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

被引:61
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
相关论文
共 34 条
[1]   Potent antimalarial activity of newly synthesized substituted chalcone analogs in vitro [J].
Awasthi, Satish K. ;
Mishra, Nidhi ;
Kumar, Brajesh ;
Sharma, Manish ;
Bhattacharya, Amit ;
Mishra, Lokesh C. ;
Bhasin, Virendra K. .
MEDICINAL CHEMISTRY RESEARCH, 2009, 18 (06) :407-420
[2]   PHARMACOLOGY OF IVERMECTIN [J].
BENNETT, JL ;
WILLIAMS, JF ;
DAVE, V .
PARASITOLOGY TODAY, 1988, 4 (08) :226-228
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   GLUTATHIONE TRANSFERASE IN HELMINTHS [J].
BROPHY, PM ;
BARRETT, J .
PARASITOLOGY, 1990, 100 :345-349
[5]   β-carbonyl substituted glutathione conjugates as inhibitors of O-volvulus GST2 [J].
Brophy, PM ;
Campbell, AM ;
van Eldik, AJ ;
Teesdale-Spittle, PH ;
Liebau, E ;
Wang, MF .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (09) :979-981
[6]   LICOCHALCONE-A, A NEW ANTIMALARIAL AGENT, INHIBITS IN-VITRO GROWTH OF THE HUMAN MALARIA PARASITE PLASMODIUM-FALCIPARUM AND PROTECTS MICE FROM P-YOELII INFECTION [J].
CHEN, M ;
THEANDER, TG ;
CHRISTENSEN, SB ;
HVIID, L ;
ZHAI, L ;
KHARAZMI, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (07) :1470-1475
[7]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[8]   Expression and inducibility of alpha, pi, and mu glutathione S-transferase protein and mRNA in murine lung [J].
Forkert, PG ;
D'Costa, D ;
El-Mestrah, M .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (01) :143-152
[9]  
Ginger C D, 1986, Parasitol Today, V2, P38, DOI 10.1016/0169-4758(86)90117-1
[10]  
GOMEZ FJS, 2007, ARCH BIOCHEM BIOPHYS, V457, P150