Bertini R, Bianchi M, Mengozzi M, Ghezzi P
Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Biochem Biophys Res Commun. 1989 Dec 29;165(3):942-6. doi: 10.1016/0006-291x(89)92694-6.
Interleukin 1 (IL-1) and Tumor Necrosis Factor (TNF) are thought to play a key role in septic shock and inflammation. We have tested the effect of dexamethasone (DEX) and chlorpromazine (CPZ) on the lethal effect of IL-1, TNF and endotoxin. Two different experimental models were used to sensitize mice to the lethal effect of IL-1: adrenalectomy and pretreatment with actinomycin D. CPZ (4 mg/kg) was found to protect mice against IL-1 and endotoxin toxicity in all cases, while DEX had a protective effect only in adrenalectomized mice. In contrast to its protective effect against IL-1 and endotoxin, CPZ did not protect mice against TNF. These findings might be useful in the analysis of the differences in the actions of IL-1 and TNF in vivo, and in the development of new drugs preventing their toxicity.
白细胞介素1(IL-1)和肿瘤坏死因子(TNF)被认为在脓毒症休克和炎症中起关键作用。我们测试了地塞米松(DEX)和氯丙嗪(CPZ)对IL-1、TNF和内毒素致死作用的影响。使用两种不同的实验模型使小鼠对IL-1的致死作用敏感:肾上腺切除术和用放线菌素D预处理。发现在所有情况下CPZ(4毫克/千克)都能保护小鼠免受IL-1和内毒素毒性的影响,而DEX仅在肾上腺切除的小鼠中具有保护作用。与它对IL-1和内毒素的保护作用相反,CPZ不能保护小鼠免受TNF的影响。这些发现可能有助于分析IL-1和TNF在体内作用的差异,以及开发预防它们毒性的新药。