The antiparasitic isoxazoline A1443 is a potent blocker of insect ligand-gated chloride channels

被引:229
作者
Ozoe, Yoshihisa [1 ]
Asahi, Miho [2 ]
Ozoe, Fumiyo [1 ]
Nakahira, Kunimitsu [2 ]
Mita, Takeshi [3 ]
机构
[1] Shimane Univ, Dept Life Sci & Biotechnol, Matsue, Shimane 6908504, Japan
[2] Nissan Chem Ind Co Ltd, Biol Res Labs, Saitama 3490294, Japan
[3] Nissan Chem Ind Co Ltd, Chem Res Labs, Chiba 2748507, Japan
关键词
GABA; Glutamate; Ligand-gated ion channel; Parasiticide; Receptor; GAMMA-AMINOBUTYRIC ACID; FIPRONIL; RECEPTOR; ANTAGONISTS; ELEGANS; TARGET; SITE;
D O I
10.1016/j.bbrc.2009.11.131
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
A structurally unique isoxazoline class compound, A1443, exhibits antiparasitic activity against cat fleas and dog ticks comparable to that of the commercial ectoparasiticide fipronil This isoxazoline compound inhibits specific binding of the gamma-aminobutyric acid (GABA) receptor channel blocker [H-3]4'-n-propylbicycloorthobenzoate (EBOB) to housefly-head membranes, with an IC50 value of 455 pM. In contrast, the IC50 value in rat-brain membranes is >10 mu M To study the mode of action ofthis isoxazoline, we utilized MdGBC1 and MdGluC1 cDNAs, which encode the subunits of housefly GABA- and glutamate-gated chloride channels, respectively. Two-electrode voltage clamp electrophysiology was used to confirm that A1443 blocks GABA- and glutamate-induced chloride cut rents in Xenopus oocytes expressing MdGBC1 or MdGluC1 channels, with IC50 values of 5.32 and 79 9 nM, respectively Blockade by A1443 was observed in A2'S MdGBC1 and S2'A-MdGluCl mutant channels at levels similar to those of the respective wild-types, and houseflies expressing A2'S-MdGBCl channels were as susceptible to A1443 as standard houseflies. These findings indicate that A1443 is a novel and specific blocker of insect ligand-gated chloride channels. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:744 / 749
页数:6
相关论文
共 21 条
[1]   Synthesis and structure-activity relationships of 1-phenyl-1H-1,2,3-triazoles as selective insect GABA receptor antagonists [J].
Alam, MS ;
Kajiki, R ;
Hanatani, H ;
Kong, XY ;
Ozoe, F ;
Matsui, Y ;
Matsumura, F ;
Ozoe, Y .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (04) :1361-1372
[2]   HOUSE-FLY HEAD GABA-GATED CHLORIDE CHANNEL - TOXICOLOGICALLY RELEVANT BINDING-SITE FOR AVERMECTINS COUPLED TO SITE FOR ETHYNYLBICYCLOORTHOBENZOATE [J].
DENG, YL ;
CASIDA, JE .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1992, 43 (02) :116-122
[3]   HOUSE-FLY BRAIN GAMMA-AMINOBUTYRIC ACID-GATED CHLORIDE CHANNEL - TARGET FOR MULTIPLE CLASSES OF INSECTICIDES [J].
DENG, YL ;
PALMER, CJ ;
CASIDA, JE .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1991, 41 (01) :60-65
[4]   Functional characterization of Musca glutamate- and GABA-gated chloride channels expressed independently and coexpressed in Xenopus oocytes [J].
Eguchi, Y. ;
Ihara, M. ;
Ochi, E. ;
Shibata, Y. ;
Matsuda, K. ;
Fushiki, S. ;
Sugama, H. ;
Hamasaki, Y. ;
Niwa, H. ;
Wada, M. ;
Ozoe, F. ;
Ozoe, Y. .
INSECT MOLECULAR BIOLOGY, 2006, 15 (06) :773-783
[5]   A POINT MUTATION IN A DROSOPHILA GABA RECEPTOR CONFERS INSECTICIDE RESISTANCE [J].
FFRENCHCONSTANT, RH ;
ROCHELEAU, TA ;
STEICHEN, JC ;
CHALMERS, AE .
NATURE, 1993, 363 (6428) :449-451
[6]   INHIBITION OF GAMMA-AMINOBUTYRIC ACID (GABA)-INDUCED CHLORIDE UPTAKE BY GAMMA-BHC AND HEPTACHLOR EPOXIDE [J].
GHIASUDDIN, SM ;
MATSUMURA, F .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1982, 73 (01) :141-144
[7]   Role of a serine residue (S278) in the pore-facing region of the housefly L-glutamate-gated chloride channel in determining sensitivity to noncompetitive antagonists [J].
Hirata, K. ;
Ishida, C. ;
Eguchi, Y. ;
Sakai, K. ;
Ozoe, F. ;
Ozoe, Y. ;
Matsuda, K. .
INSECT MOLECULAR BIOLOGY, 2008, 17 (04) :341-350
[8]   ACTIONS OF THE INSECTICIDE FIPRONIL, ON DIELDRIN-SENSITIVE AND DIELDRIN-RESISTANT GABA RECEPTORS OF DROSOPHILA-MELANOGASTER [J].
HOSIE, AM ;
BAYLIS, HA ;
BUCKINGHAM, SD ;
SATTELLE, DB .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 115 (06) :909-912
[9]  
Ihara Makoto, 2005, Invertebrate Neuroscience, V5, P157, DOI 10.1007/s10158-005-0008-5
[10]   INTERACTIONS OF LINDANE, TOXAPHENE AND CYCLODIENES WITH BRAIN-SPECIFIC TERT-BUTYLBICYCLOPHOSPHOROTHIONATE RECEPTOR [J].
LAWRENCE, LJ ;
CASIDA, JE .
LIFE SCIENCES, 1984, 35 (02) :171-178