7-Chloro-4-(phenylselanyl) quinoline reduces renal oxidative stress induced by oxaliplatin in mice

被引:7
|
作者
da Motta, Ketlyn P. [1 ,2 ]
Lemos, Briana B. [1 ,2 ]
Paltian, Jaini J. [1 ]
Dos Reis, Angelica S. [1 ]
Blodorn, Gustavo B. [3 ]
Alves, Diego [3 ]
Luchese, Cristiane [1 ]
Wilhelm, Ethel A. [1 ,2 ]
机构
[1] Univ Fed Pelotas, UFPel, CCQFA, Lab Pesquisa Farmacol Bioquim LaFarBio, POB 354, BR-96010900 Pelotas, RS, Brazil
[2] Univ Fed Pelotas, UFPel, Ctr Ciencias Quim Farmaceut & Alimentos, Curso Bacharelado Quim Forense, BR-96010900 Pelotas, RS, Brazil
[3] Univ Fed Pelotas, UFPel, CCQFA, Lab Sintese Organ Limpa LASOL, POB 354, BR-96010900 Pelotas, RS, Brazil
关键词
oxaliplatin; selenium; nephroprotection; quinoline; oxidative stress; AMINOLEVULINATE DEHYDRATASE; PLATINUM COMPOUNDS; REDOX HOMEOSTASIS; NA+/K+-ATPASE; NA/K-ATPASE; MECHANISMS; CHEMOTHERAPY; GLUTATHIONE; CISPLATIN; ORGANOSELENIUM;
D O I
10.1139/cjpp-2021-0090
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The object of this study was to evaluate the relationship between oxidative damage induced by oxaliplatin (OXA) and the therapeutic potential of 7-chloro-4-(phenylselanyl) quinoline (4-PSQ) in kidney of mice. Mice received OXA (10 mg/kg) or vehicle intraperitoneally (days 0 and 2). Oral administration of 4-PSQ (1 mg/kg) or vehicle was performed on days 2 to 14. On day 15 the animals were euthanized and the kidneys and blood were collected. The effect of OXA and (or) 4-PSQon urea, thiobarbituric acid reactive species, nonprotein thiol (NPSH), and protein carbonyl (PC) levels were investigated. Moreover, renal superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), delta-aminolevulinic acid dehydratase (delta-ALA-D), and Na+, K+ ATPase activities were evaluated. Our findings revealed an increase on urea levels and significant renal oxidative damage in OXA-induced mice. OXA exposure increased SOD, CPx, and GST activities and caused a reduction on NPSH levels and CAT and GR activities. Na+,K+ ATPase and delta-ALA-D activities were reduced by OXA. 4-PSQ decreased plasmatic urea levels and renal oxidative damage. SOD, CPx, CAT, GR, and Na+, K+ ATPase activities were restored by 4-PSQ 4-PSQ may be a good prototype for the treatment of OXA-induced renal injury.
引用
收藏
页码:1102 / 1111
页数:10
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