Selective Inhibition of Human Monoamine Oxidase B by 5-Hydroxy-2-methyl-chroman-4-one Isolated from an Endogenous Lichen Fungus <i>Daldinia fissa</i>

Inhibitory activities against monoamine oxidases (MAOs) and cholinesterases (ChEs) and antioxidant activity were evaluated for 195 extracts from Ukraine-derived endogenous lichen fungi (ELF). Among them, an ELF13 (identified as <i>Daldinia fissa</i>) extract showed the highest inhibitory...

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Bibliographic Details
Main Authors: Geum-Seok Jeong, Myung-Gyun Kang, Sang-Ah Han, Ji-In Noh, Jong-Eun Park, Sang-Jip Nam, Daeui Park, Sung-Tae Yee, Hoon Kim
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Journal of Fungi
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Online Access:https://www.mdpi.com/2309-608X/7/2/84
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Summary:Inhibitory activities against monoamine oxidases (MAOs) and cholinesterases (ChEs) and antioxidant activity were evaluated for 195 extracts from Ukraine-derived endogenous lichen fungi (ELF). Among them, an ELF13 (identified as <i>Daldinia fissa</i>) extract showed the highest inhibitory activity against MAO-B, and 5-hydroxy-2-methyl-chroman-4-one (HMC) was isolated as a ~ 4-fold selective inhibitor of MAO-B (IC<sub>50</sub> = 3.23 µM) compared to MAO-A (IC<sub>50</sub> = 13.97 µM). HMC is a reversible competitive inhibitor with a K<sub>i</sub> value of 0.896 µM. No cytotoxicity was observed in normal and cancer cells at 50 µM of HMC. HMC showed blood–brain barrier permeability and high gastrointestinal absorption in silico pharmacokinetics. The docking simulation results showed that the binding affinity of HMC for MAO-B (−7.3 kcal/mol) was higher than that of MAO-A (−6.1 kcal/mol) and that HMC formed a hydrogen bond interaction with Cys172 of MAO-B (distance: 3.656 Å), whereas no hydrogen bonding was predicted with MAO-A. These results suggest that HMC can be considered a candidate for the treatment of neurodegenerative diseases, such as Alzheimer’s disease and Parkinson’s disease.
ISSN:2309-608X