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首页> 外文期刊>Pesticide science >Comparative metabolism and disposition of 14C‐benzyl cypermethrin in quail, rat and mouse
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Comparative metabolism and disposition of 14C‐benzyl cypermethrin in quail, rat and mouse

机译:14C-苄基氯氰菊酯在鹌鹑、大鼠和小鼠中的代谢和处置比较

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AbstractThe excretion and metabolism of cis + trans‐14C‐benzyl cypermethrin has been compared in quail, rat and mouse. Radioactivity was rapidly eliminated by quail dosed orally with 14Ccypermethrin (2 mg kg−1), as was the case in the rat and the mouse. When the birds were dosed intraperitoneally (IP) with the14C‐labelled pyrethroid, radioactivity was excreted more slowly than after oral dosing, and almost 20 of the IP dose of14C remained in the tissues after 7 days. Both mammalian species excreted 14Ccypermethrin more rapidly than did the avian species after IP administration, and less than 6 of the dose remained in their tissues after several days. The biotransformation of the pyrethroid was more complex in the avian species (34 metabolites) than in the two mammals (some 10 metabolites in each species). In quail the predominant reactions were ester bond cleavage of cypermethrin together with either aromatic hydroxylation or amino acid conjugation of the 3‐phenoxybenzyl moiety. The hydroxylated derivatives were eliminated mainly as sulphates. 3‐Phenoxybenzoic acid was conjugated with a variety of amino acids including glycine, taurine, glutamic acid, serine, α‐N‐acetylornithine and the dipeptide glycylualine. The last two conjugations are unique to avian species. The major metabolite of cypermethrin in the rat was the sulphate conjugate of 3‐(14‐hydroxyphenoxy)benzoic acid, whereas in the mouse the major products were 3‐phenoxybenzoic acid and its taurine conjugate. Thus, in the mammalian species where hydroxylation was maximal, amino acid conjugation was a minor metabolic route und vice versa. However, in the quail, aromatic hydroxylation and amino acid conjugation of the 3‐phenoxybenzyl moiety of cypermethrin were both major reactions. The influence of the rates and sites of metabolism, and of the enzymology of amino acid conjugation, in determining this species difference are discussed. The rapid metabolism of cypermethrin to a variety of polar conjugates that are readily excreted, together with the low brain sensitivity of birds compared with mammals to its neurotoxic effects, explains the low acute toxicity of this py
机译:摘要比较了顺式+反式-[14C-苄基]氯氰菊酯在鹌鹑、大鼠和小鼠中的排泄和代谢。鹌鹑口服[14C]氯氰菊酯(2mg kg-1)迅速消除放射性,就像大鼠和小鼠的情况一样。当禽类腹膜内(IP)给药14C标记的拟除虫菊酯时,放射性排泄速度比口服给药后慢,7天后14C的IP剂量的近20%保留在组织中。两种哺乳动物在IP给药后排泄[14C]氯氰菊酯的速度都比禽类快,几天后只有不到6%的剂量留在它们的组织中。拟除虫菊酯的生物转化在鸟类中(34种代谢物)比在两种哺乳动物中(每个物种约10种代谢物)更复杂。在鹌鹑中,主要反应是氯氰菊酯的酯键裂解以及 3-苯氧基苄基部分的芳香族羟基化或氨基酸偶联。羟基化衍生物主要以硫酸盐的形式被淘汰。3-苯氧基苯甲酸与多种氨基酸偶联,包括甘氨酸、牛磺酸、谷氨酸、丝氨酸、α-N-乙酰氯鸟氨酸和二肽甘氨酰丙氨酸。最后两个共轭是鸟类所独有的。氯氰菊酯在大鼠中的主要代谢产物是3-(14-羟基苯氧基)苯甲酸的硫酸盐偶联物,而在小鼠中,主要产物是3-苯氧基苯甲酸及其牛磺酸偶联物。因此,在羟基化程度最高的哺乳动物物种中,氨基酸偶联是一种次要的代谢途径,反之亦然。然而,在鹌鹑中,氯氰菊酯的3-苯氧基苄基部分的芳香族羟基化和氨基酸偶联都是主要反应。讨论了代谢速率和位点以及氨基酸结合酶学在确定这种物种差异方面的影响。氯氰菊酯对各种极性偶联物的快速代谢,这些偶联物很容易排出体外,与哺乳动物相比,鸟类的大脑对其神经毒性作用的敏感性较低,这解释了这种py的低急性毒性

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