Chu Hongqian, Tang Qiuqiong, Huang Hongpeng, Hao Weidong, Wei Xuetao
Department of Toxicology, School of Public Health, Peking University, Beijing Key Laboratory of Toxicological Research and Risk Assessment for Food Safety, Beijing 100191, PR China.
Department of Toxicology, School of Public Health, Peking University, Beijing Key Laboratory of Toxicological Research and Risk Assessment for Food Safety, Beijing 100191, PR China.
Environ Toxicol Pharmacol. 2016 Jan;41:159-66. doi: 10.1016/j.etap.2015.11.018. Epub 2015 Dec 7.
Grape-seed proanthocyanidins (GSPs) have been shown to function as an anti-oxidant and anti-inflammatory agent with little toxicity in vivo and in vitro. However, little is known about their anti-inflammatory properties and mechanisms of action. The specific focus being its effects on the MAP kinases and nuclear factor-kappaB (NF-κB) signal transduction pathways in lipopolysaccharide (LPS) -stimulated RAW264.7 cells. GSPs extract has been found to suppress the mRNA expression of pro-inflammatory cytokines like tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and inflammatory molecule of cyclooxygenase-2 (COX-2) while mRNA level of IL-10 was greatly promoted. Furthermore, GSPs extract inhibited the expression of phosphorylated ERK, JNK and P38, as well as phosphorylated IKKα/β and NF-κB p65 subunit. In conclusion, our results show that GSPs extract showed its anti-inflammatory and immunomodulatory properties by suppressing the activation of MAP kinases and NF-κB signal transduction pathways.
葡萄籽原花青素(GSPs)已被证明在体内和体外均具有抗氧化和抗炎作用,且毒性较小。然而,人们对其抗炎特性和作用机制知之甚少。具体研究重点是其对脂多糖(LPS)刺激的RAW264.7细胞中丝裂原活化蛋白激酶(MAP激酶)和核因子-κB(NF-κB)信号转导通路的影响。已发现GSPs提取物可抑制促炎细胞因子如肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)的mRNA表达以及环氧合酶-2(COX-2)的炎症分子表达,同时IL-10的mRNA水平显著升高。此外,GSPs提取物抑制磷酸化ERK、JNK和P38的表达,以及磷酸化IKKα/β和NF-κB p65亚基的表达。总之,我们的结果表明,GSPs提取物通过抑制MAP激酶和NF-κB信号转导通路的激活而表现出其抗炎和免疫调节特性。