Neonicotinoid Metabolism: Compounds, Substituents, Pathways, Enzymes, Organisms, and Relevance

• Published in: Journal of agricultural and food chemistry Vol. 59; no. 7; pp. 2923 - 2931
• Main Author: Casida, John E
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Washington, DC American Chemical Society 13-04-2011
• Subjects: acetylation; agonists; Aldehyde Oxidase - metabolism; Anabasine - agonists; Animals; Bacteria - enzymology; Biodegradation, Environmental; Biological and medical sciences; chemotypes; Cytochrome P-450 Enzyme System - metabolism; enzymes; Food industries; Fundamental and applied biological sciences. Psychology; hepatotoxicity; hydroxylation; Imidazoles - metabolism; Insecta - enzymology; Insecticide Resistance; Insecticides - metabolism; isozymes; metabolism; metabolites; methylation; Models, Molecular; mutants; neonicotinoid insecticides; Neonicotinoids; Nitro Compounds - metabolism; pest resistance; Receptors, Nicotinic; toxicology; vigor; CYP450; insecticide metabolism; neonicotinoids; thiamethoxam; Aldehyde oxidase; clothianidin; imidacloprid; Organism; Insecticide; Enzyme; Pesticides; Aldehyde; Metabolism
• ISSN: 0021-8561; 1520-5118
• DOI: 10.1021/jf102438c

Neonicotinoids are one of the three principal insecticide chemotypes. The seven major commercial neonicotinoids are readily biodegraded by metabolic attack at their N-heterocyclylmethyl moiety, heterocyclic or acyclic spacer, and N-nitroimine, nitromethylene, or N-cyanoimine tip. Phase I metabolism is largely dependent on microsomal CYP450 isozymes with situ selectivity in hydroxylation, desaturation, dealkylation, sulfoxidation, and nitro reduction. Cytosolic aldehyde oxidase is a nitroreductase for some neonicotinoids. Phase II metabolism involves methylation, acetylation, and formation of glucuronide, glucoside, amino acid, and sulfate- and glutathione-derived conjugates. Some neonicotinoids act as proinsecticides with metabolism to more potent nicotinic agonists. Pest resistance is more commonly due to synergist-reversible CYP450 detoxification than to nAChR mutants or variants. Metabolites in some cases contribute to mammalian hepatotoxicity and carcinogenesis and in others to enhanced plant vigor and stress shields. These relationships explain much of neonicotinoid comparative toxicology and provide the basis for continued and improved safety and effectiveness of this chemotype.