Xu Bao-Li, Wang Yuan-Yuan, Jiang Ling-Ling, Liu Zhen, Liu Ding-Rui, Zhao He, Li Shi-Liang, Wang Xiao-Bo
967th Hospital of People's Liberation Army, Dalian, China.
Department of Pharmacy, Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Front Pharmacol. 2023 Jan 9;13:1096137. doi: 10.3389/fphar.2022.1096137. eCollection 2022.
PM is an important environmental problem threatening human health at present, which poses serious harm to human body after inhalation. is a traditional Chinese medicine which exhibits anti-inflammatory effect. This study aimed to investigate the inhibitory effect of main phenolic acid components of on inflammation caused by PM. Effect of PM on cell activity and apoptosis were determined by MTT, flow cytometry and calcein AM/PI staining. PHBA, PHPAA, and mixture of PHBA and PHPAA of different concentrations were given to RAW264.7 cells pretreated with PM. The effect of drugs on cellular inflammatory factors was detected by ELISA. The expressions of TLRs related signal pathway at protein and gene levels were detected by western blot and qRT-PCR. The results showed that PM had no effect on cell activity and apoptosis within the determined concentration range. PHBA and PHPAA could markly inhibit the level of IL-1β, IL-6, and TNF-α in RAW264.7 cells. Furthermore, the expressions of TLR2, TLR4, MyD88, IRAK1, TRAF6, TAK1, IKKβ, and NF-κB induced by PM were markedly inhibited by PHBA and PHPAA at protein and gene levels. This study demonstrated that PHBA and PHPAA could attenuated inflammation caused by PM through suppressing TLRs related signal pathway.
颗粒物(PM)是当前威胁人类健康的一个重要环境问题,吸入后会对人体造成严重危害。[某种中药名称]是一种具有抗炎作用的中药。本研究旨在探讨[该中药名称]主要酚酸成分对PM所致炎症的抑制作用。通过MTT法、流式细胞术和钙黄绿素AM/PI染色检测PM对细胞活性和凋亡的影响。将不同浓度的对羟基苯甲酸(PHBA)、对羟基苯乙酸(PHPAA)以及PHBA与PHPAA的混合物给予经PM预处理的RAW264.7细胞。通过酶联免疫吸附测定(ELISA)检测药物对细胞炎症因子的影响。通过蛋白质印迹法(western blot)和实时定量聚合酶链反应(qRT-PCR)检测Toll样受体(TLRs)相关信号通路在蛋白质和基因水平的表达。结果表明,在测定的浓度范围内,PM对细胞活性和凋亡无影响。PHBA和PHPAA可显著抑制RAW264.7细胞中白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的水平。此外,PHBA和PHPAA在蛋白质和基因水平上显著抑制了由PM诱导的TLR2、TLR4、髓样分化因子88(MyD88)、白细胞介素-1受体相关激酶1(IRAK1)、肿瘤坏死因子受体相关因子6(TRAF6)、转化生长因子-β激活激酶1(TAK1)、核因子κB抑制蛋白激酶β(IKKβ)和核因子κB(NF-κB)的表达。本研究表明,PHBA和PHPAA可通过抑制TLRs相关信号通路减轻PM所致的炎症。