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
相关论文
共 50 条
  • [31] ABSOLUTE-CONFIGURATION OF THE ENANTIOMERS OF 7-CHLORO-4-[[4-(DIETHYLAMINO)-1-METHYLBUTYL]AMINO]QUINOLINE (CHLOROQUINE)
    CRAIG, JC
    BHARGAVA, HN
    EVERHART, ET
    LABELLE, B
    OHNSORGE, U
    WEBSTER, RV
    JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (06): : 1167 - 1170
  • [32] 7-Chloro-4-[(E)-2-(3,4,5-trimethoxy-benzylidene)hydrazin-1-yl]quinoline
    Ferreira, Marcelle de Lima
    de Souza, Marcus V. N.
    Wardell, Solange M. S. V.
    Tiekink, Edward R. T.
    Wardell, James L.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O1214 - +
  • [33] 7-Chloro-4-[(E)-2-(2-methoxybenzylidene)hydrazin-1-yl]quinoline monohydrate
    de Souza, Marcus V. N.
    Howie, R. Alan
    Tiekink, Edward R. T.
    Wardell, James L.
    Wardell, Solange M. S. V.
    Kaiser, Carlos R.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2010, 66 : O698 - U5702
  • [34] Synthesis and evaluation of 7-chloro-4-(piperazin-1-yl)quinoline-sulfonamide as hybrid antiprotozoal agents
    Salahuddin, Attar
    Inam, Afreen
    van Zyl, Robyn L.
    Heslop, Donovan C.
    Chen, Chien-Teng
    Avecilla, Fernando
    Agarwal, Subhash M.
    Azam, Amir
    BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (11) : 3080 - 3089
  • [35] Efficacy of the 7-chloro-4-(3-hydroxy-benzilidenehydrazo) quinoline derivative against infection caused by Leishmania amazonensis
    Ribeiro Antinarelli, Luciana Maria
    Nora de Souza, Marcus Vinicius
    Ferraz Coelho, Eduardo Antonio
    Lima, Wallace Pacienza
    Coimbra, Elaine Soares
    REVISTA DA SOCIEDADE BRASILEIRA DE MEDICINA TROPICAL, 2020, 53 : 1 - 5
  • [36] SYNTHETIC ANTIMALARIALS - THE PREPARATION AND PROPERTIES OF 7-CHLORO-4-(4-DIETHYL-AMINO-1-METHYLBUTYLAMINO)-QUINOLINE (SN-7618)
    DRAKE, NL
    CREECH, HJ
    DRAPER, D
    GARMAN, JA
    HAYWOOD, S
    PECK, RM
    WALTON, E
    VANHOOK, JO
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (07) : 1214 - 1216
  • [37] 7-Chloro-4-[(E)-2-(2,5-dimethoxybenzyl-idene)hydrazin-1-yl]quinoline
    de Souza, Marcus V. N.
    Ferreira, Marcelle de Lima
    Wardell, Solange M. S. V.
    Tiekink, Edward R. T.
    Wardell, James L.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O1244 - +
  • [38] THE PREPARATION OF 7-CHLORO-4-(4-(N-ETHYL-N-BETA-HYDROXYETHYLAMINO)-1-METHYLBUTYLAMINO)-QUINOLINE AND RELATED COMPOUNDS
    SURREY, AR
    HAMMER, HF
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1950, 72 (04) : 1814 - 1815
  • [39] N-[7-Chloro-4-[4-(phenoxymethyl)-1H-1,2,3-triazol-1-yl]quinoline]-acetamide
    Coghi, Paolo
    Ng, Jerome P. L.
    Nasim, Ali Adnan
    Wong, Vincent Kam Wai
    MOLBANK, 2021, 2021 (02)
  • [40] Design, Synthesis, and Cytotoxic Evaluation of Certain 7-Chloro-4-(piperazin-1-yl)quinoline Derivatives as VEGFR-II Inhibitors
    Aboul-Enein, Mohamed Nabil
    El-Azzouny, Aida M. Abd El-Sattar
    Ragab, Fatma Abdel-Fattah
    Hamissa, Mohamed Farouk
    ARCHIV DER PHARMAZIE, 2017, 350 (3-4)