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吡咯烷二硫代氨基甲酸盐可增强白细胞介素-10的生成,抑制肿瘤坏死因子-α、巨噬细胞炎性蛋白-1α、白细胞介素-12的生成以及一氧化氮的产生,并可对内毒素的致死效应起到保护作用。

Pyrrolidine dithiocarbamate augments IL-10, inhibits TNF-alpha, MIP-1alpha, IL-12, and nitric oxide production and protects from the lethal effect of endotoxin.

作者信息

Németh Z H, Haskó G, Vizi E S

机构信息

Department of Pharmacology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest.

出版信息

Shock. 1998 Jul;10(1):49-53. doi: 10.1097/00024382-199807000-00009.

Abstract

During endotoxemia, immune cells activated by lipopolysaccharide (LPS) produce various inflammatory mediators, including cytokines and nitric oxide (NO). The genes of several mediators are activated in part by the rapid binding of the transcription factor nuclear factor-kappa B (NF-kappaB) to its promoter. The induction of this transcription factor can be blocked by a wide range of antioxidants, including pyrrolidine dithiocarbamate (PDTC). Here we investigated in mice the effect of this compound on the plasma tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma), interleukin-1alpha (IL-1alpha), interleukin-6 (IL-6), interleukin-10 (IL-10), interleukin-12 (IL-12), macrophage inflammatory protein-1alpha (MIP-1alpha), and nitric oxide (NO) response to intraperitoneal (i.p.) injection of LPS. Pretreatment of animals with PDTC (10-100 mg/kg) 30 min prior to LPS challenge (4 mg/kg, i.p.) decreased plasma TNF-alpha, IL-12, MIP-1alpha, and nitrite/nitrate (breakdown products of NO) concentrations, but enhanced plasma levels of IL-10. Moreover, pretreatment of mice with PDTC (10-100 mg/kg, i.p.) did not alter LPS-induced (4 mg/kg) production of IL-1alpha, IL-6, and IFN-gamma. Finally, PDTC (100 mg/kg) protected the mice against LPS (100 mg/kg)-induced lethality. These results indicate that blockade of the NF-kappaB pathway by PDTC has potent anti-inflammatory action in systemic inflammatory processes.

摘要

在内毒素血症期间,被脂多糖(LPS)激活的免疫细胞会产生多种炎症介质,包括细胞因子和一氧化氮(NO)。几种介质的基因部分是通过转录因子核因子-κB(NF-κB)与其启动子的快速结合而被激活的。包括吡咯烷二硫代氨基甲酸盐(PDTC)在内的多种抗氧化剂可阻断这种转录因子的诱导。在此,我们在小鼠中研究了该化合物对腹腔注射(i.p.)LPS后血浆肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)、白细胞介素-1α(IL-1α)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、白细胞介素-12(IL-12)、巨噬细胞炎性蛋白-1α(MIP-1α)和一氧化氮(NO)反应的影响。在LPS攻击(4mg/kg,i.p.)前30分钟用PDTC(10-100mg/kg)对动物进行预处理,可降低血浆TNF-α、IL-12、MIP-1α和亚硝酸盐/硝酸盐(NO的分解产物)浓度,但可提高血浆IL-10水平。此外,用PDTC(10-100mg/kg,i.p.)对小鼠进行预处理不会改变LPS诱导(4mg/kg)的IL-1α、IL-6和IFN-γ的产生。最后,PDTC(100mg/kg)可保护小鼠免受LPS(100mg/kg)诱导的致死作用。这些结果表明,PDTC对NF-κB途径的阻断在全身炎症过程中具有强大的抗炎作用。

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