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轻度低温通过 TLR4/NF-κB/NLRP3 信号通路减轻 CLP 诱导的多器官功能障碍减轻细胞焦亡。

Mild Hypothermia Alleviates CLP-induced Multiple Organ Dysfunction by Mitigating Pyroptosis Through the TLR4/NF-κB/NLRP3 Signaling Pathway.

机构信息

Intensive Care Unit, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Intensive Care Unit, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

Arch Med Res. 2023 Jan;54(1):7-16. doi: 10.1016/j.arcmed.2022.11.005. Epub 2022 Dec 30.

Abstract

BACKGROUND

Multiple organ failure secondary to severe sepsis leads to increased morbidity and mortality and is often accompanied by inflammation and immune system dysfunction. Mild hypothermia has been shown to have anti-inflammatory properties, but whether it can exert a protective effect in cases of multiple organ failure remains unclear. Thus, in this study, we investigated the protective effect of mild hypothermia on septic multiple organ failure and the underlying mechanism for this effect.

METHOD

Sepsis was induced through the cecal ligation and puncture (CLP) method. Rats were then housed at normal (36-38°C) or mild hypothermic (32-34°C) temperature for 10 h.

RESULTS

CLP-induced effects on inflammatory cytokines and biochemical markers in serum were reversed by mild hypothermia. The pathological injury score and the expressions of pyroptosis markers, including TLR4, MyD88 and NF-κB signaling molecules, showed a similar trend. Moreover, 3 d survival of CLP rats was improved by mild hypothermia.

CONCLUSIONS

Mild hypothermia alleviated CLP-induced organ failure and the downstream effects on pyroptosis, probably through the TLR4/NF-κB/NLRP3 signaling pathway.

摘要

背景

严重脓毒症导致的多器官衰竭会增加发病率和死亡率,常伴有炎症和免疫系统功能障碍。轻度低温已被证明具有抗炎作用,但它是否能在多器官衰竭的情况下发挥保护作用尚不清楚。因此,在这项研究中,我们研究了轻度低温对脓毒症多器官衰竭的保护作用及其作用机制。

方法

通过盲肠结扎穿孔(CLP)法诱导脓毒症。然后,将大鼠在正常(36-38°C)或轻度低温(32-34°C)下饲养 10 小时。

结果

轻度低温逆转了 CLP 诱导的血清中炎症细胞因子和生化标志物的变化。病理损伤评分和细胞焦亡标志物(包括 TLR4、MyD88 和 NF-κB 信号分子)的表达也呈现出相似的趋势。此外,轻度低温可提高 CLP 大鼠的 3 天存活率。

结论

轻度低温缓解了 CLP 诱导的器官衰竭及下游的细胞焦亡效应,可能是通过 TLR4/NF-κB/NLRP3 信号通路。

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