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氯丙嗪在体内对白细胞介素-1和肿瘤坏死因子介导的活性具有保护作用。

Chlorpromazine protection against interleukin-1 and tumor necrosis factor-mediated activities in vivo.

作者信息

Bertini R, Mengozzi M, Bianchi M, Sipe J D, Ghezzi P

机构信息

Istituto di Richerche Farmacologiche Mario Negri, Milano, Italy.

出版信息

Int J Immunopharmacol. 1991;13(8):1085-90. doi: 10.1016/0192-0561(91)90159-5.

Abstract

Interleukin (IL-1) and tumor necrosis factor (TNF) are thought to play a key role in septic shock and inflammation. We had previously shown that chlorpromazine (CPZ) has a protective effect in various models of endotoxic shock and IL-1 toxicity. We have tested the effect of CPZ on several activities of IL-1 in vivo. CPZ (4 mg/kg) inhibited increases in serum corticosterone, triglycerides and serum amyloid A (SAA). Chlorpromazine also antagonized these same effects when they were induced by endotoxin or TNF, suggesting that this activity could be implicated in the protective effect of CPZ in various models of endotoxic shock and IL-1 lethality.

摘要

白细胞介素(IL-1)和肿瘤坏死因子(TNF)被认为在脓毒性休克和炎症中起关键作用。我们之前已经表明,氯丙嗪(CPZ)在各种内毒素休克和IL-1毒性模型中具有保护作用。我们已经在体内测试了CPZ对IL-1多种活性的影响。CPZ(4毫克/千克)抑制了血清皮质酮、甘油三酯和血清淀粉样蛋白A(SAA)的升高。当这些效应由内毒素或TNF诱导时,氯丙嗪也能拮抗这些相同的效应,这表明这种活性可能与CPZ在各种内毒素休克模型和IL-1致死性中的保护作用有关。

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