Neonicotinoids and Other Insect Nicotinic Receptor Competitive Modulators: Progress and Prospects

被引:249
作者
Casida, John E. [1 ]
机构
[1] Univ Calif Berkeley, Dept Environm Sci Policy & Management, Environm Chem & Toxicol Lab, Berkeley, CA 94720 USA
来源
ANNUAL REVIEW OF ENTOMOLOGY, VOL 63 | 2018年 / 63卷
关键词
clothianidin; dinotefuran; imidacloprid; honey bees; nicotinic receptors; thiamethoxam; HONEYBEES APIS-MELLIFERA; HIGH-AFFINITY BINDING; ACETYLCHOLINE-RECEPTOR; ALDEHYDE-OXIDASE; ALPHA-BUNGAROTOXIN; GOLDEN-AGE; IN-VIVO; RESISTANCE; SITE; SELECTIVITY;
D O I
10.1146/annurev-ento-020117-043042
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Neonicotinoids (neonics) are remarkably effective as plant systemics to control sucking insects and for flea control on dogs and cats. The nitroimines imidacloprid, clothianidin, thiamethoxam, and dinotefuran are the leaders among the seven commercial neonics that also include the nitromethylene nitenpyram, the nitromethylene-derived cycloxaprid, and the cyanoimines acetamiprid and thiacloprid. Honey bees are highly sensitive to the nitroimines and nitromethylenes, but the cyanoimines are less toxic. All neonics are nicotinic acetylcholine receptor (nAChR) agonists with a common mode of action, target-site cross-resistance, and much higher potency on insect than mammalian nAChRs at defined binding sites. The structurally related sulfoximine sulfoxaflor and butenolide flupyradifurone are also nAChR agonists, and the mesoionic triflumezopyrim is a nAChR competitive modulator with little or no target-site cross-resistance. Some neonics induce stress tolerance in plants via salicylate-associated systems. The neonics in general are readily metabolized and, except for pollinators, have favorable toxicological profiles.
引用
收藏
页码:125 / 144
页数:20
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