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甲巯咪唑在嗅鼻黏膜中的代谢依赖性毒性。

Metabolism-dependent toxicity of methimazole in the olfactory nasal mucosa.

作者信息

Brittebo E B

机构信息

Department of Pharmacology, University of Lund, Sweden.

出版信息

Pharmacol Toxicol. 1995 Jan;76(1):76-9. doi: 10.1111/j.1600-0773.1995.tb00107.x.

Abstract

In mice given a single intraperitoneal injection of the antithyroid drug methimazole (0.44 mmol/kg; 50 mg/kg) detachment of the olfactory neuroepithelium and necrosis of the Bowman's glands in the lamina propria was observed 24 hr after administration. Three days after administration there was an atypical epithelium throughout the olfactory region and the Bowman's glands had disappeared. Pretreatment with the olfactory cytochrome P450 inhibitor metyrapone protected against the methimazole-induced changes at this site. In mice injected with the methimazole analogues 1-methylimidazole or 4-methylimidazole (0.44 mmol/kg; 36 mg/kg) or the antithyroid drug propylthiuracil (0.22 mmol/kg; 38 mg/kg) no morphological changes were observed in the olfactory mucosa. The results suggest that methimazole-induced toxicity in the olfactory mucosa is related to metabolism-dependent changes of the thiol group.

摘要

给小鼠腹腔注射一次抗甲状腺药物甲巯咪唑(0.44毫摩尔/千克;50毫克/千克)后,给药24小时观察到嗅神经上皮脱离和固有层中鲍曼腺坏死。给药三天后,整个嗅觉区域出现非典型上皮,鲍曼腺消失。用嗅觉细胞色素P450抑制剂美替拉酮预处理可防止该部位由甲巯咪唑诱导的变化。给小鼠注射甲巯咪唑类似物1-甲基咪唑或4-甲基咪唑(0.44毫摩尔/千克;36毫克/千克)或抗甲状腺药物丙硫氧嘧啶(0.22毫摩尔/千克;38毫克/千克)后,嗅黏膜未观察到形态学变化。结果表明,甲巯咪唑诱导的嗅黏膜毒性与硫醇基团的代谢依赖性变化有关。

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