GC-MS Analysis, Antioxidant, and Antidiabetic Properties of Methanol Extract of Annona muricata L. Leaves - An In vitro and In silico Study

Author:

Mishra Abhay Prakash1,Nigam Manisha2,Nambooze Jennifer3,Salau Veronica F.1,Olofinsan Kolawole A.14,Iriti Marcello56,Matsabisa Motlalepula G.1

Affiliation:

1. Department of Pharmacology, University of Free State, Bloemfontein 9300, South Africa

2. Department of Biochemistry, H.N.B. Garhwal University, Srinagar, Garhwal, Uttarakhand 246174, India

3. Department of Chemistry, University of Free State, Bloemfontein 9300, South Africa;

4. Department of Biochemistry, School of Life Sciences, University of KwaZulu-Natal Westville Campus, Durban 4000, South Africa

5. Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano, Milan 20133, Italy

6. National Interuniversity Consortium of Materials Science and Technology, Firenze 50121, Italy

Abstract

Abstract: The Annona muricata L. leaves have been long employed in the traditional remedy of diabetes mellitus (DM) and its comorbidities. Different analytical techniques were used to evaluate the methanol extract of this plant part. In vitro antidiabetic assays of A. muricata extract were analysed using α-glucosidase and α-amylase inhibition tests. Employing gas chromatography-mass spectrometry (GC-MS), the primary bioactive components of the methanol extract were identified. Additionally, molecular docking experiments regarding the identified compounds were performed by silicification of UCFS Chimera, Autodock Vina, and BIOVIA Discovery Studio software. The total phenolic content of the A. muricata leaf extract was 14.83 mg GAE/g and the total flavonoids 34.22 mg QE/g. The plant extract showed concentration-dependent ferric reducing antioxidant power (FRAP) when compared with the standard ascorbic acid whereas significant radical scavenging activity was exhibited through the 2,2-Diphenyl-1-picrylhydrazyl (DPPH•) assay with IC50 of 0.202 μg/mL. Ten compounds were revealed by GC-MS analysis, and they exhibited a favourable quantity (area %). The extract inhibited α-amylase enzymes with a range of 36.52% - 67.30% as well as α-glucosidase enzymes with a range of 42.68 - 72.80% at different doses (15 μg/mL - 240 μg/mL) and performed well compared to the conventional drug acarbose. The high binding affinity of plant phytochemicals to α-amylase and α-glucosidase and their acceptable pharmacokinetic characteristics further suggested a prospective therapeutic relevance. According to our investigations, the leaves of A. muricata can be used to develop drugs with high antioxidant potential. However, adequate scientific data is needed for A. muricata's therapeutic use, as well as further clinical and in vivo research both for toxicological and pharmacological evaluation.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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