Hollinger M A
J Pharmacol Exp Ther. 1984 Aug;230(2):292-4.
Mice treated with Escherichia coli endotoxin (500 micrograms/kg i.p.) 24 and 1 hr before paraquat dichloride (50 mg/kg i.p.) had a 2-fold increase in 7-day cumulative mortality compared to those injected with buffered saline before paraquat. The duration of the prior exposure time to endotoxin appears to be an important determinant of the potentiating effect as more mice died after 24 than 1 hr pretreatment. The potentiating effect of endotoxin on paraquat-induced lethality is not due to increased uptake of the toxicant. Lung values of radioactivity from [14C]paraquat were not significantly different between endotoxin and buffered saline-treated mice. Despite the potentiating effect of endotoxin on paraquat-induced lethality, it appears that the lipopolysaccharide is able to provide some protection to the pulmonary capillary endothelium because pretreatment reverses an increase in serum angiotensin converting enzyme. Although not addressed in the present investigation, possible mechanisms for the potentiating effect of endotoxin on paraquat-induced lethality may involve superoxide anion generation, superoxide dismutase inhibition or both.
在用百草枯二氯化物(腹腔注射50毫克/千克)前24小时和1小时腹腔注射大肠杆菌内毒素(500微克/千克)的小鼠,与在用百草枯前注射缓冲盐水的小鼠相比,7天累积死亡率增加了2倍。内毒素先前暴露时间的长短似乎是增强作用的一个重要决定因素,因为与1小时预处理相比,24小时预处理后更多的小鼠死亡。内毒素对百草枯诱导的致死率的增强作用并非由于毒物摄取增加。内毒素处理组和缓冲盐水处理组小鼠的[14C]百草枯肺放射性值无显著差异。尽管内毒素对百草枯诱导的致死率有增强作用,但脂多糖似乎能够为肺毛细血管内皮提供一定保护,因为预处理可逆转血清血管紧张素转换酶的升高。尽管本研究未涉及,但内毒素对百草枯诱导的致死率增强作用的可能机制可能涉及超氧阴离子生成、超氧化物歧化酶抑制或两者兼有。