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苯甲醇与细菌内毒素的毒性相互作用。

Toxic interactions of benzyl alcohol with bacterial endotoxin.

作者信息

Cebula T A, El-Hage A N, Ferrans V J

出版信息

Infect Immun. 1984 Apr;44(1):91-6. doi: 10.1128/iai.44.1.91-96.1984.

Abstract

Acute toxic interactions of intravenously administered benzyl alcohol and Escherichia coli O55:B5 (Boivin preparation) endotoxin were examined in rodents. Lethality studies in male CD-1 mice demonstrated that these agents were more toxic when administered in combination than when either was administered alone. Prophylactic treatment with diazepam (5 mg/kg intraperitoneally) protected against lethality induced by either the combination or the endotoxin yet offered little, if any, protection against the lethal effects of benzyl alcohol. Similar treatments with naloxone (5 mg/kg intraperitoneally) failed to protect against either endotoxin-induced or benzyl alcohol-induced lethality, but they significantly protected against the lethal effects of the combination. Although hexobarbital-induced sleeping time was prolonged in endotoxin-treated mice (but was normal in benzyl alcohol-treated mice), a more protracted effect on sleeping time was observed in mice treated with both benzyl alcohol and endotoxin. Moreover, male Wistar rats treated with benzyl alcohol (40 mg) showed no evidence of hepatic lesions, but rats treated in combination with sublethal doses of the alcohol (40 mg) and the endotoxin (0.4 mg) developed hepatic lesions which were severe than those observed in rats treated with endotoxin (0.4 mg) alone. A correlation between altered blood chemistry values and severity of hepatic lesions was demonstrated. These data show in vivo toxic interactions between benzyl alcohol and bacterial endotoxin. In addition, our results indicate that the toxic effects induced by the benzyl alcohol-endotoxin combination are due to an enhancement of the lethal properties of bacterial endotoxin.

摘要

在啮齿动物中研究了静脉注射苯甲醇与大肠杆菌O55:B5(博伊文制剂)内毒素的急性毒性相互作用。对雄性CD-1小鼠的致死性研究表明,这些药物联合使用时比单独使用时毒性更大。地西泮(5mg/kg腹腔注射)预防性治疗可预防联合用药或内毒素诱导的致死性,但对苯甲醇的致死作用几乎没有保护作用(如果有保护作用的话也很小)。用纳洛酮(5mg/kg腹腔注射)进行类似治疗不能预防内毒素或苯甲醇诱导的致死性,但能显著预防联合用药的致死作用。虽然在内毒素处理的小鼠中戊巴比妥诱导的睡眠时间延长(但在苯甲醇处理的小鼠中正常),但在同时用苯甲醇和内毒素处理的小鼠中观察到对睡眠时间有更持久的影响。此外,用苯甲醇(40mg)处理的雄性Wistar大鼠没有肝损伤的迹象,但用亚致死剂量的酒精(40mg)和内毒素(0.4mg)联合处理的大鼠出现了比单独用内毒素(0.4mg)处理的大鼠更严重的肝损伤。血液化学值的改变与肝损伤的严重程度之间存在相关性。这些数据表明苯甲醇与细菌内毒素之间存在体内毒性相互作用。此外,我们的结果表明,苯甲醇-内毒素联合诱导的毒性作用是由于细菌内毒素致死特性的增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b005/263474/c6509ca84c63/iai00127-0102-a.jpg

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