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New autophagy-modulating lanostane-type triterpenoids from a hallucinogenic poisonous mushroom Gymnopilus orientispectabilis

  • Seulah Lee
  • , Mina Jang
  • , Rhim Ryoo
  • , Jongtae Roh
  • , Sung Kyun Ko
  • , Ki Hyun Kim
  • Sungkyunkwan University
  • Kyung Hee University
  • Korea Research Institute of Bioscience and Biotechnology
  • Daegu-Gyeongbuk Medical Innovation Foundation
  • National Institute of Forest Science
  • University of Science and Technology UST

Research output: Contribution to journalArticlepeer-review

Abstract

Gymnopilus orientispectabilis, also known as “big laughter mushroom,” is a hallucinogenic poisonous mushroom that causes excessive laughter upon ingestion. From the fruiting bodies of G. orientispectabilis, eight lanostane-type triterpenoids (1–8), including seven novel compounds: gymnojunols A-G (2–8), were isolated. The chemical structures of these new compounds (2–8) were determined by analyzing their 1D and 2D NMR spectra and HR-EISMS, and their absolute configurations were unambiguously assigned by quantum chemical ECD calculations and a computational method coupled with a statistical procedure (DP4+). Upon evaluating autophagic activity, compounds 2, 6, and 7 increased LC3B-II levels in HeLa cells to a similar extent as bafilomycin, an autophagy inhibitor. In contrast, compound 8 decreased the levels of both LC3B-I and LC3B-II, and a similar effect was observed following treatment with rapamycin, an autophagy inducer. Our findings provide experimental evidence for new potential autophagy modulators in the hallucinogenic poisonous mushroom G. orientispectabilis.

Original languageEnglish
Pages (from-to)272-287
Number of pages16
JournalArchives of Pharmacal Research
Volume47
Issue number3
DOIs
StatePublished - Mar 2024

Keywords

  • Autophagic activity
  • ECD calculation
  • Gymnopilus orientispectabilis
  • Lanostane-type triterpenoids
  • Structural elucidation

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