Protective effects of the lipophilic redox conjugate tocopheryl succinyl-ethyl ferulate on HIV replication

被引:4
作者
Edeas, MA
Claise, C
Vergnes, L
Khalfoun, Y
Barthelemy, S
Labidalle, S
Lindenbaum, A
机构
[1] FAC PHARM CHATENAY MALABRY, DEPT CLIN PHARM, F-92242 CHATENAY MALABRY, FRANCE
[2] UNIV TOULOUSE 3, FAC PHARM, LAB SYNTH PHYSICOCHIM & RADIOL, F-31062 TOULOUSE, FRANCE
来源
FEBS LETTERS | 1997年 / 418卷 / 1-2期
关键词
human immunodeficiency virus; oxidative stress; phenolic compound; vitamin E; lipophilic drug;
D O I
10.1016/S0014-5793(97)01335-5
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
Previously, we demonstrated that ferulate ethyl and tocopherol reduced HIV replication, In this study, we investigate whether the conjugation of both compounds (O-tocopheryl succinyl O-ethyl ferulate) can increase HIV inhibition, We show here for the first time that O-tocopheryl succinyl O-ethyl ferulate inhibits 80% of HIV replication (HIV-1 acute infection and HIV transmission), inhibits cell lipoperoxidation and prevents cellular glutathione consumption, Compared to ferulate ethyl and tocopheryl succinyl, O-tocopheryl succinyl O-ethyl ferulate inhibits more HIV replication, This may be due in part to the great increase in the lipophilicity of this compound. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:15 / 18
页数:4
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