Paradoxical Effect of Grape Pomace Extract on Cisplatin-Induced Acute Kidney Injury in Rats

被引:6
|
作者
Neag, Maria Adriana [1 ]
Mitre, Calin Iosif [2 ]
Mitre, Andrei Otto [3 ]
Morhan, Vlad [3 ]
Catinean, Adrian [4 ]
Botan, Emil Claudiu [5 ]
Melincovici, Carmen Stanca [6 ]
Muntean, Dana Maria [7 ]
Buzoianu, Anca Dana [1 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Pharmacol Toxicol & Clin Pharmacol Dept, 23 Marinescu St, Cluj Napoca 400337, Romania
[2] Iuliu Hatieganu Univ Med & Pharm, Dept Anaesthesiol & Intens Care, 19-21 Croitorilor St, Cluj Napoca 400162, Romania
[3] Iuliu Hatieganu Univ Med & Pharm, Fac Med, 8 Babes St, Cluj Napoca 400012, Romania
[4] Iuliu Hatieganu Univ Med & Pharm, Dept Internal Med, 3-5 Clinicilor St, Cluj Napoca 400006, Romania
[5] Cty Emergency Hosp Cluj Napoca, 3-5 Clinicilor St, Cluj Napoca 400006, Romania
[6] Iuliu Hatieganu Univ Med & Pharm, Histol Dept, 4-6 Pasteur St, Cluj Napoca 400349, Romania
[7] Iuliu Hatieganu Univ Med & Pharm, Dept Pharmaceut Technol & Biopharmaceut, 12 Ion Creanga St, Cluj Napoca 400010, Romania
关键词
cisplatin; grape extract; resveratrol; nephrotoxicity; COPPER TRANSPORTER CTR1; INDUCED NEPHROTOXICITY; MITOCHONDRIAL-MEMBRANE; OXIDATIVE STRESS; SEED EXTRACT; RENAL INJURY; RED WINE; ANTIOXIDANT; RESVERATROL; CHEMOTHERAPY;
D O I
10.3390/pharmaceutics11120656
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cisplatin is one of the most used drugs in the therapy of different types of cancer. However, its use is limited by nephrotoxicity. This study investigated the effects of a commercially available grape pomace extract (GE) from Vitis vinifera on cisplatin-induced kidney toxicity in rats. Sixty-four male Wistar albino rats were randomly divided into eight groups. Groups 1-3 were controls, receiving 0.9% saline and doses 1 and 2 of GE respectively. Cisplatin was given to groups 4-8. Two groups received pretreatment with GE, while another two groups received pre- and post-treatment with GE. Blood samples were collected and all animals sacrificed. Kidneys were harvested for histopathological analysis. GE significantly increased blood creatinine and urea levels, the severity of kidney histopathological damage, and mortality in all cisplatin groups, except for group 7 which received pre- and post-treatment with a low dose of GE. Renal toxicity was determined by mortality and severe histopathological renal lesions. Additionally, the serum total antioxidant capacity (TAC) was not significantly modified in the treated groups compared to the control. These results indicate that the GE did not have a protective effect on cisplatin-induced nephrotoxicity; on the contrary, GE accentuated the toxic effect of cisplatin.
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页数:12
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