
IndraLab
Statements
reach
"proposed that significant cell death was observed only when P2X7R and NLRP3 inflammasome were both inhibited by ATP and MCC950, a specific inhibitor of NLRP3 inflammasome, and further research into safety manipulation of NLRP3 inflammasome without enhancing significant dose dependent side effects is required."
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"Both acute and chronic liver injury models were used: lipopolysaccharide (LPS)/adenosine-triphosphate (ATP) to induce in vivo NLRP3 activation, choline-deficient, L-amino acid-defined high-fat diet (CDAA-HFAT), and Western-type diet to induce fibrotic-non-alcoholic steatohepatitis (NASH)."
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"Importantly, we have previously demonstrated that MSC reduce the CVB3 induced ROS production in cardiomyocytes 18, whereas Oh et al. 20 recently illustrated that MSC decrease mitochondrial ROS and inhibit LPS- and ATP induced NLRP3 inflammasome activation in macrophages primarily by secreting STC-1."
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"Thus, our results indicated that methyl gallate was a classical NLRP3 inhibitor.Consistent with the results from mouse BMDMs, methyl gallate significantly reduced ATP-induced robust inflammasome activation in cultured PBMCs isolated from healthy subjects and inhibit the pre-activated NLRP3 inflammasome in patients’ SFCs."