BACKGROUND:To date, Albatrellus fungi have been reported to produce over 80 natural products, including meroterpenoids, sesquiterpenes, and N-oxidized l-isoleucine derivatives with a wide range of bioactivities. Previous studies indicate that grifolin derivatives, a class of sesquiterpenes, have antioxidant capacity. However, the identification of these grifolin derivatives and their hepatoprotective activity, along with the underlying mechanisms, are yet to be explored.
PURPOSE:To identify the active hepatoprotective grifolin derivatives isolated from A. dispansus and to elucidate the mechanism of action both in vitro and in vivo.
METHODS:Grifolin derivatives from A. dispansus were isolated and elucidated according to comprehensive spectroscopic analyses, ECD spectra calculation, and Semisynthetic. The hepatoprotective potential of all compounds was initially screened by measuring cytotoxicity, apoptosis, and lactate dehydrogenase (LDH) release in CCl₄‑induced AML-12 cells. The most active compound was subsequently evaluated in a CCl₄‑induced liver injury mouse model. The underlying mechanism was further explored by RNA sequencing, RT‑qPCR, Western blotting, and immunofluorescence staining experiment to understand the intervention pathway.
RESULTS:Two grifolin derivatives, grifolin-4-l-ergothioneine (1) and grifolin-4,6-l-diergothioneine (2), were obtained from the ethanol extract of A. dispansus, together with two known compounds, l-(+)-ergothioneine (3) and grifolin (4). Compounds 1-3 displayed significant inhibition of CCl4-induced hepatocyte injury in vitro. In particular, 1 demonstrated potent protective effects against CCl4-induced liver damage in mice when administered at a dose of 15 mg/kg. A mechanistic study revealed that the liver protective effect of 1 was related to its role in the classic SIRT1/AMPK/NRF2 pathway.
CONCLUSION:This study provides the first comprehensive evidence of the hepatoprotective effects and underlying mechanisms of grifolin derivatives isolated from A. dispansus through integrated in vitro and in vivo investigations.
