Tomizawa_2005_Annu.Rev.Pharmacol.Toxicol_45_247

Reference

Title : Neonicotinoid insecticide toxicology: mechanisms of selective action - Tomizawa_2005_Annu.Rev.Pharmacol.Toxicol_45_247
Author(s) : Tomizawa M , Casida JE
Ref : Annual Review of Pharmacology & Toxicology , 45 :247 , 2005
Abstract :

The neonicotinoids, the newest major class of insecticides, have outstanding potency and systemic action for crop protection against piercing-sucking pests, and they are highly effective for flea control on cats and dogs. Their common names are acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, and thiamethoxam. They generally have low toxicity to mammals (acute and chronic), birds, and fish. Biotransformations involve some activation reactions but largely detoxification mechanisms. In contrast to nicotine, epibatidine, and other ammonium or iminium nicotinoids, which are mostly protonated at physiological pH, the neonicotinoids are not protonated and have an electronegative nitro or cyano pharmacophore. Agonist recognition by the nicotinic receptor involves cation-pi interaction for nicotinoids in mammals and possibly a cationic subsite for interaction with the nitro or cyano substituent of neonicotinoids in insects. The low affinity of neonicotinoids for vertebrate relative to insect nicotinic receptors is a major factor in their favorable toxicological profile.

PubMedSearch : Tomizawa_2005_Annu.Rev.Pharmacol.Toxicol_45_247
PubMedID: 15822177

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Citations formats

Tomizawa M, Casida JE (2005)
Neonicotinoid insecticide toxicology: mechanisms of selective action
Annual Review of Pharmacology & Toxicology 45 :247

Tomizawa M, Casida JE (2005)
Annual Review of Pharmacology & Toxicology 45 :247