首页> 外文期刊>World Journal of Gastroenterology >Changes of inflammation-associated cytokine expressions during early phase of experimental endotoxic shock in macaques
【24h】

Changes of inflammation-associated cytokine expressions during early phase of experimental endotoxic shock in macaques

机译:猕猴内毒素性休克早期炎症相关细胞因子表达的变化

获取原文
获取原文并翻译 | 示例
           

摘要

AIM: To study changes of inflammation-associated cytokine expressions during early phase of endotoxic shock in macague. METHODS: Experiments were performed in Macaque mulatta treated with LPS 2.8 mg/kg in shock model group or with normal saline in control group. Blood samples were collected before, or 60 min, or 120 min after LPS injection, respectively. Liver and spleen tissues were obtained at 120 min after LPS injection. The plasma levels of TNF-α, IL-1 β, IL-10 and IL-12P40 were determined by double-antibody sandwich ELISA with antibodies against human cytokines. The mRNA levels of TNF-α, IL-1 β, and IL-18 in peripheral blood mononuclear cells (PBMCs), liver and spleen were examined by real-time fluorescence semi-quantitative RT-PCR with the primers based on human genes. RESULTS: Mean systemic arterial pressure (MAP), systemic vascular resistance index (SVRI) and left ventricular work index (LVWI) of macaques were significant declined in shock model group on average 60 min after LPS injection. The plasma levels of TNF-α and IL-10 were significantly increased 60 min after LPS injection and then decreased. The plasma levels of IL-1 β and IL-12P40 were significantly increased at 120 min after LPS injection. The mRNA levels of TNF-α and IL-1 β were significantly increased 60 min after LPS stimulation in PBMCs and 120 min after LPS stimulation in livers. The mRNA level of IL-18 was significantly increased 120 min after LPS stimulation in PBMCs and livers. But in spleen, only TNF-α mRNA level in LPS group was significantly higher 120 min after LPS stimulation, compared with that in control group. CONCLUSION: An endotoxic shock model of Macaque mulatta was successfully established. Both antibodies for ELISA and PCR primers based on human cytokine assays were successfully applied to detect macaque cytokines. In the model, inflammatory cytokines, such as TNF-α, IL-1 β, IL-12 and IL-18 as well as anti-inflammation cytokine IL-10, were released at very early phase of endotoxic shock within 120 min after LPS injection. PBMCs and liver cells might be the important sources of these cytokines.
机译:目的:研究马格内毒素休克早期炎症相关细胞因子表达的变化。方法:在休克模型组中,以LPS 2.8 mg / kg的猕猴或对照组中的生理盐水,对猕猴进行实验。在分别注射LPS之前,之后60分钟或120分钟后收集血液样本。 LPS注射后120分钟获得肝和脾组织。通过抗人细胞因子抗体的双抗体夹心ELISA测定血浆TNF-α,IL-1β,IL-10和IL-12P40的水平。使用基于人类基因的引物,通过实时荧光半定量RT-PCR检测外周血单核细胞(PBMC),肝和脾中TNF-α,IL-1β和IL-18的mRNA水平。结果:休克模型组平均注射LPS后60分钟,猕猴的平均全身动脉压(MAP),全身血管阻力指数(SVRI)和左心室工作指数(LVWI)显着下降。 LPS注射后60分钟,血浆TNF-α和IL-10的水平显着升高,然后下降。注射LPS后120分钟时,血浆IL-1β和IL-12P40的水平显着升高。 PBMC中LPS刺激后60分钟和肝脏中LPS刺激后120分钟,TNF-α和IL-1β的mRNA水平显着升高。 LPS刺激后,PBMC和肝脏中IL-18的mRNA水平显着增加120分钟。但是在脾脏中,LPS刺激后120分钟,仅LPS组的TNF-αmRNA水平显着高于对照组。结论:成功建立了猕猴内毒素休克模型。基于人细胞因子测定的ELISA抗体和PCR引物均成功应用于检测猕猴细胞因子。在该模型中,LPS发生后120分钟内毒素休克的非常早期,炎症细胞因子如TNF-α,IL-1β,IL-12和IL-18以及抗炎细胞因子IL-10被释放。注射。 PBMC和肝细胞可能是这些细胞因子的重要来源。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号