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SDZ MRL 953对小鼠的保护作用:抵御活细菌和热灭活细菌引起的死亡

Protection of mice from mortality caused by living and heat-killed bacteria by SDZ MRL 953.

作者信息

Schütze E, Hildebrandt J, Liehl E, Lam C

机构信息

Sandoz Forschungsinstitut, Vienna, Austria.

出版信息

Circ Shock. 1994 Mar;42(3):121-7.

PMID:8025976
Abstract

Protective effects of SDZ MRL 953, a monosaccharidic lipid A analog with a reduced toxicity, were investigated in models of experimental septic shock caused by injections of LPS, and inoculations of heat-killed or live bacteria. Female B6D2F1 mice were challenged with a combination of galactosamine (800 mg/kg) plus various doses of heat-killed isolates of Escherichia coli, Pseudomonas aeruginosa, Salmonella typhimurium, and Staphylococcus aureus or LPS from Salmonella abortus equi. In some experiments, isolates of living bacteria at sublethal inocula were also combined with galactosamine. More than 90% of the animals died within 24 hr when the challenge was performed either simultaneously with or up to 4 hr after an intraperitoneal administration of galactosamine. No death was observed when galactosamine was omitted or administered after the microbial or LPS challenge. Pretreatment of the animals with SDZ MRL 953 (1-10 mg/kg) rendered the animals resistant to the lethal effects of both bacterial and LPS challenge in a time- and dose-dependent manner. The levels of TNF-alpha in control mice rose to greater than 600 pg/ml 2 hr postbacterial or LPS challenge, but were below detection in animals pretreated with SDZ MRL 953. Protection against both the infection and the toxicity of heat-killed bacteria or LPS was also achieved when murine anti-TNF-alpha monoclonal antibody was administered prophylactically. Together, these data suggest that SDZ MRL 953 enhances the resistance of mice against the toxicity of heat-killed gram-negative bacteria and S. aureus, and attenuates host responses to living bacteria which may lead to irreversible shock and death.

摘要

研究了毒性降低的单糖脂质A类似物SDZ MRL 953在注射脂多糖(LPS)以及接种热灭活或活细菌所致实验性脓毒性休克模型中的保护作用。用氨基半乳糖(800 mg/kg)联合不同剂量的热灭活大肠杆菌、铜绿假单胞菌、鼠伤寒沙门氏菌、金黄色葡萄球菌分离株或马流产沙门氏菌的LPS对雌性B6D2F1小鼠进行攻击。在一些实验中,亚致死接种量的活细菌分离株也与氨基半乳糖联合使用。当在腹腔注射氨基半乳糖的同时或之后4小时内进行攻击时,超过90%的动物在24小时内死亡。当省略氨基半乳糖或在微生物或LPS攻击后给药时,未观察到死亡。用SDZ MRL 953(1 - 10 mg/kg)预处理动物,使其对细菌和LPS攻击的致死作用产生时间和剂量依赖性的抗性。对照小鼠在细菌或LPS攻击后2小时,肿瘤坏死因子-α(TNF-α)水平升至大于600 pg/ml,但在用SDZ MRL 953预处理的动物中低于检测水平。当预防性给予鼠抗TNF-α单克隆抗体时,也能预防热灭活细菌或LPS的感染和毒性。总之,这些数据表明SDZ MRL 953增强了小鼠对热灭活革兰氏阴性菌和金黄色葡萄球菌毒性的抗性,并减弱了宿主对活细菌的反应,而这种反应可能导致不可逆的休克和死亡。

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