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格尔德霉素和沙利度胺对手术创伤小鼠Th1/Th2细胞因子平衡的影响。

Effects of geldanamycin and thalidomide on the Th1/Th2 cytokine balance in mice subjected to operative trauma.

作者信息

Nakano Takumi, Araki Keijiro, Nakatani Hajime, Kobayashi Michiya, Sugimoto Takeki, Furuya Yasuo, Matsuoka Takanori, Jin Toufeng, Hanazaki Kazuhiro

机构信息

Department of Tumor Surgery, Kochi Medical School, Kochi University, Nankoku, Japan.

出版信息

Surgery. 2007 Apr;141(4):490-500. doi: 10.1016/j.surg.2006.10.003. Epub 2007 Jan 4.

Abstract

BACKGROUND

Persistence of postoperative immune dysfunction is a critical problem because it increases the risk of serious infectious complications. The mechanisms of the immune dysfunction that occur initially after non-thermal operative injury remain to be fully elucidated.

METHODS

Two mouse models of operative trauma (simple laparotomy to represent minor operative injury and ileocecal resection to represent major operative injury) were used to define the characteristics of initial cytokine synthesis. Geldanamycin and thalidomide were independently added intraperitoneally before and after operative injury to examine the effect on postoperative immune dysfunction. Mice were sacrificed at scheduled times (3, 6, 12, and 24 h after operative injury) and TNF-alpha, IL-2, IL-4, and IL-10 were analyzed. Spleen was used for intracellular cytokines and RT-PCR. Sera were used for ELISA.

RESULTS

Major operative injury caused an initial upregulation of IL-10 synthesis with delayed synthesis of TNF-alpha and IL-2. Minor operative injury caused an early induction of IL-2 synthesis preceded by an initial induction of IL-4 synthesis. GA caused a specific early upregulation of TNF-alpha mRNA expression and intracellular TNF-alpha synthesis. The GA and THD groups showed early serum IL-2 production with reduction of IL-10 mRNA expression and intracellular IL-10 synthesis in the early post-operative phase.

CONCLUSIONS

Major and minor operative injury showed different Th1/Th2 cytokine patterns in the initial post-operative period. Geldanamycin and thalidomide improved the Th1/Th2 imbalance independently after major operative injury.

摘要

背景

术后免疫功能障碍的持续存在是一个关键问题,因为它会增加严重感染并发症的风险。非热手术损伤后最初出现的免疫功能障碍机制仍有待充分阐明。

方法

使用两种手术创伤小鼠模型(简单剖腹术代表轻微手术损伤,回盲部切除术代表严重手术损伤)来确定初始细胞因子合成的特征。在手术损伤前后分别腹腔注射格尔德霉素和沙利度胺,以检查其对术后免疫功能障碍的影响。在预定时间(手术损伤后3、6、12和24小时)处死小鼠,分析肿瘤坏死因子-α(TNF-α)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)和白细胞介素-10(IL-10)。取脾脏用于检测细胞内细胞因子和进行逆转录聚合酶链反应(RT-PCR)。血清用于酶联免疫吸附测定(ELISA)。

结果

严重手术损伤导致IL-10合成最初上调,TNF-α和IL-2合成延迟。轻微手术损伤导致IL-2合成早期诱导,之前是IL-4合成的初始诱导。格尔德霉素导致TNF-α mRNA表达和细胞内TNF-α合成特异性早期上调。格尔德霉素和沙利度胺组在术后早期显示血清IL-2产生增加,IL-10 mRNA表达和细胞内IL-10合成减少。

结论

严重和轻微手术损伤在术后初期表现出不同的Th1/Th2细胞因子模式。格尔德霉素和沙利度胺在严重手术损伤后独立改善了Th1/Th2失衡。

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