The ameliorative effects of ceftriaxone and vitamin E against cisplatin-induced nephrotoxicity

被引:36
作者
Abdel-Daim, Mohamed M. [1 ]
Aleya, Lotfi [2 ]
El-Bialy, Badr E. [3 ]
Abushouk, Abdelrahman Ibrahim [4 ]
Alkahtani, Saad [5 ]
Alarifi, Saud [5 ]
Alkahtane, Abdullah A. [5 ]
AlBasher, Gadah [5 ]
Ali, Daoud [5 ]
Almeer, Rafa S. [5 ]
Al-Sultan, Nouf K. [5 ]
Alghamdi, Jawahir [5 ]
Alahmari, Abeer [6 ]
Bungau, Simona G. [7 ]
机构
[1] Suez Canal Univ, Fac Vet Med, Dept Pharmacol, Ismailia 41522, Egypt
[2] Bourgogne Franche Comte Univ, CNRS, UMR 6249, Chronoenvironm Lab, F-25030 Besancon, France
[3] Sadat City Univ, Fac Vet Med, Dept Forens Med & Toxicol, Sadat City, Egypt
[4] Ain Shams Univ, Fac Med, Ramsis St, Cairo 11566, Egypt
[5] King Saud Univ, Coll Sci, Dept Zool, Riyadh, Saudi Arabia
[6] King Khalid Univ, Dept Biol, Coll Sci, Abha, Saudi Arabia
[7] Univ Oradea, Fac Med & Pharm, Dept Pharm, Oradea, Romania
关键词
Ceftriaxone; Cisplatin; Rats; -Tocopherol; Vitamin E; ALPHA-TOCOPHEROL PROTECTS; OXIDATIVE STRESS; INDUCED TOXICITY; ANTIOXIDANT; GLUTATHIONE; MECHANISMS; ACID; COMPLEXES; TISSUES; DAMAGE;
D O I
10.1007/s11356-019-04801-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nephrotoxicity is a common adverse effect of treatment with cisplatin (CDDP). This study was performed to evaluate the antioxidant and nephroprotective efficacy of ceftriaxone (CTX) and vitamin E (Vit.E), alone and in combination against CDDP-induced acute renal injury. Fifty-six male albino rats were equally divided into seven groups, receiving (I) normal saline, (II) CTX (100mg/kg, intraperitoneal [i.p] injection), (III) Vit.E (100mg/kg orally), (IV) CDDP (5mg/kg i.p injection), (V) CDDP plus CTX, (VI) CDDP plus Vit.E, and (VII) CDDP plus CTX in combination with Vit.E. All treatments were administered daily for 10days except CDDP, which was given as a single dose at the sixth day of the study. Compared to normal control rats, CDDP-injected rats showed significantly (p<0.05) higher serum levels of renal injury biomarkers (uric acid, urea, and creatinine) and tumor necrosis factor- (TNF-), as well as increased renal tissue concentrations of malondialdehyde, nitric oxide, and TNF-. Moreover, CDDP administration was associated with significantly lower (p<0.05) renal tissue levels of reduced glutathione and activities of endogenous antioxidant enzymes (glutathione peroxidase, superoxide dismutase, and catalase) and total antioxidant capacity. All these alterations were significantly ameliorated in CDDP-injected rats, receiving CTX and/or Vit.E, compared to rats receiving CDDP alone. Interestingly, the antioxidant and anti-inflammatory effects were more marked in the CTX-Vit.E combination group, compared to groups receiving either drug alone. In conclusion, CTX and Vit.E (especially in combination) could counteract the nephrotoxic effect of CDDP, probably through their antioxidant activities.
引用
收藏
页码:15248 / 15254
页数:7
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