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环氧乙烷和1,2-环氧丙烷经口给予大鼠的致癌性。

Carcinogenicity of ethylene oxide and 1,2-propylene oxide upon intragastric administration to rats.

作者信息

Dunkelberg H

出版信息

Br J Cancer. 1982 Dec;46(6):924-33. doi: 10.1038/bjc.1982.303.

Abstract

Ethylene oxide and 1,2-propylene oxide were each administered intragastrically by gavage at 2 dosages (30 and 7.5 mg/kg body wt; 60 and 15 mg/kg body wt respectively) to groups of 50 female Sprague-Dawley rats twice weekly for a period of nearly 3 years using salad oil as the solvent. Both compounds induced local tumours, mainly squamous-cell carcinomas of the forestomach, dependent on the dosage. The first tumour occurred in the 79th week both in the group treated with ethylene oxide and in that treated with 1,2-propylene oxide. The following tumour rates resulted: ethylene oxide 62 and 16%; 1,2-propylene oxide 40 and 4%. In addition carcinomata in situ, papillomas and reactive changes of the squamous epithelium of the forestomach were observed in other animals, but neither ethylene oxide nor 1,2-propylene oxide induced tumours at sites away from the point of administration.

摘要

以色拉油为溶剂,每周两次分别以两种剂量(分别为30和7.5毫克/千克体重;60和15毫克/千克体重)对50只雌性斯普拉格-道利大鼠进行环氧乙烷和1,2-环氧丙烷灌胃,持续近3年。两种化合物均诱发局部肿瘤,主要是前胃鳞状细胞癌,且与剂量有关。第一例肿瘤出现在环氧乙烷处理组和1,2-环氧丙烷处理组的第79周。以下是肿瘤发生率:环氧乙烷为62%和16%;1,2-环氧丙烷为40%和4%。此外,在其他动物中观察到前胃原位癌、乳头状瘤和鳞状上皮的反应性变化,但环氧乙烷和1,2-环氧丙烷均未在给药部位以外的部位诱发肿瘤。

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