Department of Cosmetic Science and Technology, Seowon University, Cheongju, 28674, Republic of Korea.
College of Pharmacy, CMRI, Research Institute of Pharmaceutical Sciences, BK21 Plus KNU Multi-Omics based Creative Drug Research Team, Kyungpook National University, 80 Dahak-ro, Buk-gu, Daegu, 41566, Republic of Korea.
J Nat Med. 2020 Jan;74(1):90-97. doi: 10.1007/s11418-019-01348-x. Epub 2019 Jul 26.
The aim of this study was to investigate the effects of two structurally related flavonoids found in Cyclopia subternata, vicenin-2 (VCN) and scolymoside (SCL) on lipopolysaccharide (LPS)-induced liver failure in mice and to elucidate underlying mechanisms. Mice were treated intravenously with VCN or SCL at 12 h after LPS treatment. LPS significantly increased mortality, serum levels of alanine transaminase, aspartate transaminase, and inflammatory cytokines, and toll-like receptor 4 (TLR4) protein expression; these effects of LPS were inhibited by VCN or SCL. It also attenuated the LPS-induced activation of myeloid differentiation primary response gene 88 and TLR-associated activator of interferon-dependent signaling pathways of the TLR system. Our results suggest that VCN or SCL protects against LPS-induced liver damage by inhibiting the TLR-mediated inflammatory pathway, indicating its potential to treat liver diseases.
本研究旨在探讨南非叶中两种结构相关的类黄酮(vicenin-2 和 scolymoside)对脂多糖(LPS)诱导的小鼠肝衰竭的影响,并阐明其潜在机制。小鼠在 LPS 处理后 12 小时经静脉注射给予 VCN 或 SCL。LPS 显著增加了死亡率、血清丙氨酸转氨酶、天冬氨酸转氨酶和炎症细胞因子水平,以及 Toll 样受体 4(TLR4)蛋白表达;这些 LPS 的作用被 VCN 或 SCL 抑制。它还减弱了 LPS 诱导的髓样分化初级反应基因 88 和 TLR 相关干扰素依赖性信号通路的激活。我们的结果表明,VCN 或 SCL 通过抑制 TLR 介导的炎症通路来保护 LPS 诱导的肝损伤,表明其在治疗肝脏疾病方面的潜力。