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 language | English |
|---|---|
| Pages (from-to) | 272-287 |
| Number of pages | 16 |
| Journal | Archives of Pharmacal Research |
| Volume | 47 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 2024 |
Keywords
- Autophagic activity
- ECD calculation
- Gymnopilus orientispectabilis
- Lanostane-type triterpenoids
- Structural elucidation
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