4.7 Article

Aegle marmelos Leaf Extract Phytochemical Analysis, Cytotoxicity, In Vitro Antioxidant and Antidiabetic Activities

Journal

PLANTS-BASEL
Volume 10, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/plants10122573

Keywords

Aegle marmelos; HepG(2) cells; GC; MS; HPLC; diabetes; cytotoxicity; antioxidant

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Funding

  1. Taif University, Taif, Saudi Arabia [TURSP-2020/124]

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Aegle marmelos leaf extract exhibited strong cytotoxicity and antioxidant potential, with the ability to reduce ROS levels caused by high glucose and enhance glucose uptake. The study also identified significant inhibitory effects on alpha-amylase and alpha-glycosidase enzymes, suggesting potential as a therapeutic agent for diabetes and related diseases.
For many years, Aegle marmelos (A. marmelos) has been used medicinally and as a dietary supplement. Despite this, there are minimal research data on A. marmelos phytochemical properties and pharmacological effects. This study aimed to explore the phytoconstituents, cytotoxicity, glucose uptake, and antioxidant and antidiabetic potential of an alcoholic extract of A. marmelos leaf. The cytotoxicity of A. marmelos in HepG2 cells was tested in vitro, and the results revealed that it has strong cytocompatibility and cytoprotective properties. The extract's antioxidant activities were investigated using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP) methods. Antioxidant potential was shown to be quite impressive. The enzymes alpha-amylase and alpha-glycosidase were found to be substantially inhibited by A. marmelos, with IC50 values of 46.21 and 42.07 mg/mL, respectively. In HepG2 cells, A. marmelos significantly reduced ROS levels that were elevated due to high glucose and enhanced glucose consumption (p < 0.05). These activities might be due to the enrichment of bioactive phytoconstituents analyzed chromatographically using GC/MS and HPLC. The findings of this study show that A. marmelos could be an effective restorative therapy for diabetes and related diseases.

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