Aiouea padiformis extract exhibits anti-inflammatory effects by inhibiting the ATPase activity of NLRP3

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作者
Sumin Lee
Qianying Ye
Hyeyun Yang
Sojung Lee
YeJi Kim
Nahyun Lee
Darwin Gonzalez-Cox
Dong-Keun Yi
Soo-Yong Kim
Sangho Choi
Taesoo Choi
Man S. Kim
Seong Su Hong
Chun Whan Choi
Yoonsung Lee
Yong Hwan Park
机构
[1] Ajou University School of Medicine,Department of Microbiology
[2] Kyung Hee University,Department of Biomedical Science and Technology
[3] Graduate School of Ajou University,Department of Biomedical Sciences
[4] Kyung Hee University,Clinical Research Institute, Kyung Hee University Hospital at Gangdong, School of Medicine
[5] Herbarium of National Autonomous University of Nicaragua at Leon,Department of Urology, School of Medicine
[6] International Biological Material Research Center,Natural Product Research Team
[7] Korea Research Institute of Bioscience and Biotechnology,undefined
[8] Kyung Hee University,undefined
[9] Gyeonggi Bio-Center,undefined
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关键词
NLRP3 inflammasome; Anti-inflammation; Plant extracts; Lauraceae;
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摘要
Inflammation is implicated as a cause in many diseases. Most of the anti-inflammatory agents in use are synthetic and there is an unmet need for natural substance-derived anti-inflammatory agents with minimal side effects. Aiouea padiformis belongs to the Lauraceae family and is primarily found in tropical regions. While some members of the Aiouea genus are known to possess anti-inflammatory properties, the anti-inflammatory properties of Aiouea padiformis extract (AP) have not been investigated. In this study, we aimed to examine the anti-inflammatory function of AP through the NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) inflammasome and elucidate the underlying mechanisms. Treatment with AP inhibited the secretion of interleukin-1 beta (IL-1β) mediated by NLRP3 inflammasome in J774A.1 and THP-1 cells without affecting the viability. In addition, AP treatment did not influence NF-κB signaling, potassium efflux, or intracellular reactive oxygen species (ROS) production—all of which are associated with NLRP3 inflammasome activation. However, intriguingly, AP treatment significantly reduced the ATPase activity of NLRP3, leading to the inhibition of ASC oligomerization and speck formation. Consistent with cellular experiments, the anti-inflammatory property of AP in vivo was also evaluated using an LPS-induced inflammation model in zebrafish, demonstrating that AP hinders NLRP3 inflammasome activation.
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