Xanthones are natural secondary metabolites that possess great potential as neuroprotective agents due to their prominent biological effects on Alzheimer's disease (AD). However, their underlying mechanisms in AD remain unclear. This study aimed to systematically review the effects and mechanisms of xanthones in cell culture and animal studies, gaining a better understanding of their roles in AD. A comprehensive literature search was conducted in the Medline and Scopus databases using specific keywords to identify relevant articles published up to June 2023. After removing duplicates, all articles were imported into the Rayyan software. The article titles were screened based on predefined inclusion and exclusion criteria. Relevant full-text articles were assessed for biases using the OHAT tool. The results were presented in tables. Xanthones have shown various pharmacological effects towards AD from the 21 preclinical studies included. Cell culture studies demonstrated the anti-cholinesterase activity of xanthones, which protects against the loss of acetylcholine. Xanthones exhibited neuroprotective effects by promoting cell viability, reducing the accumulation of β-amyloid and tau aggregation. The administration of xanthones in animal models resulted in a reduction in neuronal inflammation by decreasing microglial and astrocyte burden. In terms of molecular mechanisms, xanthones prevented neuroinflammation through the modulation of signaling pathways, including TLR4/TAK1/NF-κB and MAPK pathways. Mechanisms such as activation of caspase-3 and -9 and suppression of endoplasmic reticulum stress were also reported. Despite the various neuroprotective effects associated with xanthones, there are limited studies reported on their underlying mechanisms in AD. Further studies are warranted to fully understand their potential roles in AD.
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http://dx.doi.org/10.1007/s11064-023-04005-8 | DOI Listing |
Nat Prod Res
December 2024
College of Chemistry and Chemical Engineering, Xinjiang Agricultural University, Urumqi, China.
Seventeen compounds were isolated from the aerial parts of L., including 1 previously undescribed xanthone and 6 firstly isolated compounds. The structures of compounds were identified by Mass spectrometry and NMR spectroscopy.
View Article and Find Full Text PDFChem Biodivers
December 2024
Xiamen University, School of Pharmaceutical Sciences, South Xiangan Road, Xiamen, Fujian 361102, China, Xiamen, CHINA.
One undescribed xanthone, hypersine H(1), together with three known analogues, 3,7-dihydroxy-1-methoxyxanthone (2), 1,7-dihydroxy-5,6-dimethoxyxanthone (3), 1,5-dihydroxy-6,7-dimethoxyxanthone (4), were isolated from the whole plant of Hypericum elodeoides Choisy. Their structures including absolute configurations were unambiguously elucidated by HR-ESI-MS, extensive NMR spectroscopy and quantum chemical calculation of ECD method. Moreover, the anti-neuroinflammation activities of isolated compounds were evaluated.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, Pennsylvania19104, United States.
Cyclopentachromone, distinguished by its 6/6/5 heterotricyclic ring structure, is a key building block in many bioactive natural products, yet its enzymatic origin remains unclear. We identified a new class of cyclopentachromone-containing compounds, termed isochromosulfines, characterized by unique C-S bonds. A distinct FAD-dependent monooxygenase, IscL, was identified to catalyze the formation of the 6/6/5 cyclopentadiene intermediate, 2-remisporine A, from a 6/6/6 xanthone precursor via benzene ring contraction.
View Article and Find Full Text PDFFree Radic Res
December 2024
Graduate University of Science and Technology, VAST, Hanoi, Vietnam.
In this study, a quantum chemical exploration was conducted to assess the antioxidant activity of xanthones isolated from marine sources, focusing on thermodynamics and kinetics within simulated physiological environments. DFT analysis revealed that xanthones such as 1,4,7-trihydroxy-6-methylxanthone (), 1,4,5-trihydroxy-2-methylxanthone (), arthone C (), 2,3,4,6,8-pentahydroxy-1-methylxanthone (), sterigmatocystin (), oxisterigmatocystin C (), and oxisterigmatocystin D () favor the SPLET pathway in water and the FHT pathway in lipid environments. The kinetic study of these xanthones reacting with the hydroperoxyl radical (HOO•) was conducted using the formal hydrogen atom transfer (FHT) mechanism and the single electron transfer (SET) mechanism.
View Article and Find Full Text PDFMetabolomics
December 2024
LP2 Laboratory, Institute of Chemistry, Federal University of Mato Grosso Do Sul, Campo Grande, Brazil.
Introduction: The knowledge of the mode of action of an antimicrobial is essential for drug development and helps to fight against bacterial resistance. Thus, it is crucial to use analytical techniques to study the mechanism of action of substances that have potential to act as antibacterial agents OBJECTIVE: To use NMR-based metabolomics combined with chemometrics and molecular docking to identify the metabolic responses of Staphylococcus aureus following exposure to commercial antibiotics and some synthesized ω-aminoalkoxylxanthones.
Methods: Intracellular metabolites of S.
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