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A New Cecal Slurry Preparation Protocol with Improved Long-Term Reproducibility for Animal Models of Sepsis

机译:一种新型的盲肠浆液制备方案可改善脓毒症动物模型的长期再现性

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摘要

Sepsis, a life-threatening systemic inflammatory response syndrome induced by infection, is widely studied using laboratory animal models. While cecal-ligation and puncture (CLP) is considered the gold standard model for sepsis research, it may not be preferable for experiments comparing animals of different size or under different dietary regimens. By comparing cecum size, shape, and cecal content characteristics in mice under different experimental conditions (aging, diabetes, pancreatitis), we show that cecum variability could be problematic for some CLP experiments. The cecal slurry (CS) injection model, in which the cecal contents of a laboratory animal are injected intraperitoneally to other animals, is an alternative method for inducing polymicrobial sepsis; however, the CS must be freshly prepared under conventional protocols, which is a major disadvantage with respect to reproducibility and convenience. The objective of this study was to develop an improved CS preparation protocol that allows for long-term storage of CS with reproducible results. Using our new CS preparation protocol we found that bacterial viability is maintained for at least 6 months when the CS is prepared in 15% glycerol-PBS and stored at -80°C. To test sepsis-inducing efficacy of stored CS stocks, various amounts of CS were injected to young (4–6 months old), middle-aged (12–14 months old), and aged (24–26 months old) male C57BL/6 mice. Dose- and age-dependent mortality was observed with high reproducibility. Circulating bacteria levels strongly correlated with mortality suggesting an infection-mediated death. Further, injection with heat-inactivated CS resulted in acute hypothermia without mortality, indicating that CS-mediated death is not due to endotoxic shock. This new CS preparation protocol results in CS stocks which are durable for freezing preservation without loss of bacterial viability, allowing experiments to be performed more conveniently and with higher reproducibility than before.
机译:脓毒症是一种由感染引起的危及生命的全身性炎症反应综合征,已使用实验室动物模型进行了广泛研究。虽然盲肠结扎和穿刺(CLP)被认为是败血症研究的金标准模型,但对于比较不同大小或不同饮食方案的动物的实验可能不是优选的。通过比较不同实验条件(衰老,糖尿病,胰腺炎)下小鼠的盲肠大小,形状和盲肠含量特征,我们显示盲肠变异性对于某些CLP实验可能是成问题的。盲肠浆液(CS)注射模型是诱导多菌性败血症的另一种方法,其中将实验动物的盲肠内容物腹膜内注射到其他动物中。然而,CS必须在常规方案下新鲜制备,这在可重复性和便利性方面是主要缺点。这项研究的目的是开发一种改进的CS制备方案,该方案允许CS的长期保存并具有可重复的结果。使用我们的新CS制备方案,我们发现,在15%甘油-PBS中制备CS并储存在-80°C时,细菌生存力至少可以维持6个月。为了测试储存的CS菌库对败血症的诱导作用,向C57BL /的年轻(4-6个月大),中年(12-14个月大)和年龄(24-26个月大)分别注射了不同数量的CS。 6只小鼠。观察到剂量和年龄依赖性的死亡率,具有较高的再现性。循环细菌水平与死亡率密切相关,表明感染介导的死亡。此外,注射热灭活的CS会导致急性低温而无死亡,表明CS介导的死亡不是由于内毒素休克引起的。这种新的CS制备方案可生产出CS储备液,该储备液可用于冷冻保存而不会丧失细菌生存力,从而使实验比以前更方便且可重复性更高。

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