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Ultrafast ROS Scavenging Activity of Amur Maple Tree Extracts Confers Robust Cardioprotection for Myocardial Ischemia/Reperfusion Injury

  • Aoyang Pu (Co-first Author)
  • , Woo-Sup Sim (Co-first Author)
  • , Yuen-Kei Liem
  • , Yimin Lai
  • , Bong-Woo Park
  • , Kyoung-Tae Lee
  • , Hun-Jun Park*
  • , Kiwon Ban*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

9 Downloads (CityUHK Scholars)

Abstract

Ginnalin A (GA), a polyphenolic compound derived from amur maple trees, has been identified as a powerful scavenger of reactive oxygen species (ROS). Recognizing the pivotal role of ROS in exacerbating secondary damage during myocardial ischemia-reperfusion injury (MIRI), we fractionated GA-enriched extracts from the leaves of the amur maple tree, Acer tataricum L. subsp. ginnala (Maxim.) Wesm., using common solvents of dichloromethane (DCM) and ethyl acetate (EA). When co-administered for 30 min, the DCM- and EA-fractioned extracts effectively protected cardiomyocytes from H2O2-induced damage. ROS-sensitive probes indicated that treatment with ginnala extracts significantly reduced both intracellular and mitochondrial ROS levels. Instead of enhancing the activity of antioxidative enzymes, the ginnala extracts acted as natural antioxidases, directly scavenging various ROS such as superoxide, H2O2, hydroxyl radical, and Fe2+ within just 20 min. In a MIRI rat model, the in vivo administration of ginnala extracts provided significant cardioprotection by preserving viable myocardia and enhancing cardiac functions. Additionally, treatment with ginnala extracts significantly reduced cardiac fibrosis and denatured collagen. Our study suggests that the ultrafast ROS scavenging capability of ginnala extracts offers substantial heart protection during MIRI. Incorporating ginnala extracts as a pharmacological intervention during reperfusion could effectively mitigate ROS-induced cardiac injury.

© 2025 by the authors
Original languageEnglish
Article number671
Number of pages26
JournalAntioxidants
Volume14
Issue number6
DOIs
Publication statusPublished - 31 May 2025

Funding

This work was supported by the following funding: Tung Biomedical Sciences Centre, City University of Hong Kong (9609305 to K.B.), Futian Research Project (9609319 to K.B.), CityU ConRes_RMG (9239089 to K.B.), National Research Foundation of Korea grants (RS-2023-00219981 to K.B., RS-2024-00440285 to H.-J.P.) funded by the Korean government (MSIT).

Research Keywords

  • ischemia-reperfusion injury
  • anti-ROS
  • anti-ferroptosis
  • cardioprotection

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

RGC Funding Information

  • RGC-funded

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