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在小鼠结肠内给予Toll样受体7(TLR7)激动剂R-848会诱发急性局部和全身炎症。

Intra-colonic administration of the TLR7 agonist R-848 induces an acute local and systemic inflammation in mice.

作者信息

Karlsson Agneta, Jägervall Ke, Utkovic Helena, Karlsson Lisa, Rehnström Erika, Fredin Maria Fritsch, Gillberg Per-Göran, Jansson Liselotte, Michaëlsson Erik, Melgar Silvia

机构信息

Department of Integrative Pharmacology, AstraZeneca R&D Mölndal, Sweden.

出版信息

Biochem Biophys Res Commun. 2008 Mar 7;367(2):242-8. doi: 10.1016/j.bbrc.2007.12.046. Epub 2007 Dec 18.

Abstract

Imidazoquinoline compounds, such as resiquimod (R-848), are well known topically active immune modifiers that bind to toll-like receptor 7 (TLR7). The aim of this study was to characterize the R-848 induced inflammatory response in mice and to validate the response using methyl-prednisolone and anti-TNF antibody. Intra-colonic application of R-848 to BALB/c mice induced a systemic transient elevation of TNF, CXCL1, IL-6, and IL-12p40 and a colonic elevation of cytokines/chemokines and iNOS, without infiltration of immune cells or epithelial destruction. Treatment with methyl-prednisolone or anti-TNF antibody attenuated the systemic (TNF, IL-6, IL-12p40, and CXCL1) and local (colonic TNF and iNOS mRNA expression) response induced by R-848. In summary, intra-colonic administration of R-848 induces an acute systemic and local inflammatory response, which can be attenuated by steroids or anti-TNF antibody. We suggest that the R-848 inflammatory model can be useful in future validation of new drugs for gastrointestinal inflammatory conditions.

摘要

咪唑喹啉化合物,如咪喹莫特(R - 848),是众所周知的与Toll样受体7(TLR7)结合的局部活性免疫调节剂。本研究的目的是表征R - 848在小鼠中诱导的炎症反应,并使用甲基强的松龙和抗TNF抗体验证该反应。向BALB/c小鼠结肠内施用R - 848会导致TNF、CXCL1、IL - 6和IL - 12p40的全身性短暂升高,以及细胞因子/趋化因子和诱导型一氧化氮合酶(iNOS)在结肠中的升高,而没有免疫细胞浸润或上皮破坏。用甲基强的松龙或抗TNF抗体治疗可减弱R - 848诱导的全身性(TNF、IL - 6、IL - 12p40和CXCL1)和局部性(结肠TNF和iNOS mRNA表达)反应。总之,结肠内施用R - 848会诱导急性全身性和局部性炎症反应,类固醇或抗TNF抗体可减弱该反应。我们认为,R - 848炎症模型可能有助于未来验证用于胃肠道炎症性疾病的新药。

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