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米奎尔提取物对脂多糖刺激的小鼠巨噬细胞RAW 264.7细胞的抗炎作用。

Anti-inflammatory effects of Miquel extracts in LPS-stimulated murine macrophage RAW 264.7 cells.

作者信息

Kim Jae-Hyun, Kim Minsun, Hong Sooyeon, Kwon Boguen, Song Min Wook, Song Kwangchan, Kim Eun-Young, Jung Hyuk-Sang, Sohn Youngjoo

机构信息

Department of Anatomy, College of Korean Medicine, Kyung Hee University, Seoul 02447, Republic of Korea.

出版信息

Exp Ther Med. 2021 May;21(5):429. doi: 10.3892/etm.2021.9846. Epub 2021 Feb 26.

Abstract

The aim of the present study was to demonstrate that Miquel extract exerts anti-inflammatory and antioxidant effects on lipopolysaccharide-stimulated RAW 264.7 cells. To confirm the inhibitory effect of ethyl acetate fraction of FTM (EAFM) on inflammation, the expression of nitric oxide (NO) and inflammatory cytokines was assessed by performing ELISA. Expression of intracellular mRNA and protein was confirmed by reverse transcription PCR and western blotting. In addition, the anti-inflammatory and anti-oxidant mechanisms of NF-κB, MAPK and heme oxygenase-1 (HO-1) were also investigated. EAFM significantly inhibited the expression of inflammatory factors including NO, IL-6 and TNF-α at non-toxic concentrations. EAFM also inhibited the mRNA and protein expression of inducible nitric oxide synthase in a concentration-dependent manner, but did not alter the expression of cyclooxygenase-2. Pre-treatment with EAFM inhibited the nuclear translocation of NF-κB, and suppressed the phosphorylation of ERK and JNK. In addition, EAFM induced 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) radical scavenging activity and an increase in the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) and HO-1. The results indicated that EAFM inhibited the expression of pro-inflammatory cytokines by inhibiting ERK/JNK phosphorylation and NF-κB translocation. EAFM also exerted antioxidant effects via Nrf2/HO-1 stimulation. Collectively, the results of the present study indicated that EAFM may be a valuable alternative for the treatment of a variety of inflammatory diseases.

摘要

本研究的目的是证明米奎尔提取物对脂多糖刺激的RAW 264.7细胞具有抗炎和抗氧化作用。为了证实FTM乙酸乙酯馏分(EAFM)对炎症的抑制作用,通过酶联免疫吸附测定法评估一氧化氮(NO)和炎性细胞因子的表达。通过逆转录PCR和蛋白质印迹法确认细胞内mRNA和蛋白质的表达。此外,还研究了核因子κB(NF-κB)、丝裂原活化蛋白激酶(MAPK)和血红素加氧酶-1(HO-1)的抗炎和抗氧化机制。EAFM在无毒浓度下显著抑制包括NO、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)在内的炎性因子的表达。EAFM还以浓度依赖性方式抑制诱导型一氧化氮合酶的mRNA和蛋白质表达,但不改变环氧合酶-2的表达。用EAFM预处理可抑制NF-κB的核转位,并抑制细胞外信号调节激酶(ERK)和应激活化蛋白激酶(JNK)的磷酸化。此外,EAFM诱导2,2'-联氮-双-(3-乙基苯并噻唑啉-6-磺酸)自由基清除活性,并增加核因子红细胞2相关因子2(Nrf2)和HO-1的表达。结果表明,EAFM通过抑制ERK/JNK磷酸化和NF-κB转位来抑制促炎细胞因子的表达。EAFM还通过刺激Nrf2/HO-1发挥抗氧化作用。总的来说,本研究结果表明,EAFM可能是治疗多种炎性疾病的一种有价值的替代物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34b9/7967825/832eaf2ffc53/etm-21-05-09846-g00.jpg

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