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Neonicotinoids action

Many pesticides are not as novel as they may seem. Some, such as the pyre-throid and neonicotinoid insecticides, are modeled on natural insecticides. Synthetic pyrethroids are related to the natural pyrethrins (see Chapter 12), whereas the neo-nicotinoids share structural features with nicotine. In both cases, the synthetic compounds have the same mode of action as the natural products they resemble. Also, the synthetic pyrethroids are subject to similar mechanisms of metabolic detoxication as natural pyrethrins (Chapter 12). More widely, many detoxication mechanisms are relatively nonspecific, operating against a wide range of compounds that... [Pg.3]

Nicotine is a component of Nicotiana tabacum, the tobacco plant. It is toxic to many insects because of its action upon the nicotinic receptor of acetyl choline. It has served as a model for a new range of insecticides, the neonicotinoids, which also act upon the nicotinic receptor (Salgado 1999). [Pg.7]

Neonicotinoids are potent broad-spectrum insecticides that exhibit contact, stomach and systemic activity. Acetamiprid, imidacloprid, nitenpyram, thiamethoxam and thiacloprid are representatives of the neonicotinoid insecticides (Figure 1). The mechanism of action is similar to that of nicotine, acting on the central nervous system causing irreversible blocking of postsynaptic nicotinic acetylcholine receptors (nAChR). Neonicotinoid insecticides are often categorized as antagonists of the... [Pg.1128]

Acetamiprid is a neonicotinoid insecticide with outstanding systemic activities and a broad insecticidal spectrum. Acetamiprid controls diverse soil and foliar insect pests infesting cotton, sugar beet, vegetables, fruits and other major food crops by both contact and stomach action... [Pg.1242]

The tobacco compound nicotine has been used as an insecticide for over 200 years. It is especially effective against sucking insects, such as aphids, and has excellent contact activity. Related compounds are neonicotinoids (e.g., imidacloprid), which have similar insecticidal activity, but are less toxic to mammals. Nicotine and imidacloprid mimic the action of acetylcholine, which is the major excitatory neurotransmitter in an insect s central nervous system. The action of acetylcholine is stopped by the enzyme acetylcholinesterase, which rapidly breaks down acetylcholine. Nicotine and imidacloprid are also neuroexcitatory, but do so persistendy, since they are not affected by acetylcholinesterase. Overstimulation of the nervous system often leads to convulsions, paralysis, and death. [Pg.238]

Nauen R., Acetylcholine receptors as sites for developing neonicotinoid insecticides, in Biochemical Sites of insecticide action and resistance, Ishaaya, I., Ed., Berlin Springer-Verlag, 2001, p. 77. [Pg.141]

Most importantly, the chart indicates how two classes with new modes of action, the neonicotinoids and strobilurins, both introduced in the last decade, continue to stimulate the market, suggesting that a focus on new modes of action remains an excellent recipe for success. [Pg.13]

The acute toxicity (i.e., lethal potency) of imidacloprid, other neonicotinoids, and related analogs in mammals is most closely related to potency at the 7 nicotinic receptor subtype, followed in order by potency at 1x4, fSx, 0(3, and aj nicotinic receptors, respectively. However, acute toxicity in mammals involves complex actions (agonist and antagonist) at multiple receptor subtypes and these actions vary greatly with minor changes in chemical structure. [Pg.1379]

Univ., China) presented his recent research results entitled Structure-activity relationship of novel sulfonylurea inhibitors on AHAS . H. Matsumoto (Univ. of Tsukuba, Japan) then introduced his study Mode of action of several classes of herbicides causing photooxi dative injury in plants . The second one dealt with insecticides, where X.-H. Qian (East China Univ. of Science and Technology, China) and K. Matsuda (Kinki Univ., Japan) presented their recent findings on chemistry and biochemistry of neonicotinoids. Interchange between Pesticide Science Societies of Korea and Japan was also maintained at a seminar entitled Current and future R D activities in agrochemical area in Korea and Japan . [Pg.476]

Two of the three main classes of insecticides exert their neurotoxic effects through action on the cholinergic system. This is the case for the new class of neonicotinoids, which are known to act on the nicotinic acetylchohne... [Pg.85]

Neonicotinoids are insecticides acting on insect nAChRs (1). For a long time they are very effective on commercially important Hemipteran pest species such as aphids, whiteflies and planthoppers, but also control Coleopteran and some Lepidopteran pests (/). The biochemical mode of action (MoA) of neonicotinoids has been studied and characterized extensively in the past 10 years. Ail neonicotinoids act selectively as agonists at the insect nAChRs and they are part of a single MoA group as defmed by the Insecticide Resistance Action Committee (IRAC an Expert Conunittee of Crop Life) for resistance management purposes (2). Today the neonicotinoids are ... [Pg.52]

Neonicotinoid insecticides have experienced a most remarkable and steady increase in use since their market introduction in 1991, now exceeding 10% of the total insecticide market 1-3). An overview of these products is given in Table I (cf. 4). The major advantages of the new products over the previously preferred organophosphates are a novel chemistry, a new mode of action, systemic action and human safety. The systemic activity makes them the insecticide class of choice for the control of plant sucking pests. [Pg.67]

While members of the neonicotinoid class of insecticides share a number of structural and physico-chemical properties, the individual compounds provide a remarkable diversity of structural details, which may confer biological differences in their action 13). [Pg.69]

Yamamoto I, Yabuta G, Tomizawa M, Saito T, Miyamoto T, Kagabu S (1995) Molecular mechanism for selective toxicity of nicotinoids and neonicotinoids. Nippon Noyaku Gakkaishi 20 33 0 Yamamoto I, Tomizawa M, Saito T, Miyamoto T, Walcott EC, Sunrikawa K (1998) Structural factors contributing to insecticidal and selective actions of neonicotinoids. Arch Insect Biochem Physiol 37 24-32... [Pg.212]

Mechanism of Selective Actions of Neonicotinoids on Insect Nicotinic Acetylcholine Receptors... [Pg.172]

Structural and Physicochemical Properties of Neonicotinoids Contributing to Their Selective Actions... [Pg.174]


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