats [J].
Appenroth, D ;
Frob, S ;
Kersten, L ;
Splinter, K ;
Winnefeld, K .
ARCHIVES OF TOXICOLOGY, 1997, 71 (11) :677-683
[3]   CISPLATIN-INDUCED NEPHROTOXICITY AND THE MODULATING EFFECT OF GLUTATHIONE ESTER [J].
BABU, E ;
GOPALAKRISHNAN, VK ;
SRIGANTH, INP ;
GOPALAKRISHNAN, R ;
SAKTHISEKARAN, D .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 144 (01) :7-11
[4]   Oxidant mechanisms in toxic acute renal failure [J].
Baliga, R ;
Ueda, N ;
Walker, PD ;
Shah, SV .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1997, 29 (03) :465-477
[5]   Prevention of renal injury after induction of ozone tolerance in rats submitted to warm ischaemia [J].
Barber, E ;
Menéndez, S ;
León, OS ;
Barber, MO ;
Merino, N ;
Calunga, JL ;
Cruz, E ;
Bocci, V .
MEDIATORS OF INFLAMMATION, 1999, 8 (01) :37-41
[6]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[7]   EFFECTS OF CISPLATIN ON URINARY THROMBOXANE B-2 EXCRETION [J].
BLOCHLDAUM, B ;
PEHAMBERGER, H ;
KURZ, C ;
KYRLE, PA ;
WAGNER, O ;
MULLER, M ;
MONITZER, B ;
EICHLER, HG .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 58 (04) :418-424
[8]   MITOCHONDRIAL INJURY - AN EARLY EVENT IN CISPLATIN TOXICITY TO RENAL PROXIMAL TUBULES [J].
BRADY, HR ;
KONE, BC ;
STROMSKI, ME ;
ZEIDEL, ML ;
GIEBISCH, G ;
GULLANS, SR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (05) :F1181-F1187
[9]  
Davis CA, 2001, J AM SOC NEPHROL, V12, P2683, DOI 10.1681/ASN.V12122683
[10]  
DOBYAN DC, 1980, J PHARMACOL EXP THER, V213, P551