Silybin inhibits NLRP3 inflammasome assembly through the NAD+/SIRT2 pathway in mice with nonalcoholic fatty liver disease. Issue 2 (4th January 2018) - Zhang, Bangling
Abstract : Silybin is one of the effective, traditional Chinese medicines used as a hepatoprotective agent in nonalcoholic fatty liver disease (NAFLD) therapy worldwide, and the NOD‐like receptor family pyrin domain‐containing 3 (NLRP3) inflammasome has been recognized as an important factor involved in NAFLD development. However, little is known about the mechanisms of silybin in the regulation of high‐fat diet (HFD)–induced liver inflammation. In our study, we found that silybin inhibited endoplasmic reticulum stress and NLRP3 inflammasome activation in the livers of HFD‐fed mice and in cultured hepatocytes. Phosphorylation of inositol‐requiring enzyme (IRE) 1α and eIF2α, expression of thioredoxin‐interacting protein and cleaved caspase‐1, and release of IL‐1β were reduced by silybin. In addition, silybin inhibited the approach of calreticulin and translocase of outer membrane 20 (Tom20), prevented assembly of the NLRP3 inflammasome complex, and suppressed the accumulation of acetylated a‐tubulin in the perinuclear region. Both MEC‐17 and sirtuin 2 (SIRT2) were influenced by palmitate and silybin, whereas histone deacetylase 6 was not affected. In addition, supplementing NAD + directly or increasing NAD + concentration with silybin could maintain the activity of SIRT2. The anti‐inflammatory effect of silybin was blocked by SIRT2 silencing or by the SIRT2 inhibitor AGK2, as evidenced by NLRP3/ASC colocalization, AC‐α‐tubulin expression, and IL‐1β release. These findings indicate that the NAD + /SIRT2 pathway is an important mediator through which silybin prevents NLRP3 inflammasome activation during NAFLD.—Zhang, B., Xu, D., She, L., Wang, Z., Yang, N., Sun, R., Zhang, Y., Yan, C., Wei, Q., Aa, J., Liu, B., Wang G., Xie, Y. Silybin inhibits NLRP3 inflammasome assembly through the NAD+/SIRT2 pathway in mice with nonalcoholic fatty liver disease. FASEB J. 32, 757‐767 (2018). www.fasebj.org