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姜黄素,一种膳食生物活性化合物,通过刺激结肠上皮 PPAR-γ 转录因子的表达发挥其在结肠炎中的抗炎作用。

Thymoquinone, a Dietary Bioactive Compound, Exerts Anti-Inflammatory Effects in Colitis by Stimulating Expression of the Colonic Epithelial PPAR-γ Transcription Factor.

机构信息

Department of Physiology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain PO Box 17666, United Arab Emirates.

Zayed Bin Sultan Center for Health Sciences, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain PO Box 17666, United Arab Emirates.

出版信息

Nutrients. 2021 Apr 17;13(4):1343. doi: 10.3390/nu13041343.

Abstract

Inflammatory bowel diseases (IBD) are chronic inflammatory disorders with increasing incidence and prevalence worldwide. Here, we investigated thymoquinone (TQ), a naturally occurring phytochemical present in , for anti-inflammatory effects in colonic inflammation. To address this, we used in vivo (mice) and in vitro (HT-29 cells) models in this investigation. Our results showed that TQ treatment significantly reduced the disease activity index (DAI), myeloperoxidase (MPO) activity, and protected colon microscopic architecture. In addition, TQ also reduced the expression of proinflammatory cytokines and mediators at both the mRNA and protein levels. Further, TQ decreased phosphorylation of the activated mitogen-activated protein kinase (MAPK) signaling pathway and nuclear factor kappa B (NF-κB) proteins and enhanced colon epithelial PPAR-γ transcription factor expression. TQ significantly decreased proinflammatory chemokines (CXCL-1 and IL-8), and mediator (COX-2) mRNA expression in HT-29 cells treated with TNF-α. TQ also increased HT-29 PPAR-γ mRNA, PPAR-γ protein expression, and PPAR-γ promoter activity. These results indicate that TQ inhibits MAPK and NF-κB signaling pathways and transcriptionally regulates PPAR-γ expression to induce potent anti-inflammatory activity in vivo and in vitro models of colon inflammation.

摘要

炎症性肠病(IBD)是一种慢性炎症性疾病,全球发病率和患病率不断增加。在这里,我们研究了存在于 的姜黄素(TQ)作为一种天然存在的植物化学物质,具有抗炎作用。为了解决这个问题,我们在这项研究中使用了体内(小鼠)和体外(HT-29 细胞)模型。我们的结果表明,TQ 治疗可显著降低疾病活动指数(DAI)、髓过氧化物酶(MPO)活性,并保护结肠微观结构。此外,TQ 还可降低促炎细胞因子和介质的 mRNA 和蛋白水平表达。此外,TQ 可减少激活的丝裂原活化蛋白激酶(MAPK)信号通路和核因子 kappa B(NF-κB)蛋白的磷酸化,并增强结肠上皮细胞 PPAR-γ 转录因子的表达。TQ 可显著降低 TNF-α处理的 HT-29 细胞中促炎趋化因子(CXCL-1 和 IL-8)和介质(COX-2)的 mRNA 表达。TQ 还增加了 HT-29 的 PPAR-γ mRNA、PPAR-γ 蛋白表达和 PPAR-γ 启动子活性。这些结果表明,TQ 可抑制 MAPK 和 NF-κB 信号通路,并通过转录调节 PPAR-γ 表达,从而在体内和体外结肠炎症模型中诱导有效的抗炎活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aec/8073634/9558f16dbb77/nutrients-13-01343-g001.jpg

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