GLUTAMATE RECEPTOR INHIBITORS AS POTENTIAL INSECTICIDES

被引:17
作者
ELDEFRAWI, ME
ANIS, NA
ELDEFRAWI, AT
机构
[1] Department of Pharmacology and Experimental Therapeutics, University of Maryland, School of Medicine, Baltimore
关键词
GLUTAMATE RECEPTORS; PHILANTHOTOXINS; POLYAMINES; NEUROTOXICOLOGY; INSECTICIDES;
D O I
10.1002/arch.940220105
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
Philanthotoxin (PhTX) is a neurotoxic constituent of the paralytic venom of the digger wasp, Philanthus triangulum. PhTX inhibits glutamate receptors of insect muscles mostly as a channel blocker, thereby producing muscle paralysis. Since glutamate receptor blockers may be of value as selective insect control agents, numerous derivatives of PhTX were synthesized and tested for their potencies as inhibitors of insect skeletal muscle glutamate receptors. Structure-activity relationship studies revealed that shortening the polyamine chain length reduced potency, and quaternarization of the nitrogen destroyed it. The potency was increased by a bulky anchoring group with moderate hydrophobicity at the end of the polyamine chain. The conversion of the tryosyl moiety to 3,5-diiodo-tyrosyl also increased potency and so did lengthening the butyryl chain from 4 to 10 carbons. Not only did PhTXs inhibit different subtypes of glutamate receptors, including the mammalian N-methyl-D-aspartate receptor, but also nicotinic receptors of insects and vertebrates. Because of this low selectively, and the hydrophilicity of the derivatives tested, which interferes with their penetration to the target receptor, these compounds cannot be used as insecticides. Nevertheless, the insect skeletal muscle glutamate receptor is a viable target for selective insecticides and major changes in PhTX structure may possibly produce derivatives that can be potential insecticides.
引用
收藏
页码:25 / 39
页数:15
相关论文
共 22 条
[1]  
ANIS N, 1990, J PHARMACOL EXP THER, V254, P764
[2]   STRUCTURE-ACTIVITY-RELATIONSHIPS OF ANALOGS OF THE WASP TOXIN PHILANTHOTOXIN - NONCOMPETITIVE ANTAGONISTS OF QUISQUALATE RECEPTORS [J].
BRUCE, M ;
BUKOWNIK, R ;
ELDEFRAWI, AT ;
ELDEFRAWI, ME ;
GOODNOW, R ;
KALLIMOPOULOS, T ;
KONNO, K ;
NAKANISHI, K ;
NIWA, M ;
USHERWOOD, PNR .
TOXICON, 1990, 28 (11) :1333-1346
[3]   CLONING OF A CDNA FOR A GLUTAMATE RECEPTOR SUBUNIT ACTIVATED BY KAINATE BUT NOT AMPA [J].
EGEBJERG, J ;
BETTLER, B ;
HERMANSBORGMEYER, I ;
HEINEMANN, S .
NATURE, 1991, 351 (6329) :745-748
[4]   STRUCTURE AND SYNTHESIS OF A POTENT GLUTAMATE RECEPTOR ANTAGONIST IN WASP VENOM [J].
ELDEFRAWI, AT ;
ELDEFRAWI, ME ;
KONNO, K ;
MANSOUR, NA ;
NAKANISHI, K ;
OLTZ, E ;
USHERWOOD, PNR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4910-4913
[5]   HIGH-AFFINITY BINDING OF PHENCYCLIDINE (PCP) TO CRAYFISH MUSCLE - DISPLACEMENT BY CALCIUM-ANTAGONISTS [J].
ELDEFRAWI, ME ;
ELFAKAHANY, EF ;
MURPHY, DL ;
ELDEFRAWI, AT ;
TRIGGLE, DJ .
BIOCHEMICAL PHARMACOLOGY, 1982, 31 (15) :2549-2552
[6]   BINDING OF [H-3]-PHENCYCLIDINE TO MEMBRANES FROM HOUSEFLY THORACIC MUSCLES [J].
FILBIN, MT ;
ELDEFRAWI, ME ;
ELDEFRAWI, AT .
ARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY, 1985, 2 (02) :181-190
[7]   SYNTHESIS AND BINDING OF [I-125(2)]PHILANTHOTOXIN-343, [I-125(2)]PHILANTHOTOXIN-343-LYSINE, AND [I-125(2)]PHILANTHOTOXIN-343-ARGININE TO RAT-BRAIN MEMBRANES [J].
GOODNOW, RA ;
BUKOWNIK, R ;
NAKANISHI, K ;
USHERWOOD, PNR ;
ELDEFRAWI, AT ;
ANIS, NA ;
ELDEFRAWI, ME .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (08) :2389-2394
[8]   INACTIVATION OF A QUISQUALATE-SENSITIVE GLUTAMATE RECEPTOR BY PHOTOSENSITIVE ANALOGS OF PHILANTHOTOXIN [J].
GOODNOW, RA ;
NAKANISHI, K ;
SUDAN, HL ;
USHERWOOD, PNR .
NEUROSCIENCE LETTERS, 1991, 125 (01) :62-64
[9]   CA2+ PERMEABILITY OF KA-AMPA GATED GLUTAMATE RECEPTOR CHANNELS DEPENDS ON SUBUNIT COMPOSITION [J].
HOLLMANN, M ;
HARTLEY, M ;
HEINEMANN, S .
SCIENCE, 1991, 252 (5007) :851-853
[10]   SPIDER TOXINS AS TOOLS FOR DISSECTING ELEMENTS OF EXCITATORY AMINO-ACID TRANSMISSION [J].
JACKSON, H ;
USHERWOOD, PNR .
TRENDS IN NEUROSCIENCES, 1988, 11 (06) :278-283