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预防性和治疗性 euphol 治疗可减轻小鼠实验性结肠炎。

Preventive and therapeutic euphol treatment attenuates experimental colitis in mice.

机构信息

Department of Pharmacology, Centre of Biological Sciences, Universidade Federal de Santa Catarina, Florianópolis, Brazil.

出版信息

PLoS One. 2011;6(11):e27122. doi: 10.1371/journal.pone.0027122. Epub 2011 Nov 2.

Abstract

BACKGROUND

The tetracyclic triterpene euphol is the main constituent found in the sap of Euphorbia tirucalli. This plant is widely known in Brazilian traditional medicine for its use in the treatment of several kinds of cancer, including leukaemia, prostate and breast cancers. Here, we investigated the effect of euphol on experimental models of colitis and the underlying mechanisms involved in its action.

METHODOLOGY/PRINCIPAL FINDINGS: Colitis was induced in mice either with dextran sulfate sodium (DSS) or with 2,4,6-trinitrobenzene sulfonic acid (TNBS), and the effect of euphol (3, 10 and 30 mg/kg) on colonic injury was assessed. Pro-inflammatory mediators and cytokines were measured by immunohistochemistry, enzyme-Linked immunoabsorbent assay (ELISA), real time-polymerase chain reaction (RT-PCR) and flow cytometry. Preventive and therapeutic oral administration of euphol attenuated both DSS- and TNBS-induced acute colitis as observed by a significant reduction of the disease activity index (DAI), histological/microscopic damage score and myeloperoxidase (MPO) activity in colonic tissue. Likewise, euphol treatment also inhibited colon tissue levels and expression of IL-1β, CXCL1/KC, MCP-1, MIP-2, TNF-α and IL-6, while reducing NOS2, VEGF and Ki67 expression in colonic tissue. This action seems to be likely associated with inhibition of activation of nuclear factor-κB (NF-κB). In addition, euphol decreased LPS-induced MCP-1, TNF-α, IL-6 and IFN-γ, but increased IL-10 secretion from bone marrow-derived macrophages in vitro. Of note, euphol, at the same schedule of treatment, markedly inhibited both selectin (P- and E-selectin) and integrin (ICAM-1, VCAM-1 and LFA-1) expression in colonic tissue.

CONCLUSIONS/SIGNIFICANCE: Together, these results clearly demonstrated that orally-administered euphol, both preventive or therapeutic treatment were effective in reducing the severity of colitis in two models of chemically-induced mouse colitis and suggest this plant-derived compound might be a potential molecule in the management of inflammatory bowel diseases.

摘要

背景

五环三萜化合物表柯里拉京是大戟(Euphorbia tirucalli)树液中的主要成分。这种植物在巴西传统医学中被广泛用于治疗多种癌症,包括白血病、前列腺癌和乳腺癌。在这里,我们研究了表柯里拉京对结肠炎实验模型的影响及其作用的潜在机制。

方法/主要发现:用葡聚糖硫酸钠(DSS)或 2,4,6-三硝基苯磺酸(TNBS)诱导小鼠结肠炎,并评估表柯里拉京(3、10 和 30 mg/kg)对结肠损伤的影响。通过免疫组织化学、酶联免疫吸附试验(ELISA)、实时聚合酶链反应(RT-PCR)和流式细胞术测量促炎介质和细胞因子。预防性和治疗性口服表柯里拉京可减轻 DSS 和 TNBS 诱导的急性结肠炎,表现为疾病活动指数(DAI)、组织学/显微镜损伤评分和结肠组织髓过氧化物酶(MPO)活性显著降低。同样,表柯里拉京治疗还抑制了结肠组织中 IL-1β、CXCL1/KC、MCP-1、MIP-2、TNF-α和 IL-6 的水平和表达,同时降低了结肠组织中 NOS2、VEGF 和 Ki67 的表达。这种作用可能与抑制核因子-κB (NF-κB)的激活有关。此外,表柯里拉京还降低了 LPS 诱导的 MCP-1、TNF-α、IL-6 和 IFN-γ的表达,但增加了骨髓来源的巨噬细胞中 IL-10 的分泌。值得注意的是,表柯里拉京在相同的治疗方案下,显著抑制了结肠组织中选择素(P-和 E-选择素)和整合素(ICAM-1、VCAM-1 和 LFA-1)的表达。

结论/意义:综上所述,这些结果清楚地表明,口服表柯里拉京,无论是预防还是治疗,都能有效减轻两种化学诱导的小鼠结肠炎模型中结肠炎的严重程度,并表明这种植物衍生的化合物可能是治疗炎症性肠病的潜在分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c446/3206917/2638e536b9ba/pone.0027122.g001.jpg

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