The protective effect of trimetazidine against cisplatin-induced nephrotoxicity in rats

被引:10
作者
El-Sherbeeny, Nagla A. [1 ,2 ]
Attia, Ghalia M. [3 ,4 ]
机构
[1] Taibah Univ, Coll Pharm, Dept Pharmacol & Toxicol, Univ Rd, Al Madinah Al Munawarah, Saudi Arabia
[2] Suez Canal Univ, Dept Clin Pharmacol, Fac Med, Ismailia, Egypt
[3] Taibah Univ, Fac Med, Dept Anat, Al Madinah Al Munawarah, Saudi Arabia
[4] Mansoura Univ, Fac Med, Dept Histol & Cell Biol, Mansoura, Egypt
关键词
cisplatin; oxidative stress; trimetazidine; nephrotoxicity; NF-kappa B; NECROSIS-FACTOR-ALPHA; INDUCED INJURY; RENAL-FAILURE; IN-VIVO; DYSFUNCTION; APOPTOSIS; ANTIOXIDANTS; INFLAMMATION; REPERFUSION; ATTENUATION;
D O I
10.1139/cjpp-2015-0472
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nephrotoxicity is a dose-limiting side effect of cisplatin (CSP). The study investigated the possible protective role of trimetazidine (TMZ) against CSP-induced nephrotoxicity in rats. Rats were divided into four groups; control, TMZ, CSP, and CSP + TMZ. The CSP group showed significant deterioration in kidney function with structural changes in the form of interstitial hemorrhage, glomeruli shrinkage and peritublar capillary congestion, tubular cells vacuolation, pyknosis, shedding and necrosis, and inflammatory cell infiltrates, all indicating renal damage. CSP also caused a significant increase in the lipid peroxidation marker malondialdehyde (MDA) levels, renal nuclear factor kappa B (NF-kappa B) DNA-binding activity and protein expression, and tumor necrosis factor alpha (TNF-alpha) and IL-6 levels. Treatment with TMZ before and after CSP injection produced significant improvement of kidney function and histopathology. TMZ treatment also significantly attenuated CSP-induced oxidative stress and suppressed elevated levels of TNF-alpha and IL-6 and NF-kappa B expression and its DNA-binding activity caused by CSP administration. TMZ has a protective effect against CSP-induced nephrotoxicity mediated by reduction of oxidative stress and attenuation of CSP-induced inflammation.
引用
收藏
页码:745 / 751
页数:7
相关论文
共 44 条
[1]   Naringenin attenuates cisplatin nephrotoxicity in rats [J].
Badary, OA ;
Abdel-Maksoud, S ;
Ahmed, WA ;
Owieda, GH .
LIFE SCIENCES, 2005, 76 (18) :2125-2135
[2]  
Cristina de L.C., 2013, ISRN PHARM, V2013, DOI [10.1155/2013/605640, DOI 10.1155/2013/605640]
[3]   Pre-treatment with cardamonin protects against cisplatin-induced nephrotoxicity in rats: Impact on NOX-1, inflammation and apoptosis [J].
El-Naga, Reem N. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 274 (01) :87-95
[4]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[5]   USE OF AVIDIN-BIOTIN INTERACTION IN IMMUNOENZYMATIC TECHNIQUES [J].
GUESDON, JL ;
TERNYNCK, T ;
AVRAMEAS, S .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1979, 27 (08) :1131-1139
[6]   Transcription factor-κB (NF-κB) and renal disease [J].
Guijarro, C ;
Egido, J .
KIDNEY INTERNATIONAL, 2001, 59 (02) :415-424
[7]   Betaine supplementation mitigates cisplatin-induced nephrotoxicity by abrogation of oxidative/nitrosative stress and suppression of inflammation and apoptosis in rats [J].
Hagar, Hanan ;
El Medany, Azza ;
Salam, Reem ;
El Medany, Gamila ;
Nayal, Omina A. .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2015, 67 (02) :133-141
[8]  
Hanigan Marie H, 2003, Cancer Ther, V1, P47
[9]   The antianginal drug trimetazidine shifts cardiac energy metabolism from fatty acid oxidation to glucose oxidation by inhibiting mitochondrial long-chain 3-ketoacyl coenzyme A thiolase [J].
Kantor, PF ;
Lucien, A ;
Kozak, R ;
Lopaschuk, GD .
CIRCULATION RESEARCH, 2000, 86 (05) :580-588
[10]   Attenuation of renal ischemia-reperfusion injury by trimetazidine:: Evidence of an in vivo antioxidant effect [J].
Kaur, H ;
Padi, SSV ;
Chopra, K .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2003, 25 (10) :803-809