In Vitro Experimental Assessment of Ethanolic Extract of Moringa oleifera Leaves as an α-Amylase and α-Lipase Inhibitor

Author:

Ogundipe Adebanke12,Adetuyi Babatunde3ORCID,Iheagwam Franklyn1ORCID,Adefoyeke Keleko4,Olugbuyiro Joseph5ORCID,Ogunlana Oluseyi6,Ogunlana Olubanke12ORCID

Affiliation:

1. Department of Biochemistry, Covenant University, Canaan Land, P.M.B 1023, Ota, Ogun State, Nigeria

2. Coveant Applied Informatics and Communication Africa Centre of Excellence, Covenant University, Canaan Land, P.M.B. 1023, Ota, Ogun State, Nigeria

3. Department of Natural Sciences, Biochemistry Unit, Precious Cornerstone University, Ibadan, Oyo State, Nigeria

4. Leady Pharma Industries Limited, Sango, Ota, Ogun State, Nigeria

5. Department of Industrial Chemistry, Covenant University, Canaan Land, P.M.B. 1023, Ota, Ogun State, Nigeria

6. Department of Biological Sciences, Crawford University, Igbesa, Ogun State, Nigeria

Abstract

Background and Objectives. Moringa oleifera has been scientifically reported to have effects on diabetes and obesity. An explanatory mechanism on how the plant exerts its enzyme inhibitory activities are yet to be detailed. This study was aimed at carrying out an in vitro assessment of ethanolic extracts (AEEs) of M. oleifera leaves for their antioxidant, antidiabetic, and antiobesity activities. Methods. Phytochemical screening, antioxidant activity, α-amylase, and α-lipase inhibitory assessment were carried out on Moringa oleifera extract. Results. The result of the phytochemical screening revealed the presence of total phenolic, flavonoid, tannin, and alkaloid contents of values 0.070 ± 0.005 mg gallic acid equivalent/g, 0.180 ± 0.020 mg rutin equivalent/g, 0.042 ± 0.001 mg tannic equivalent/g, and 12.17 ± 0.001%, respectively, while the total protein analysis was 0.475 ± 0.001 mg bovine serum albumin equivalent/g. Ferric reducing antioxidant power (FRAP) and total antioxidant capacity (TAC) values were 0.534 ± 0.001 mg gallic acid equivalent/g and 0.022 ± 0.00008 mg rutin equivalent/g, respectively. Diphenyl-2-picrylhydrazyl (DPPH), ABTS (2,2′-azino-bis (ethylbenzothiazoline-6-sulfonic acid)), and nitric oxide (NO) assays showed the extract to have a strong free radical scavenging activity. The 50% inhibitory concentration (IC50) values of the lipase and amylase activities of the extract are 1.0877 mg/mL and 0.1802 mg/mL, respectively. Conclusion. However, α-lipase and α-amylase inhibiting activity of M. oleifera could be related to the phytochemicals in the extract. This research validates the ethnobotanical use of M. oleifera leaves as an effective plant-based therapeutic agent for diabetes and obesity.

Publisher

Hindawi Limited

Subject

Biochemistry

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