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[吸入二异氰酸酯暴露诱导大鼠肝脏病灶]

[Induction of rat liver foci by inhaled diisocyanate exposure].

作者信息

Wiethege T, Potthast J, Marczynski B, Marek W, Voss B, Baur X

机构信息

Berufsgenossenschaftliches Forschungsinstitut für Arbeitsmedizin, Institut an der Ruhr-Universität Bochum.

出版信息

Pneumologie. 1995 Jun;49(6):373-7.

PMID:7644458
Abstract

Diisocyanates are increasingly used for manufacturing polyurethane foam, elastomers, adhesives, coatings, insecticides and many other products. The large number of workers being exposed to these chemicals has a concentration-dependent risk of developing chronic airway disorders. The clinical role of genotoxic effects of diisocyanates demonstrable in vivo and in vitro is still unclear just as their possible cancerogenic potential. The possible initiating effect of diisocyanates in liver carcinogenesis was studied using a rat liver foci bioassay (RFLA). The RLFA is based on the histochemical demonstration of foci of hepatocytes with altered enzyme equipment, which are induced by carcinogens. These foci are generally regarded as early preneoplastic lesions. Rats were exposed either to 20 ppb TDI (Toluene diisocyanate) or 20 ppb HDI (Hexamethylene diisocyanate) for two hours a day over a period of four weeks. After a break of one week the rats received 10 mg Clophen A50/kg body weight as promotor for possible isocyanate induced tumorigenic lesions twice a week for eight weeks. For positive control the hepatocarcinogen diethylnitrosamin (DEN) was given as a single dose of 10 mg and 20 mg. All animals were sacrificed aged 16 weeks. Serial cryostat sections were prepared for ATPase and gamma GT staining. The foci number was determined and calculated as foci/animal as a mean value taken from both staining protocols. Preneoplastic liver foci were observed in positive control rats treated with a single dose of 10 mg as well as with 20 mg DEN (4.3 +/- 3.2 and 1.8 +/- 1.4 respectively). In none of the animals exposed to TDI or HDI preneoplastic foci were detectable.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

二异氰酸酯越来越多地用于制造聚氨酯泡沫、弹性体、粘合剂、涂料、杀虫剂和许多其他产品。大量接触这些化学物质的工人有患慢性气道疾病的浓度依赖性风险。二异氰酸酯在体内和体外可证实的遗传毒性作用的临床作用,以及它们可能的致癌潜力仍不清楚。使用大鼠肝灶生物测定法(RFLA)研究了二异氰酸酯在肝癌发生中的可能起始作用。RFLA基于对具有改变的酶设备的肝细胞灶的组织化学显示,这些灶是由致癌物诱导的。这些灶通常被视为早期癌前病变。大鼠每天暴露于20 ppb甲苯二异氰酸酯(TDI)或20 ppb六亚甲基二异氰酸酯(HDI)中,持续四周,每天两小时。休息一周后,大鼠每周两次接受10 mg氯芬A50/kg体重作为可能由异氰酸酯诱导的致瘤性病变的促进剂,持续八周。作为阳性对照,给予肝癌致癌物二乙基亚硝胺(DEN)单次剂量10 mg和20 mg。所有动物在16周龄时处死。制备连续的冰冻切片用于ATP酶和γ-谷氨酰转移酶染色。确定灶的数量并计算为每只动物的灶数,作为取自两种染色方案的平均值。在接受单次剂量10 mg和20 mg DEN治疗的阳性对照大鼠中观察到癌前肝灶(分别为4.3±3.2和1.8±1.4)。在暴露于TDI或HDI的动物中均未检测到癌前灶。(摘要截断于250字)

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