Antioxidant effect of diphenyl diselenide against sodium nitroprusside (SNP) induced lipid peroxidation in human platelets and erythrocyte membranes:: An in vitro evaluation

被引:38
|
作者
Posser, Thais
Moretto, Maria Beatriz
Dafre, Alcir Luiz
Farina, Marcelo
Teixeira da Rocha, Joao Batista
Nogueira, Cristina Wayne
Zeni, Gilson
Ferreira, Jovino dos Santos
Leal, Rodrigo Bainy
Franco, Jeferson Luis [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Bioquim, Ctr Ciencias Biol, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Santa Catarina, Dept Ciencias Fisiol, Ctr Ciencias Biol, BR-88040900 Florianopolis, SC, Brazil
[3] Univ Fed Santa Catarina, Ctr Ciencias Saude, Dept Clin Med, Serv Hemoterapia, BR-88040900 Florianopolis, SC, Brazil
[4] Univ Fed Santa Maria, Ctr Ciencias Nat & Exatas, Dept Quim, BR-97105900 Santa Maria, RS, Brazil
关键词
sodium nitroprusside; diphenyl diselenide; lipid peroxidation; platelets; erythrocytes; antioxidants; nitric oxide;
D O I
10.1016/j.cbi.2006.09.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An in vitro evaluation on the antioxidant effect of diphenyl diselenide (PhSe)(2), an organochalcogenide, against sodium nitroprusside (SNP)-induced lipid peroxidation (LPO) was conduced. Human platelets and erythrocyte membranes (ghosts), as well as rat brain homogenates (S-I), were pre-incubated with different concentrations of SNP (0-10 mu M). All SNP concentrations tested significantly increased LPO in human platelets and S I. Platelets were more sensitive to SNP-induced peroxidative damage when compared to S-I. SNP 10 mu M decreased glutathione peroxidase (GPx) activity and did not affect glutathione reductase (GR) and catalase (CAT) activities in human platelets. However, ghosts were insensitive to SNP-induced LPO and no changes on GPx, GR and CAT activities were observed. Diphenyl diselenide significantly protected human platelets against SNP-induced LPO and recovered GPx inactivation. This effect was more evident at (PhSe)(2) concentrations above 2 mu M. The presented results indicate that (PhSe)(2) exerts protective effects on SNP-induced oxidative damage in human blood components and in rat brain. These phenomena seem to be related to its thiol peroxidase-like activity and to a possible direct interaction with SNP and derivatives. Based on our results and on literature, diphenyl diselenide can be pointed as a promising antioxidant molecule. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:126 / 135
页数:10
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