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獐牙菜苦苷II通过抑制小鼠炎症反应来预防脓毒症。

Picroside II protects against sepsis via suppressing inflammation in mice.

作者信息

Huang Ying, Zhou Miao, Li Chengbao, Chen Yuanli, Fang Wei, Xu Guo, Shi Xueyin

机构信息

Jiangsu Province Key Laboratory of Anesthesiology and Jiangsu Province Key Laboratory of Anesthesia and Analgesia Application Technology, Xuzhou Medical UniversityXuzhou, China; Department of Anesthesiology and SICU, Xinhua Hospital, School of Medicine, Shanghai Jiaotong UniversityShanghai, China.

Department of Anesthesiology and SICU, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University Shanghai, China.

出版信息

Am J Transl Res. 2016 Dec 15;8(12):5519-5531. eCollection 2016.

Abstract

Picroside II, an iridoid compound extracted from Picrorhiza, exhibits anti-inflammatory and anti-apoptotic activities. We explored the protective effects and mechanisms of picroside II in a mouse model of sepsis induced by cecal ligation and puncture (CLP), using three groups of mice: Group A (sham), Group B (CLP+NS) and Group C (CLP+20 mg/kg picroside II). The mortality in mice with sepsis was decreased by the administration of picroside II, and lung injury was alleviated simultaneously. Picroside II treatment enhanced bacterial clearance in septic mice. Further, picroside II treatment alleviated the inflammatory response in sepsis and enhanced immune function by inhibiting the activation of NLRP3 inflammasome and NF-κB pathways. Picroside II may represent an anti-inflammatory drug candidate, providing novel insight into the treatment of sepsis.

摘要

胡黄连苷II是从胡黄连中提取的一种环烯醚萜类化合物,具有抗炎和抗凋亡活性。我们使用三组小鼠,探索了胡黄连苷II在盲肠结扎穿孔(CLP)诱导的脓毒症小鼠模型中的保护作用及机制:A组(假手术组)、B组(CLP+生理盐水组)和C组(CLP+20mg/kg胡黄连苷II组)。给予胡黄连苷II可降低脓毒症小鼠的死亡率,同时减轻肺损伤。胡黄连苷II治疗可增强脓毒症小鼠的细菌清除能力。此外,胡黄连苷II治疗可减轻脓毒症中的炎症反应,并通过抑制NLRP3炎性小体和NF-κB通路的激活来增强免疫功能。胡黄连苷II可能是一种抗炎候选药物,为脓毒症的治疗提供了新的见解。

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本文引用的文献

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Early Onset Sepsis.
S D Med. 2016 Jan;69(1):29-33.
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NLRP3 inflammasome and its inhibitors: a review.NLRP3炎性小体及其抑制剂:综述
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Molecular mechanisms regulating NLRP3 inflammasome activation.调节NLRP3炎性小体激活的分子机制。
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