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侧柏叶的亚甲基氯仿部分通过阻断 NF-κB 和 p38 MAPK 信号通路抑制体外炎症生物标志物,并保护小鼠免受致死性内毒素血症的影响。

Methylene chloride fraction of the leaves of Thuja orientalis inhibits in vitro inflammatory biomarkers by blocking NF-κB and p38 MAPK signaling and protects mice from lethal endotoxemia.

机构信息

Department of Oriental Pathology, College of Oriental Medicine and Institute of Oriental Medicine, Kyung Hee University, 1 Hoegidong Dongdaemungu, Seoul 130-701, Republic of Korea.

出版信息

J Ethnopharmacol. 2011 Jan 27;133(2):687-95. doi: 10.1016/j.jep.2010.10.051. Epub 2010 Oct 30.

Abstract

AIM OF THE STUDY

Thuja orientalis (TO) has been a recognized herbal medicine across Northeast Asian countries for thousands of years and used for the treatment of various inflammatory diseases through as yet undefined mechanisms. In this study, we set out to determine whether the anti-inflammatory effects of this plant are mediated to suppress mitogen-activated protein kinases (MAPKs) and nuclear factor-κB (NF-κB) activation in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells.

MATERIALS AND METHODS

RAW 264.7 cells were pretreated with the methylene chloride fraction of TO (MTO) and stimulated with LPS. Nitric oxide (NO) release was determined by the accumulation of nitrite in the culture supernatants and tumor necrosis factor-α (TNF-α) and IL-6 secretion were determined by immunoenzymatic assay. Inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression were evaluated via RT-PCR and Western blotting. NF-κB activation was also evaluated by reporter gene assay and electrophoretic mobility shift assay (EMSA). In addition, the protective effect of MTO was evaluated by use of the LPS-induced endotoxin shock model in mice.

RESULTS

We found that MTO significantly suppressed LPS-stimulated NO and IL-6 production without affecting cell viability. MTO inhibited the expression of LPS-induced iNOS and COX-2 protein and their mRNA expression. Also, TNF-α and IL-6 secretion were decreased by MTO in both PMA and ionomycin-stimulated splenocytes. As a result, MTO inhibited pro-inflammatory cytokines such as TNF-α and IL-6, which is hypothesized as being due to the suppression of LPS-induced p38 MAPK and NF-κB activation. Moreover, MTO improved the survival rate during lethal endotoxemia by inhibiting the production of TNF-α in an animal model and our LC-MS analysis showed that a major component of MTO was pinusolide.

CONCLUSIONS

We demonstrate here the evidence that the methylene chloride fraction of Thuja orientalis (MTO) potentially inhibits the biomarkers related to inflammation in vitro and in vivo, and might be provided as a potential candidate for the treatment of inflammatory diseases.

摘要

研究目的

东方杉(TO)作为一种被东北亚国家认可的草药,已有数千年的历史,用于治疗各种炎症性疾病,但具体机制尚不清楚。在本研究中,我们旨在确定该植物的抗炎作用是否通过抑制丝裂原活化蛋白激酶(MAPK)和核因子-κB(NF-κB)的激活来实现,方法是用脂多糖(LPS)刺激 RAW 264.7 细胞。

材料和方法

用 TO 的二氯甲烷部分(MTO)预处理 RAW 264.7 细胞,然后用 LPS 刺激。通过测定培养上清液中亚硝酸盐的积累来确定一氧化氮(NO)的释放,通过免疫酶测定法来测定肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的分泌。通过 RT-PCR 和 Western blot 评估诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达。还通过报告基因测定和电泳迁移率变动分析(EMSA)评估 NF-κB 的激活。此外,还通过 LPS 诱导的内毒素休克模型在小鼠中评估了 MTO 的保护作用。

结果

我们发现,MTO 可显著抑制 LPS 刺激的 NO 和 IL-6 的产生,而不影响细胞活力。MTO 抑制 LPS 诱导的 iNOS 和 COX-2 蛋白及其 mRNA 的表达。此外,MTO 还降低了 PMA 和离子霉素刺激的脾细胞中 TNF-α 和 IL-6 的分泌。因此,MTO 通过抑制 LPS 诱导的 p38 MAPK 和 NF-κB 激活来抑制 TNF-α 和 IL-6 等促炎细胞因子的产生。此外,MTO 通过抑制 TNF-α 的产生提高了致命性内毒素血症模型中小鼠的存活率,我们的 LC-MS 分析表明,MTO 的主要成分是枞酸内酯。

结论

我们在这里证明了东方杉二氯甲烷部分(MTO)在体外和体内可能抑制与炎症相关的生物标志物的证据,并且可能作为治疗炎症性疾病的潜在候选药物。

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