Evaluation of Umbelliferone Neuroprotective Effects Against Acrylamide-Induced Oxidative Stress, In Vivo and In Silico Study.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Evaluation of Umbelliferone Neuroprotective Effects Against Acrylamide-Induced Oxidative Stress, In Vivo and In Silico Study.
Συγγραφείς: Mogadem A; Department of Chemistry, College of Science, Taibah University, Madinah, Saudi Arabia. amogadam@taibahu.edu.sa., Al-Refai HH; Department of Chemistry, College of Science in Yanbu, Taibah University, Yanbu Governorate, Saudi Arabia.
Πηγή: Journal of molecular neuroscience : MN [J Mol Neurosci] 2026 Jun 10; Vol. 76 (2). Date of Electronic Publication: 2026 Jun 10.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Humana Press Country of Publication: United States NLM ID: 9002991 Publication Model: Electronic Cited Medium: Internet ISSN: 1559-1166 (Electronic) Linking ISSN: 08958696 NLM ISO Abbreviation: J Mol Neurosci Subsets: MEDLINE
Imprint Name(s): Publication: Totowa, NJ : Humana Press
Original Publication: Boston : Birkhäuser [i.e. Cambridge, MA : Birkhäuser Boston, c1989-
Ιατρικοί όροι (MeSH): Umbelliferones*/pharmacology , Umbelliferones*/therapeutic use , Acrylamide*/toxicity , Neuroprotective Agents*/pharmacology , Neuroprotective Agents*/therapeutic use , Antioxidants*/pharmacology , Antioxidants*/therapeutic use , Oxidative Stress*, Tumor Necrosis Factor-alpha/metabolism ; Tumor Necrosis Factor-alpha/genetics ; Liver/drug effects ; Liver/metabolism ; Heme Oxygenase-1/metabolism ; Heme Oxygenase-1/genetics ; Caspase 3/metabolism ; Caspase 3/genetics ; Brain/metabolism ; Brain/drug effects ; Alanine Transaminase/metabolism ; Animals ; Mice ; Male ; Molecular Docking Simulation ; Lipid Peroxidation
Περίληψη: Acrylamide (ACR) is a heat-generated carcinogen, one of the most common toxins, with various effects on the biological system, including oxidative stress and related disorders. Umbelliferone (UMB) is a naturally occurring coumarin derivative that is present in edible fruits, known as an antioxidant, and reported for many other therapeutic effects. In the current study, UMB was evaluated for neuro- and hepatoprotective activity against oxidative stress toxicity induced by a 40 mg/kg daily dose of ACR in a mouse model over 15 days. Also, UMB was used as a ligand for the first time to predict its affinity for the most important proteins involved in neuronal failure. The UMB administration significantly improves liver enzyme elevations, alanine transaminase (ALT) and aspartate transaminase (AST), following ACR injection. Also, UMB treatment reduced elevated total protein (TP) and albumin (ALB) serum levels. In addition, lipid peroxidation levels were significantly reduced by UMB (expressed as malondialdehyde MDA levels), and the levels of total non-enzymatic antioxidant capacity (TAC) were increased in brain tissue homogenate in comparison with brain injury in the ACR group. Furthermore, UMB downregulated the expression of tumor necrosis factor-alpha (TNF-α), an inflammatory marker and caspase-3, an apoptotic marker, while upregulating heme oxygenase-1 (HO-1), an antioxidant enzyme, in both liver and brain tissues. Molecular docking analysis revealed that the compound could form H-bonds and hydrophobic interactions with the target receptors. Results of this study conclude that UMB may be considered a potential pharmaceutical agent to ameliorate ACR-induced toxicity in the liver and brain, due to its anti-inflammatory, antioxidant, and antiapoptotic mechanisms, as well as its moderate affinity for neuronal disease-targeted proteins.
(© 2026. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
Competing Interests: Declarations. Competing interests: The authors declare no competing interests.
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Contributed Indexing: Keywords: Acrylamide; Caspase-3; Hemeoxygenase-1; Hepatoprotective; Molecular docking; Neuroprotective; Oxidative stress; Umbelliferone
Substance Nomenclature: 0 (Umbelliferones)
20R035KLCI (Acrylamide)
0 (Neuroprotective Agents)
60Z60NTL4G (7-hydroxycoumarin)
0 (Tumor Necrosis Factor-alpha)
0 (Antioxidants)
EC 1.14.14.18 (Heme Oxygenase-1)
EC 3.4.22.- (Caspase 3)
EC 2.6.1.2 (Alanine Transaminase)
Entry Date(s): Date Created: 20260610 Date Completed: 20260612 Latest Revision: 20260706
Update Code: 20260706
DOI: 10.1007/s12031-026-02555-4
PMID: 42268355
Βάση Δεδομένων: MEDLINE
Περιγραφή
ISSN:1559-1166
DOI:10.1007/s12031-026-02555-4