| Literature DB >> 31032942 |
Yuanling Huang1, Ting Wan2, Nengzhi Pang1, Yujia Zhou1, Xuye Jiang1, Bangyan Li1, Yingying Gu1, Yufeng Huang3, Xiaodie Ye3, Hui Lian3, Zhenfeng Zhang3, Lili Yang1.
Abstract
Cannabidiol (CBD), an abundant nonpsychoactive constituent of marijuana, has been reported previously to protect against hepatic steatosis. In this study, we studied further the functions and mechanisms of CBD on liver inflammation induced by HFC diet. Mice feeding an HFC diet for 8 weeks were applied to test the protective effect of CBD on livers. RAW264.7 cells were incubated with LPS + ATP ± CBD to study the mechanisms of the effect of CBD against inflammasome activation. We found that CBD alleviated liver inflammation induced by HFC diet. CBD significantly inhibited the nuclear factor-κappa B (NF-κB) p65 nuclear translocation and the activation of nucleotide-binding domain like receptor protein 3 (NLRP3) inflammasome both in vivo and in vitro studies, which lead to the reduction of the expression of inflammation-related factors in our studies. In addition, Inhibitor of activation of NF-κB partly suppressed the NLRP3 inflammasome activation, while adding CBD further inhibited NF-κB activation and correspondingly suppressed the NLRP3 inflammasome activation in macrophages. In conclusion, the suppression of the activation of NLRP3 inflammasome through deactivation of NF-κB in macrophages by CBD might be one mechanism of its anti-inflammatory function in the liver.Entities:
Keywords: NF-κB; NLRP3 inflammasome; cannabidiol; nonalcoholic steatohepatitis
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Year: 2019 PMID: 31032942 DOI: 10.1002/jcp.28728
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384