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Reishi, Lingzhi · 2024 · Journal Article

High relevance

Rapid Discovery of Aβ42 Fibril Disintegrators from Ganoderma lucidum via Ligand Fishing and Their Neuroprotective Effects on Alzheimer's Disease.

Ganoderma lucidum

OncologyImmune supportCognition & nervesMetabolic health
SpeciesReishi, Lingzhi
JournalJournal of agricultural and food chemistry
Year2024

Key points

  • An amyloid-β (Aβ) fibril is a vital pathogenic factor of Alzheimer's disease (AD)
  • Here, a ligand fishing method was employed to rapidly discover Aβ 42 fibril disintegrators from Ganoderma lucidum using Aβ 42 fibril-immobilized magnetic beads, which led to the isolation of six Aβ 42 fibril disintegrators including ganodermanontriol, ganoderic acid DM, ganoderiol F, ganoderol B, ganodermenonol, and ergosterol
  • Neuroprotective evaluation in vitro exhibited that these Aβ 42 fibril disintegrators could significantly mitigate Aβ 42 -induced neurotoxicity
  • Among these six disintegrators, ergosterol and ganoderic acid DM with stronger protecting activity were further selected to evaluate their neuroprotective effect on AD in vivo
  • Results showed that ergosterol and ganoderic acid DM could significantly alleviate Aβ 42 -induced cognitive dysfunction and hippocampus neuron loss in vivo
  • Moreover, ergosterol and ganoderic acid DM could significantly inhibit Aβ 42 -induced neuron apoptosis and Nrf2-mediated neuron oxidative stress in vitro and in vivo

Metadata-grounded summary

Citation abstract

An amyloid-β (Aβ) fibril is a vital pathogenic factor of Alzheimer's disease (AD). Aβ fibril disintegrators possess great potential to be developed into novel anti-AD agents. Here, a ligand fishing method was employed to rapidly discover Aβ 42 fibril disintegrators from Ganoderma lucidum using Aβ 42 fibril-immobilized magnetic beads, which led to the isolation of six Aβ 42 fibril disintegrators including ganodermanontriol, ganoderic acid DM, ganoderiol F, ganoderol B, ganodermenonol, and ergosterol. Neuroprotective evaluation in vitro exhibited that these Aβ 42 fibril disintegrators could significantly mitigate Aβ 42 -induced neurotoxicity. Among these six disintegrators, ergosterol and ganoderic acid DM with stronger protecting activity were further selected to evaluate their neuroprotective effect on AD in vivo. Results showed that ergosterol and ganoderic acid DM could significantly alleviate Aβ 42 -induced cognitive dysfunction and hippocampus neuron loss in vivo. Moreover, ergosterol and ganoderic acid DM could significantly inhibit Aβ 42 -induced neuron apoptosis and Nrf2-mediated neuron oxidative stress in vitro and in vivo.

Citation

Li QM, Han HH, Zang DD, Zha XQ, Zhou A, Zhang FY, et al. (2024). Rapid Discovery of Aβ42 Fibril Disintegrators from Ganoderma lucidum via Ligand Fishing and Their Neuroprotective Effects on Alzheimer's Disease. Journal of agricultural and food chemistry https://doi.org/10.1021/acs.jafc.3c08664 PMID: 38362879

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