Antifilarial Activity of 1,3-Diarylpropen-1-One: Effect on Glutathione-S-Transferase, a Phase II Detoxification Enzyme

被引:60
作者
Awasthi, Satish K. [1 ]
Mishra, Nidhi [1 ]
Dixit, Sandeep Kumar [1 ]
Singh, Alka [2 ]
Yadav, Marshleen [2 ]
Yadav, Sudhanshu S. [2 ]
Rathaur, Sushma [2 ]
机构
[1] Univ Delhi, Dept Chem, Biol Chem Lab, Delhi 110007, India
[2] Banaras Hindu Univ, Fac Sci, Dept Biochem, Varanasi 221005, Uttar Pradesh, India
关键词
IN-VITRO; ANTIMALARIAL ACTIVITY; LYMPHATIC FILARIASIS; ACTIVATION; DERIVATIVES; EXPRESSION; IVERMECTIN; INHIBITORS; CHALCONES; STRESS;
D O I
10.4269/ajtmh.2009.80.764
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Chalcone derivatives were evaluated for their antifilarial activity on Setaria cervi using glutathione-S-transferase (GST) as a drug target. The compounds 1-(4-benzotriazol-1-yl-phenyl)-3-(4-methoxyphenyl)prop-2-en-1-one (5), and 3-(4-methoxyphenyl)-.1-(4-pyrrolidin-1-yl-phenyl) prop-2-en-1-one (7) showed a significant suppression (P < 0.01) in GST activity of adult female parasite extract at 3 mu M concentration in vitro. However, GST activity was detected along with depletion in GSH level. Except Compounds 1 and 2, all exhibited a significant effect on the motility and viability of adult parasites. Compounds 3- (4-chlorophenyl)-1-(4-piperidin-1-yl-phenyl)prop-2-en-1-one (3),1-(4-benzotriazol-1-yl-phenyl)-3-(4-methoxyphenyl)prop-2-en-1-one (5), and 3-(4-methoxyphenyl)-1-(4-pyrrolidin-1-yl-phenyl) prop-2-en-1-one (7) exhibited major irreversible effects on viability and resulted in parasite death and also inhibited the GST activity by 84-100% in vitro. We report for the first time the antifilarial activity of chalcones on GST of adult parasites. This study also strengthens our previous findings where GST is reported as a potential drug target for antifilarials.
引用
收藏
页码:764 / 768
页数:5
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