幽门螺杆菌
炎症
山奈酚
炎症反应
微生物学
消炎药
免疫学
生物
化学
类黄酮
生物化学
抗氧化剂
遗传学
作者
Min Ji Yeon,Min Ho Lee,Do Hyun Kim,Ji Yeong Yang,Hyun Jun Woo,Hye Jin Kwon,Chéol Moon,Sa‐Hyun Kim,Jong‐Bae Kim
标识
DOI:10.1080/09168451.2018.1528140
摘要
ABSTRACT Inflammation induced by Helicobacter pylori infection related to gastric carcinogenesis. In this study, we have investigated the anti-inflammatory effect and its mechanism of kaempferol in the inflammatory response caused by H. pylori infection in vitro. We found that kaempferol reduced the expression of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-8) and production of IL-8 in AGS cells. In addition, kaempferol suppressed translocation of cytotoxin-associated gene A (CagA) and vacuolating cytotoxin A (VacA) of H. pylori to AGS cells. It was due to decreased transcription of type IV secretion system (T4SS) components involved in CagA injection and secretion system subunit protein A (SecA) of type V secretion system (T5SS) involved in VacA secretion by kaempferol. In conclusion, kaempferol shows the anti-inflammatory effect by suppressing the translocation of CagA and VacA proteins and leading to the down-regulation of pro-inflammatory cytokines. Abbreviations: CagA: cytotoxin-associated gene A; VacA: vacuolating cytotoxin A; T4SS: type IV secretion systems; SecA: secretion system subunit protein A; T5SS: type V secretion system;
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