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Premna odorata extract exhibits anti-inflammatory activity via suppression of NLRP3 inflammasome

  • Jaehyeok Lee,
  • Seyoung Kim,
  • Seongjong Lee,
  • Hangyeol Lee,
  • Hyeyun Yang,
  • Seoyeon Jang,
  • Sojin Yun,
  • Ja Hyang Cho,
  • Man S. Kim,
  • Hyung Won Ryu,
  • Jung Hee Kim,
  • Dong-Keun Yi,
  • Soo-Yong Kim,
  • SangHo Choi,
  • Sang Woo Lee,
  • Md. Salah Uddin,
  • Hyoung-Geun Kim,
  • Yoonsung Lee,
  • Yong Hwan Park

摘要

Premna odorata (family Verbenaceae), known as “Alagaw” in the Philippines, has traditionally been used to treat inflammatory respiratory conditions; however, molecular evidence supporting its pharmacological effects remains limited. Given that NOD-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome-driven IL-1β secretion plays a central role in inflammatory respiratory conditions, we investigated whether P. odorata extract (POE) modulates NLRP3 inflammasome activation. In LPS-primed J774A.1 and THP-1 macrophages, POE reduced IL-1β secretion induced by ATP or nigericin without affecting NLRC4 or AIM2 inflammasome activation, indicating NLRP3 selectivity. POE treatment inhibited adaptor apoptosis-associated speck-like protein containing CARD (ASC) oligomerization and speck formation without affecting cell viability or intracellular ROS levels, indicating suppression of inflammasome assembly. In vivo, POE attenuated inflammatory cell infiltration in an LPS-induced zebrafish model. Together, these findings indicate that POE suppresses NLRP3 inflammasome–mediated inflammatory responses, providing a molecular basis for its traditional use in managing inflammatory conditions and offering a promising natural scaffold for the development of NLRP3-targeted therapeutics.