Anti-Neuroinflammatory Effects of Compounds Isolated from Quercus acuta Thunb. Fruits via NF-κB Signaling Inhibition
Hwan Lee1, Yezhi Jin2, Ji-Ae Hong1
1Natural Resources Laboratory, Green Bio Headquarters, Jeonnam Bio Foundation (JBF), Jangheung-gun 59338, Jeollanam-do, Republic of Korea.
Abstract:
Aging is a major risk factor for neurodegenerative diseases in which microglia-driven neuroinflammation plays a critical role in neuronal dysfunction and disease progression. In this study, we sought to isolate bioactive metabolites from Quercus acuta Thunb. fruits-which have traditionally been used in oriental medicine but are chemically and pharmacologically underexplored-and evaluate their anti-neuroinflammatory potential. A total of 14 compounds were isolated from an ethanol extract of Q. acuta fruits through bioactivity-guided isolation, and their structures were identified by NMR spectroscopy. Notably, this study is the first to demonstrate that 3,5,7,2',6'-pentahydroxyflavanone and 2,5-dihydroxybenzaldehyde, among the compounds isolated from Q. acuta fruits, exhibit significant anti-neuroinflammatory activities. Both compounds reduced the production of proinflammatory mediators, including IL-6 and TNF-α, while inhibiting the expression of iNOS and COX-2. Moreover, they significantly inhibited NF-κB activation in lipopolysaccharide-induced BV2 microglia. Collectively, these findings indicate that Q. acuta fruits contain bioactive constituents with previously unreported anti-neuroinflammatory properties, supporting their potential as a natural source for the development of therapeutic agents targeting age-related neuroinflammation.
Related Concept Videos
NF-κB-dependent Signaling Pathway
NF-κB-dependent Signaling Mechanism
The...
Gene Regulation in Microbial Communities: Quorum Sensing
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...


