Computational and Toxicological Evaluation of Thiamethoxam as Nicotinic Acetylcholine Receptor Modulator Against Cowpea Aphid, Aphis craccivora Koch.

Mohamed Abdelmoteleb, Amany Mohamed, Noha Genidy, Doaa Abdel-Haleem
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Abstract

interaction with AChBP than the co-crystalized ligand (imidacloprid) and good alignment in the active site. THIA indicated different variations in the activities of tested enzymes. Where, aphids treated with LC 50 of THIA increased the biochemical activities of acetylcholinesterase, antioxidant enzymes and peroxidases while decreasing the activity of alpha esterase, carboxylesterase (CarE), glutathione S-transferase and catalase. Therefore, this compound is efficient against sap-sucking pests with good irreversible and specific binding interaction with nicotinic acetylcholine receptor (nAChR) and, consequently, low mammalian toxicity. So, THIA is considered a favourable agent for the management of insect pests.
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噻虫嗪作为烟碱乙酰胆碱受体调节剂对豇豆蚜虫(Aphis craccivora Koch)的计算和毒理学评估
与共晶体配体(吡虫啉)相比,与 AChBP 的相互作用更强,在活性位点的配位更好。THIA 对测试酶的活性有不同的影响。其中,用 LC 50 的 THIA 处理蚜虫会提高乙酰胆碱酯酶、抗氧化酶和过氧化物酶的生化活性,而降低α酯酶、羧酸酯酶(CarE)、谷胱甘肽 S-转移酶和过氧化氢酶的活性。因此,这种化合物能有效地防治吸食树液的害虫,与烟碱乙酰胆碱受体(nAChR)的结合具有良好的不可逆和特异性,因此对哺乳动物的毒性较低。因此,THIA 被认为是一种管理害虫的有利药剂。
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