Pickett W C, Torley L W, Dejoy S Q, Gibbons J J, Desai N R, Oronsky A L, Kerwar S S
Oncology, Immunology, and Formulations Research Section, American Cyanamid, Lederle Laboratories, Pearl River, NY 10965.
Crit Care Med. 1992 Oct;20(10):1448-53. doi: 10.1097/00003246-199210000-00014.
In murine models of endotoxemia, large amounts of lipopolysaccharide have to be administered to induce mortality. If mice are pretreated with D-galactosamine, the amount of lipopolysaccharide required to induce mortality is significantly lowered. Pluronic F 127 liquid is a relatively non-toxic copolymer that exhibits reverse gelation properties. Thus, it is a liquid at cold temperature and a gel at body temperature. The present studies were performed to ascertain whether the reverse gelation properties of Pluronic F 127 liquid could be used in devising a model of septic shock where a sustained delivery of lipopolysaccharide occurred. In evaluating this model, dose-response studies were conducted with lipopolysaccharide when a) it was administered intraperitoneally in saline or in Pluronic F 127 liquid, and b) it was administered intravenously to mice that had been pretreated with saline or Pluronic F 127 liquid. Mortality was followed for up to 72 hrs.
Various doses of Escherichia coli lipopolysaccharide dissolved in saline or in Pluronic F 127 liquid were administered intraperitoneally to mice. The lethal dose of lipopolysaccharide required to kill 50% of the mice (LD50) administered in Pluronic F 127 liquid was approximately ten- to 15-fold less than the values obtained for lipopolysaccharide administered in saline. This decrease in the LD50 of lipopolysaccharide was also observed if the mice were treated intraperitoneally with Pluronic F 127 liquid and challenged 6 hrs later with iv lipopolysaccharide. The concentrations of tumor necrosis factor and interleukin-6 in the plasma were significantly higher when a low dose of lipopolysaccharide was administered to mice that had been pretreated with Pluronic F 127 liquid. While there was no effect on the liver enzymes, Pluronic F 127 liquid caused an increase in the plasma triglycerides.
The data reported in this paper indicate that the LD50 of lipopolysaccharide is significantly decreased if it is administered in Pluronic F 127 liquid or administered to mice that have been pretreated with the Pluronic F 127 liquid. Thus, Pluronic F 127 liquid appears to sensitize mice to low levels of lipopolysaccharide. Unlike the D-galactosamine model, lipopolysaccharide can be administered as late as 6 hrs after treatment with Pluronic F 127 liquid. While the mechanisms by which Pluronic F 127 liquid sensitizes mice is not known, plasma triglycerides were increased in mice treated with this agent, suggesting that tissues responsible for the synthesis and/or degradation of triglycerides play a role in this sensitization process.
在内毒素血症的小鼠模型中,必须给予大量脂多糖才能诱导死亡。如果小鼠预先用D - 半乳糖胺处理,诱导死亡所需的脂多糖量会显著降低。普朗尼克F127液体是一种相对无毒的共聚物,具有逆凝胶化特性。因此,它在低温下是液体,在体温下是凝胶。本研究旨在确定普朗尼克F127液体的逆凝胶化特性是否可用于设计一种脓毒症休克模型,使脂多糖能够持续释放。在评估该模型时,当脂多糖:a)腹腔注射于生理盐水或普朗尼克F127液体中,以及b)静脉注射于预先用生理盐水或普朗尼克F127液体处理过的小鼠时,进行了剂量反应研究。观察死亡率长达72小时。
将不同剂量溶于生理盐水或普朗尼克F127液体中的大肠杆菌脂多糖腹腔注射给小鼠。普朗尼克F127液体中注射的脂多糖杀死50%小鼠所需的致死剂量(LD50)比生理盐水注射的脂多糖值低约10至15倍。如果小鼠腹腔注射普朗尼克F127液体并在6小时后静脉注射脂多糖进行攻击,也观察到脂多糖LD50的这种降低。当给预先用普朗尼克F127液体处理过的小鼠注射低剂量脂多糖时,血浆中肿瘤坏死因子和白细胞介素-6的浓度显著更高。虽然对肝酶没有影响,但普朗尼克F127液体导致血浆甘油三酯升高。
本文报道的数据表明,如果脂多糖在普朗尼克F127液体中给药或给预先用普朗尼克F127液体处理过的小鼠给药,其LD50会显著降低。因此,普朗尼克F127液体似乎使小鼠对低水平脂多糖敏感。与D - 半乳糖胺模型不同,脂多糖可在普朗尼克F127液体处理后6小时给药。虽然普朗尼克F127液体使小鼠敏感的机制尚不清楚,但用该制剂处理的小鼠血浆甘油三酯升高,表明负责甘油三酯合成和/或降解的组织在这种敏感化过程中起作用。