In Vitro Antioxidant and Alpha-glucosidase Inhibition Activity of Polygonatum verticillatum of Karnali, Nepal

Author:

Adhikari Achyut1ORCID,Shretha Dipesh2ORCID,Dhakal Kamal1ORCID,Pokhrel Tamlal1ORCID,Sharma Prabha2ORCID

Affiliation:

1. Central Department of Chemistry, Tribhuvan University, Kathmandu 44618, Nepal

2. Department of Chemistry, Tri-Chandra Multiple Campus, Tribhuvan University, Kathmandu 44605, Nepal

Abstract

Background: Diabetes mellitus is a metabolic disorder that has become a major health issue in the modern era due to long-term health consequences. α-amylase and α-glucosidase are the key enzymes involved in the digestion of starchy foods, and the inhibition of these enzymes is regarded as a postprandial hyperglycemia control strategy. Objective: The primary goal of this work is to examine the antioxidant activity as well as α- glucosidase inhibitory activity of Polygonatum verticillatum rhizomes via in vitro test. Method: The in vitro α-glucosidase inhibition activity was performed using p-nitrophenyl-α- Dglucopyranoside (PNPG) substrate. 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay was performed to estimate the antioxidant activity. Results: The in vitro α-glucosidase inhibitory activity of Polygonatum verticillatum was investigated for the very first time. Of the three fractions and a crude extract, the ethyl acetate (EA) fraction disclosed potent inhibition activity against α-glucosidase enzyme with an IC50 value of 22.3 ± 0.1 μg/mL. Likewise, the IC50 values for dichloromethane (DCM) fraction and the crude extract against α- glucosidase were reported at 34 ± 0.1 μg/mL and 402.2 ± 0.2 μg/mL, respectively. Similarly, the EA fraction, crude extract, and DCM fraction disclosed promising antioxidant activity with IC50 = 55 ± 0.3 μg/mL, 171.5 ± 0.6 μg/mL, and 164.1 ± 3.4 μg/mL, respectively. Conclusion: These findings concluded that among the crude extract and fractions of Polygonatum verticillatum of Nepalese origin, the EA fraction constituted a potent α-glucosidase inhibiting and antioxidant agent. Further research is required to expose the inhibiting compounds.

Funder

University Grants Commission (UGC), Nepal

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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