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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Anti-inflammatory effect and potential mechanism of betulinic acid on lambda-carrageenan-induced paw edema in mice
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Anti-inflammatory effect and potential mechanism of betulinic acid on lambda-carrageenan-induced paw edema in mice

机译:在小鼠中λ-carrageenan诱导的小鼠诱导诱导蛋白酸的抗炎作用及潜在机制

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lambda-Carrageenan (Carr), a seaweed polysaccharide, is used as a proinflammatory agent in research. Betulinic acid (BA), a naturally occurring pentacyclic triterpenoid, exerts immunomodulatory, antioxidant, anti-inflammatory, anti-tumor, anti-malarial and anti-HIV effects. The aim of this study was to investigate whether BA exerts anti-inflammatory effect against Carr-induced paw edema in mice, and how BA could mediate the expression of inflammation-associated MAPK-COX-2-PGE(2) signal pathway. BA pretreatment significantly reduced the in-flammatory response to Carr-induced paw edema, especially at 4 h after injection. BA reduced the serum levels of pro-inflammatory cytokines, such as IL-1 alpha, IL-1 beta, IL-5, IL-6, GM-CSF, KC, MCP-1 and PGE(2) in Carr-treated mice, and increased those of anti-inflammatory cytokines, such as IL-12. It also increased SOD, CAT and GSH-Px activities, and GSH content, and reduced MDA content in the liver of Carr-treated mice. Besides, BA reduced neutrophil infiltration in the basal and subcutaneous layers of the paw of Carr-treated mice, decreased the expression of COX-2 protein, and reduced the phosphorylation of JNK, p38 and ERK1/2. These results indicated that the protective effect of BA on Carr-induced paw edema might be due to its alleviation of inflammatory response and inhibition of oxidative stress, possibly by inhibiting MAPK-COX-2-PGE(2) signaling pathway activation.
机译:Lambda-carrageenan(Carr)是一种海藻多糖,用作研究中的促炎剂。桦木酸(BA),天然存在的五环三萜,施加免疫调节,抗氧化剂,抗炎,抗肿瘤,抗疟疾和抗HIV效应。本研究的目的是探讨BA是否对小鼠的CAR诱导的爪子水肿产生抗炎作用,以及BA如何介导炎症相关的MAPK-COX-2-PGE(2)信号途径的表达。 BA预处理显着降低了Carr诱导的爪水肿的易燃反应,特别是注射后4小时。 BA减少了核处理的小鼠中的促炎细胞因子的血清炎性细胞因子的血清炎症细胞因子,例如IL-1α,IL-1β,IL-5,IL-6,GM-CSF,KC,MCP-1和PGE(2) ,增加了抗炎细胞因子,例如IL-12。它还增加了SOD,CAT和GSH-PX活性,GSH含量,并降低了CAR治疗的小鼠肝脏中的MDA含量。此外,BA减少了CAR处理小鼠爪子的基底和皮下层中的中性粒细胞浸润,降低了COX-2蛋白的表达,并降低了JNK,P38和ERK1 / 2的磷酸化。这些结果表明,BA对Carr诱导的爪水肿的保护作用可能是由于其减轻了炎症反应和氧化应激的抑制,可能是通过抑制MAPK-COX-2-PGE(2)信号传导途径激活。

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