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is a perennial herb, and its stems are high-grade tea and nourishing medicinal materials. Various solvent extracts of were evaluated for their anti-inflammatory, anti-acetylcholinesterase (AChE), antioxidant, and anti-α-glucosidase properties. Acetone and EtOAc extracts showed significant antioxidant effects. Acetone, -hexane, and EtOAc extracts revealed potent inhibition against α-glucosidase. EtOAc, -hexane, and dichloromethane extracts displayed significant anti-AChE activity. Among the isolated constituents, gigantol, moscatin, and dendrophenol showed potent antioxidant activities in FRAP, DPPH, and ABTS radical scavenging tests. Moscatin (IC = 161.86 ± 16.45 μM) and dendrophenol (IC = 165.19 ± 13.25 μM) displayed more potent anti-AChE activity than chlorogenic acid (IC = 236.24 ± 15.85 μM, positive control). Dendrophenol (IC = 14.31 ± 3.17 μM) revealed more efficient anti-NO activity than quercetin (positive control, IC = 23.09 ± 1.43 μM). Analysis of AChE and iNOS inhibitory components was performed using molecular docking and/or the bioaffinity ultrafiltration method. In bioaffinity ultrafiltration, the binding affinity of compounds to the enzyme (acetylcholinesterase and inducible nitric oxide synthase) was determined using the enrichment factor (EF). Among the main components of the EtOAc extract from stem, moscatin, dendrophenol, gigantol, and batatasin III with acetylcholinesterase exhibited the highest binding affinities, with affinity values of 66.31%, 59.48%, 54.60%, and 31.87%, respectively. Moreover, the affinity capacity of the identified compounds with inducible nitric oxide synthase can be ranked as moscatin (88.99%) > dendrophenol (65.11%) > gigantol (44.84%) > batatasin III (27.18%). This research suggests that the bioactive extracts and components of stem could be studied further as hopeful candidates for the prevention or treatment of hyperglycemia, oxidative stress-related diseases, and nervous disorders.
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http://dx.doi.org/10.3390/antiox13080918 | DOI Listing |
Food Res Int
August 2025
Tea Research Institute Chinese Academy of Agricultural Sciences, National Engineering Research Center for Tea Processing, Key Laboratory of Tea Biology and Resources Utilization, Ministry of Agriculture, Hangzhou, China. Electronic address:
The search for natural α-glucosidase (α-Glu) inhibitors has gained significant attention in developing novel antidiabetic agents or functional foods. Low-temperature fermented Jinxuan black tea represents a promising source of such bioactive compounds. Sixteen potential α-Glu inhibitors were identified from the tea using 10 kDa affinity ultrafiltration.
View Article and Find Full Text PDFBiochem Biophys Res Commun
August 2025
Department of Pharmacy, The Second Hospital of Hebei Medical University, Shijiazhuang, PR China; State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, PR China. Electronic address:
Oroxylum indicum (O. indicum) is a common traditional Chinese medicine, but its neuroprotective effects in Parkinson's disease (PD) model have not been fully elaborated. Mitochondrial complex I dysfunction is the core pathology of oxidative stress injury in PD, and the mechanism of regulating the activity of its key subunit NADH: Ubiquinone Oxidoreductase Core Subunit S3 (NDUFS3) has not been clarified.
View Article and Find Full Text PDFJ Chromatogr B Analyt Technol Biomed Life Sci
July 2025
School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, Liaoning 110016, China. Electronic address:
Acetylcholinesterase (AChE) is widely concerned as a hotspot target for the treatment of Alzheimer's disease (AD). This study aimed to screen AChE inhibitors from walnut kernel (WK) through the techniques combined of bio-affinity ultrafiltration, AChE-functionalized magnetic nanoparticles and UPLC-Q-Exactive Orbitrap MS. The results showed that WK extract improved acetylcholine level and reduced AChE level in the hippocampus and cortex of AD mice with kidney yang deficiency.
View Article and Find Full Text PDFJ Ethnopharmacol
February 2025
Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, 221004, China; Department of Pharmacy, Suining People's Hospital Affiliated to Xuzhou Medical University, Suining, 221202, China; Department of Pharmaceutical Analysis, Xuzhou Medical University, Xu
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View Article and Find Full Text PDFNat Prod Res
November 2024
Key Laboratory of Phytochemistry, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji, China.
This study conducted a systematic analysis to explore natural DNA topoisomerase I (topo I) inhibitors from (). Crude extract of exhibited notable toxic and anti-proliferative effects on A549 cells. A total of 36 components were identified using bioaffinity ultrafiltration UPLC-ESI-MS/MS.
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