Investigating of the Phytoconstituents, Anti‐ <i>α</i> ‐Glucosidase, Antilipase, Anti‐ <i>α</i> ‐Amylase, and DPPH Radical Scavenging Activities of Extracts From <i>Eriobotrya japonica</i>
Recent research reported inhibitory effects of <i>Eriobotrya japonica</i> leaf extracts on DPPH free radicals and <i>α</i>-amylase, <i>α</i>-glucosidase, and lipase enzymes. These enzymes were linked to the etiology of diabetes mellitus, obesity, and oxidative stress. The current study is aimed at determining the phytocontents of <i>E. japonica</i> aqueous extract leaves and exploring their potential antioxidant, anti-<i>α</i>-amylase, anti-<i>α</i>-glucosidase, and antilipase activity using reference phytochemical and biochemical assays. The phytochemical tests on the <i>E. japonica</i> aqueous extract confirmed the presence of alkaloids, glycosides, tannins, saponins, phytosteroids, carbohydrates, and phenols. The total phenol and tannin contents of the <i>E. japonica</i> aqueous extract were 21.64 ± 0.89 mg of GAE/g and 1.72 ± 1 mg of CAE/g, respectively. <i>E. japonica</i> aqueous extract had inhibitory effects on DPPH free radicals (IC<sub>50</sub> of 7.7 ± 3.11 <i>μ</i>g/mL) and <i>α</i>-amylase (IC<sub>50</sub> = 141 ± 0.35 <i>μ</i>g/mL) compared with Trolox and acarbose (6.3 ± 0.12 and 28.18 ± 1.22 <i>μ</i>g/mL, respectively). Moreover, <i>E. japonica</i> aqueous extract inhibited <i>α</i>-glucosidase (IC<sub>50</sub> = 39.81 ± 0.74 vs. 37.15 ± 0.33 <i>μ</i>g/mL inhibition by acarbose) and lipase (IC<sub>50</sub> = 316.2 ± 0.87 vs. 12.3 ± 0.33 <i>μ</i>g/mL inhibition by orlistat). In conclusion, the current results suggest that <i>E. japonica</i> aqueous extract possesses strong antioxidant, anti-<i>α</i>-glucosidase, anti-<i>α</i>-amylase, and antilipase activities with potential applications in the treatment and prevention of obesity, diabetes mellitus, and oxidative stress.
Authors
- Majdi Dwikat (ORCID: https://orcid.org/0000-0001-6365-7622)
- Mustafa Ghanim (ORCID: https://orcid.org/0000-0003-3258-3530)
- Johnny Amer (ORCID: https://orcid.org/0000-0001-5828-6783)
- Mohammed Hawash (ORCID: https://orcid.org/0000-0001-5640-9700)
- Maha Rabayaa (ORCID: https://orcid.org/0000-0002-8702-5213)
- Malik Alqub (ORCID: https://orcid.org/0000-0002-7374-177X)
- Mohammad Abuawad (ORCID: https://orcid.org/0009-0000-7924-8786)
- Nidal Jaradat (ORCID: https://orcid.org/0000-0003-2291-6821)
- Linda Issa (ORCID: https://orcid.org/0000-0001-8509-826X)
- Belal Rahhal (ORCID: https://orcid.org/0000-0002-6650-3087)
- Fatimah Hussein (ORCID: https://orcid.org/0000-0001-7066-2411)
- Mohammad Halayqa
- Wad Zaghloul
- Esraa Hamdan
Institutions
- An-Najah National University (PS)
Publication Details
- Journal
- BioMed Research International
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1155/bmri/8888528
- Primary Topic
- Natural product bioactivities and synthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00