LC/MS-MS Analysis of Phenolic Compounds in Hyoscyamus albus L. Extract: In Vitro Antidiabetic Activity, In Silico Molecular Docking, and In Vivo Investigation against STZ-Induced Diabetic Mice

dc.contributor.authorKenza Kadi
dc.date.accessioned2024-02-28T14:33:04Z
dc.date.available2024-02-28T14:33:04Z
dc.date.issued2023
dc.description.abstractThis study aimed to investigate the chemical composition and antidiabetic properties of cultivated Hyoscyamus albus L. The ethanol extract was analyzed using LC-MS/MS, and 18 distinct phenolic compounds were identified. Among these, p-coumaric acid (6656.8 3.4 g/g), gallic acid (6516 1.7 g/g), luteolin (6251.9 1.3 g/g), apigenin (6209.9 1.1 g/g), and rutin (5213.9 1.3 g/g) were identified as the most abundant polyphenolic molecules. In the in vitro antidiabetic experiment, the ability of the plant extract to inhibit -glucosidase and -amylase activities was examined. The results indicated that the extract from H. albus L. exhibited a higher inhibitory effect on -amylase compared to -glucosidase, with an IC50 of 146.63 1.1 g/mL and 270.43 1.1 g/mL, respectively. Docking simulations revealed that luteolin, fisetin, and rutin exhibited the most promising inhibitory activity against both enzymes, as indicated by their high contrasting inhibition scores. To further investigate the in vivo antidiabetic effects of H. albus L., an experiment was conducted using STZ-induced diabetic mice. The results demonstrated that the plant extract effectively reduced the levels of cholesterol and triglycerides. These findings suggest that H. albus L. may have therapeutic potential for managing hyperlipidemia, a common complication associated with diabetes. This highlights its potential as a natural remedy for diabetes and related conditions.
dc.identifier.urihttp://dspace.univ-khenchela.dz:4000/handle/123456789/2307
dc.language.isoen
dc.publisherSee discussions, stats, and author profiles for this publication
dc.titleLC/MS-MS Analysis of Phenolic Compounds in Hyoscyamus albus L. Extract: In Vitro Antidiabetic Activity, In Silico Molecular Docking, and In Vivo Investigation against STZ-Induced Diabetic Mice
dc.typeArticle
Files
Original bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
SabrinaPharmaceuticalsJuly2023.pdf
Size:
1.68 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed to upon submission
Description: