Optimization and Metabolomic Profiling of Wolffia globosa Extract Reveal Multitarget Neuroprotective Activity Against Alzheimer’s Disease with In Vitro, In Silico, and In Vivo Validation
| dc.contributor.author | Temviriyanukul P. | |
| dc.contributor.author | Inthachat W. | |
| dc.contributor.author | Laowanitwattana T. | |
| dc.contributor.author | Buacheen P. | |
| dc.contributor.author | Suttisansanee U. | |
| dc.contributor.author | Pitchakarn P. | |
| dc.contributor.correspondence | Temviriyanukul P. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2026-10-01T18:49:17Z | |
| dc.date.available | 2026-10-01T18:49:17Z | |
| dc.date.issued | 2026-09-01 | |
| dc.description.abstract | Wolffia globosa, the world’s smallest flowering plant, is a sustainable protein- and phytochemical-rich food source with emerging neuroprotective potential. This study presents the first comprehensive characterization that integrates extraction optimization, multitarget bioactivity profiling, drug synergy assessment, high-resolution metabolomics, molecular docking, and in vivo validation in Drosophila melanogaster. Ethanol-based extraction was optimized using a Box–Behnken design and response surface methodology (RSM), yielding optimal conditions of 32% ethanol, 1:40 (g/mL) solid-to-solvent ratio, 60 °C, and 28 min. The optimized extract exhibited a total phenolic content (TPC) of 15.17 ± 0.27 mg GAE/g DW, a total flavonoid content (TFC) of 22.34 ± 1.71 mg QE/g DW, and an exceptional ORAC antioxidant activity of 4374.33 ± 395.65 µmol TE/g DW. Potent and selective BACE-1 inhibition was observed (IC<inf>50</inf>: 1.59 ± 0.11 mg/mL), alongside moderate AChE (IC<inf>50</inf>: 7.42 mg/mL) and BChE (IC<inf>50</inf>: 6.55 mg/mL) inhibition. Synergistic interactions with donepezil were confirmed by the Chou–Talalay combination index method, with combined AChE, BChE, and BACE-1 inhibitions reaching 60.3%, 77.0%, and 82.2%, respectively—substantially exceeding theoretical additive values. Multi-platform metabolite profiling by HPLC-QTOF-MS/MS and LC-ESI-MS/MS identified luteolin, apigenin, caffeic acid, isovitexin, schaftoside, and pinolenic acid as the principal bioactives. Molecular docking predicted favorable binding of luteolin (delta-G: −10.24 kcal/mol, AChE) and naringenin (delta-G: −8.76 kcal/mol, BACE-1) against crystal structures of human AChE (PDB: 7E3H), BChE (PDB: 4TPK), and BACE-1 (PDB: 6EQM). In vivo, the W. globosa extract significantly improved locomotor performance and suppressed brain BACE-1 activity in an Drosophila AD model over 28 days. These findings establish W. globosa as a multifunctional nutraceutical candidate for neurodegenerative disease prevention. | |
| dc.identifier.citation | International Journal of Molecular Sciences Vol.27 No.18 (2026) | |
| dc.identifier.doi | 10.3390/ijms27188266 | |
| dc.identifier.eissn | 14220067 | |
| dc.identifier.issn | 16616596 | |
| dc.identifier.scopus | 2-s2.0-105051560888 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/119339 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Chemical Engineering | |
| dc.subject | Chemistry | |
| dc.subject | Biochemistry, Genetics and Molecular Biology | |
| dc.subject | Computer Science | |
| dc.title | Optimization and Metabolomic Profiling of Wolffia globosa Extract Reveal Multitarget Neuroprotective Activity Against Alzheimer’s Disease with In Vitro, In Silico, and In Vivo Validation | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105051560888&origin=inward | |
| oaire.citation.issue | 18 | |
| oaire.citation.title | International Journal of Molecular Sciences | |
| oaire.citation.volume | 27 | |
| oairecerif.author.affiliation | Mahidol University | |
| oairecerif.author.affiliation | Faculty of Medicine, Chiang Mai University |
