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肉桂精油对内毒素中毒小鼠的保护作用。

Protective effects of essential oils from Rimulus cinnamon on endotoxin poisoning mice.

机构信息

Department of Pharmacology, College of Pharmacy, Chengdu University of TCM, Wenjiang District, Chengdu, Sichuan Province, 611137, PR China.

Department of Pharmacology, College of Pharmacy, Chengdu University of TCM, Wenjiang District, Chengdu, Sichuan Province, 611137, PR China.

出版信息

Biomed Pharmacother. 2018 May;101:304-310. doi: 10.1016/j.biopha.2018.02.092. Epub 2018 Mar 22.

Abstract

The essential oils from Rimulus cinnamon (EORC) have anti-inflammation activities, but the effects of EORC on endotoxin poisoning mice remain to be explored, the mechanism is still unclear. This study was designed to investigate the protective effects and mechanism of EORC on lipopolysaccharide (LPS)-induced endotoxin poisoning mice. Pre-treatment with EORC decreased the production of pro-inflammatory cytokines (Interleukin-1β, Interleukin-18, Interleukin-5, and Interferon-γ) and chemokines (Monocyte chemotactic protein-1, Macrophage colony-stimulating factor, and Macrophage inflammatory protein-1β) in serum of endotoxin poisoning mice. The histopathological study showed that the lung injury was improved and EORC decreased the numbers of neutrophils and Nitric oxide (NO) levels in lung. EORC could reduce the mRNA expression of NLR family, pyrin domain-containing 3 (NLRP3), Interleukin (IL)-1β, and nitric oxide synthase (iNOS). In addition, EORC decreased the protein expression of NLRP3, Caspase-1 (p20), Pro-IL-1β, and purinergic P2 × 7 receptor (P2 × 7R) in the lung tissues. The results above indicated that the EORC may have protective effects on LPS-induced endotoxin poisoning mice via inhibiting the activation of P2 × 7R/NLRP3 inflammasome.

摘要

灵香草精油(EORC)具有抗炎活性,但 EORC 对内毒素中毒小鼠的作用仍有待探索,其机制尚不清楚。本研究旨在探讨 EORC 对内毒素中毒小鼠的保护作用及其机制。EORC 预处理可降低内毒素中毒小鼠血清中促炎细胞因子(白细胞介素-1β、白细胞介素-18、白细胞介素-5 和干扰素-γ)和趋化因子(单核细胞趋化蛋白-1、巨噬细胞集落刺激因子和巨噬细胞炎症蛋白-1β)的产生。组织病理学研究表明,EORC 可改善肺损伤并降低肺内中性粒细胞数量和一氧化氮(NO)水平。EORC 可降低 NLR 家族、pyrin 结构域包含蛋白 3(NLRP3)、白细胞介素(IL)-1β 和一氧化氮合酶(iNOS)的 mRNA 表达。此外,EORC 可降低肺组织中 NLRP3、Caspase-1(p20)、Pro-IL-1β 和嘌呤能 P2×7 受体(P2×7R)的蛋白表达。上述结果表明,EORC 可能通过抑制 P2×7R/NLRP3 炎性小体的激活对 LPS 诱导的内毒素中毒小鼠发挥保护作用。

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