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Toll 样受体 4(TLR4)拮抗剂作为治疗肠道炎症的潜在疗法。

Toll-like receptor 4 (TLR4) antagonists as potential therapeutics for intestinal inflammation.

机构信息

Discipline of Physiology, Adelaide Medical School, University of Adelaide, Adelaide, South Australia, 5005, Australia.

Discipline of Pharmacology, Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia.

出版信息

Indian J Gastroenterol. 2021 Feb;40(1):5-21. doi: 10.1007/s12664-020-01114-y. Epub 2021 Mar 5.

Abstract

Gastrointestinal inflammation is a hallmark of highly prevalent disorders, including cancer treatment-induced mucositis and ulcerative colitis. These disorders cause debilitating symptoms, have a significant impact on quality of life, and are poorly managed. The activation of toll-like receptor 4 (TLR4) has been proposed to have a major influence on the inflammatory signalling pathways of the intestinal tract. Inhibition of TLR4 has been postulated as an effective way to treat intestinal inflammation. However, there are a limited number of studies looking into the potential of TLR4 antagonism as a therapeutic approach for intestinal inflammation. This review surveyed available literature and reported on the in vitro, ex vivo and in vivo effects of TLR4 antagonism on different models of intestinal inflammation. Of the studies reviewed, evidence suggests that there is indeed potential for TLR4 antagonists to treat inflammation, although only a limited number of studies have investigated treating intestinal inflammation with TLR4 antagonists directly. These results warrant further research into the effect of TLR4 antagonists in the intestinal tract.

摘要

胃肠道炎症是多种高发疾病的一个特征,包括癌症治疗引起的黏膜炎和溃疡性结肠炎。这些疾病会导致使人虚弱的症状,对生活质量有重大影响,且难以治疗。Toll 样受体 4(TLR4)的激活被认为对肠道的炎症信号通路有重大影响。抑制 TLR4 被认为是治疗肠道炎症的一种有效方法。然而,目前只有少数研究探讨 TLR4 拮抗作用作为治疗肠道炎症的一种治疗方法的潜力。本综述调查了现有文献,并报告了 TLR4 拮抗作用对不同肠道炎症模型的体外、离体和体内影响。在综述的研究中,有证据表明 TLR4 拮抗剂确实有治疗炎症的潜力,尽管只有少数研究直接用 TLR4 拮抗剂治疗肠道炎症。这些结果表明需要进一步研究 TLR4 拮抗剂在肠道中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f1/7934812/88d670934270/12664_2020_1114_Fig1_HTML.jpg

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