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

被引:2
|
作者
Mishra, Abhay Prakash [1 ]
Nigam, Manisha [2 ]
Nambooze, Jennifer [3 ]
Salau, Veronica F. [1 ]
Olofinsan, Kolawole A. [1 ,4 ]
Iriti, Marcello [5 ,6 ]
Matsabisa, Motlalepula G. [1 ]
机构
[1] Univ Free State, Dept Pharmacol, ZA-9300 Bloemfontein, South Africa
[2] HNB Garhwal Univ, Dept Biochem, Garhwal 246174, Uttarakhand, India
[3] Univ Free State, Dept Chem, ZA-9300 Bloemfontein, South Africa
[4] Univ Kwazulu Natal, Sch Life Sci, Dept Biochem, Westville Campus, ZA-4000 Durban, South Africa
[5] Univ Milan, Dept Biomed, Surg & Dent Sci, I-20133 Milan, Italy
[6] Natl Interuniv Consortium Mat Sci & Technol, I-50121 Florence, Italy
关键词
Annona muricata L; antidiabetic; enzyme inhibition; antioxidant; molecular docking; GC-MS analysis; METABOLISM;
D O I
10.2174/0113852728254495231002100354
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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 alpha-glucosidase and alpha-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 center dot) assay with IC50 of 0.202 mu g/mL. Ten compounds were revealed by GC-MS analysis, and they exhibited a favourable quantity (area %). The extract inhibited alpha-amylase enzymes with a range of 36.52% - 67.30% as well as alpha-glucosidase enzymes with a range of 42.68 - 72.80% at different doses (15 mu g/mL - 240 mu g/mL) and performed well compared to the conventional drug acarbose. The high binding affinity of plant phytochemicals to alpha-amylase and alpha-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.
引用
收藏
页码:1531 / 1541
页数:11
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