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除草剂异丙甲草胺可诱导肝脏细胞色素P450s 2B1/2和3A1/2,但不会诱导甲状腺素-尿苷二磷酸葡萄糖醛酸基转移酶及相关甲状腺活动。

The herbicide metolachlor induces liver cytochrome P450s 2B1/2 and 3A1/2, but not thyroxine-uridine dinucleotide phosphate glucuronosyltransferase and associated thyroid gland activity.

作者信息

Dalton Shana R, Miller Richard T, Meyer Sharon A

机构信息

Department of Toxicology, North Carolina State University, Raleigh, North Carolina, USA.

出版信息

Int J Toxicol. 2003 Jul-Aug;22(4):287-95. doi: 10.1080/10915810305121.

Abstract

Metolachlor (2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl) acetamide) is widely used internationally as a corn and cotton herbicide. The metolachlor effects noted in rats during testing for U.S. pesticide registration include increased liver weight and hepatocarcinogenicity associated with eosinophilic foci. These properties, plus nongenotoxicity, are also characteristic of the prototypical rat liver tumor promoter, phenobarbital. Phenobarbital induces hepatic cytochrome P450s CYP2B1/2 and CYP3A1/2 and thyroxine (T(4))-UDP-glucuronosyltransferase (T(4)-UGT), which enhances thyroxine clearance and thus indirectly increases thyroid gland activity. Because other chloroacetanilide herbicides are known to similarly affect rat thyroid gland, this study tested the hypothesis that metolachlor would have these additional phenobarbital-like effects on liver, especially that of T(4)-UGT induction with consequential stimulation of thyroid gland. Effects of metolachlor, fed to male Sprague-Dawley rats for 14 days at the carcinogenic dose of 3000 ppm, were compared to those of equimolar phenobarbital. Liver microsomal CYP2B1/2 and CYP3A1/2 were probed by immunoblotting and T(4)-UGT was measured enzymatically. Serum T(4), triiodothyronine (T(3)), and thyroid-stimulating hormone (TSH) and thyroid follicular epithelial cell morphology and proliferation were used to assess thyroid gland activity. Metolachlor induced CYP2B1/2 and CYP3A1/2 proteins, but unlike phenobarbital, did not affect T(4)-UGT activity. In agreement, serum T(4), T(3), or TSH were unaffected by metolachlor. Also, no significant effects of metolachlor on thyroid gland morphology or follicular epithelial cell height or proliferation were observed. These data demonstrate that metolachlor is an inducer of hepatic CYP2B1/2 activity. But unlike the prototypical CYP2B1/2 inducer phenobarbital, metolachlor does not cause an increase in T(4)-glucuronidation and thyroid gland activation.

摘要

甲草胺(2-氯-N-(2-乙基-6-甲基苯基)-N-(2-甲氧基-1-甲基乙基)乙酰胺)在国际上广泛用作玉米和棉花除草剂。在美国农药注册测试期间,在大鼠身上观察到的甲草胺的影响包括肝脏重量增加以及与嗜酸性病灶相关的肝癌致癌性。这些特性,加上无基因毒性,也是典型的大鼠肝脏肿瘤促进剂苯巴比妥的特征。苯巴比妥诱导肝细胞色素P450s CYP2B1/2和CYP3A1/2以及甲状腺素(T4)-UDP-葡萄糖醛酸转移酶(T4-UGT),这会增强甲状腺素清除率,从而间接增加甲状腺活性。由于已知其他氯代乙酰苯胺类除草剂会类似地影响大鼠甲状腺,因此本研究检验了以下假设:甲草胺会对肝脏产生这些额外的类似苯巴比妥的影响,尤其是诱导T4-UGT并因此刺激甲状腺。将甲草胺以3000 ppm的致癌剂量喂饲雄性Sprague-Dawley大鼠14天的效果与等摩尔苯巴比妥的效果进行了比较。通过免疫印迹检测肝脏微粒体CYP2B1/2和CYP3A1/2,并通过酶法测量T4-UGT。使用血清T4、三碘甲状腺原氨酸(T3)、促甲状腺激素(TSH)以及甲状腺滤泡上皮细胞形态和增殖来评估甲状腺活性。甲草胺诱导CYP2B1/2和CYP3A1/2蛋白,但与苯巴比妥不同,它不影响T4-UGT活性。与此一致,甲草胺对血清T4、T3或TSH没有影响。此外,未观察到甲草胺对甲状腺形态或滤泡上皮细胞高度或增殖有显著影响。这些数据表明甲草胺是肝脏CYP2B1/2活性的诱导剂。但与典型的CYP2B1/2诱导剂苯巴比妥不同,甲草胺不会导致T4-葡萄糖醛酸化增加和甲状腺激活。

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