Therapeutic potential of the medicinal mushroom Ganoderma lucidum against Alzheimer's disease - 29/02/24
Abstract |
Alzheimer’s disease (AD) is a high-incidence neurodegenerative disorder, characterized by cognitive impairment, memory loss, and psychiatric abnormalities. Ganoderma lucidum is a famous medicinal fungus with a long history of dietary intake, containing various bioactive components, and have been documented to exhibit antioxidant, anti-inflammatory, anti-tumor, anti-aging, and immunomodulatory effects, among others. Recent studies have shown that G. lucidum and its components have promising therapeutic potential against AD from various aspects, which can delay the progression of AD, improve cognitive function and quality of life. The underlying mechanisms mainly include inhibiting tau hyperphosphorylation, inhibiting Aβ formation, affecting activated microglia, regulating NF-κB/MAPK signalling pathway, inhibiting neuronal apoptosis, modulating immune system, and inhibiting acetylcholinesterase, etc. This paper systematically reviewed the relevant studies on the therapeutic potential of G. lucidum and its active components for treatment of AD, key points related with the mechanism studies and clinical trials have been discussed, and further perspectives have been proposed. Totally, as a natural medicinal mushroom, G. lucidum has the potential to be developed as effective adjuvant for AD treatment owing to its therapeutic efficacy against multiple pathogenesis of AD. Further mechanical investigation and clinical trials can help unlock the complete potential of G. lucidum as a therapeutic option for AD.
Le texte complet de cet article est disponible en PDF.Graphical Abstract |
Highlights |
• | G. lucidum exhibits therapeutic potential against Alzheimer's disease. |
• | Polysaccharides and triterpenes represent main bioactive components of G. lucidum. |
• | G. lucidum has a good safety profile within reasonable dosage ranges. |
• | G. lucidum and its components can target multiple aspects of AD pathology. |
Abbreviations : AA, ACetylCoA, ACh, AChE, AD, ADAS-cog, APP, ATP, Aβ, BDNF, CaSR, CAT, CDK5, CGI, CNS, CoA, cPLA2, Cyt c, DAP12, DeGA F, DEVD, EGL, FDA, FIP-glu, G. lucidum, GA, GAA, GAB, GAD, GLAQ, GLBR, GLE, GLEA, GLP, GLS, GLTs, GSK3β, GT-2, hAMSCs, IL-1β, IL-6, IL-8, iNOS, JNK, LDH, LPS, mAChRs, MAPK, MDA, mGluR, mito-p53, MS, N/A-SMase, ND2/4, NFTs, NF-κB, NK, NLRP3, NMDA, NO, NPC, NPI, oAβ, p38-PKB, PP2A, pro-IL-1β, ROCK, ROS, SIRT3, SOD, SPGL, SYK, TCA, TNF-α, TREM2, WHOQOL-BREF, α7 nAChR
Keywords : Ganoderma lucidum, Neurodegenerative disorder, Alzheimer's disease, Active components, Mechanisms, Clinical trails
Plan
Vol 172
Article 116222- mars 2024 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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