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Inhibitory Effects of Solvent-Partitioned Fractions of Two Nigerian Herbs ( Linn. and L.) on α-Amylase and α-Glucosidase. | LitMetric

Inhibitory Effects of Solvent-Partitioned Fractions of Two Nigerian Herbs ( Linn. and L.) on α-Amylase and α-Glucosidase.

Antioxidants (Basel)

Biotechnology and Structural Biology (BSB) Group, Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa 3886, South Africa.

Published: May 2018

Therapies directed towards controlling hyperglycemia, the hallmark of type-2 diabetes mellitus, go a long way in managing diabetes and its related complications. Reducing glucose level through the inhibition of the relevant carbohydrate hydrolyzing enzymes is one among many routes in the management of diabetes. This study investigates the enzyme inhibitory and antioxidant properties of solvent-partitioned fractions of and leaves; which are used extensively in the treatment of diabetic patients locally. The leaves of and were extracted with methanol and fractionated to obtain -hexane (HF), ethyl acetate (EAF), -butanol (BF), and aqueous (AF) fractions successively. The α-amylase and α-glucosidase inhibitory activities of fractions of and leaves were investigated while the antioxidant activity of each fraction was analyzed using iron chelating and ABTS (2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulphonic acid) radical scavenging assay. Our findings indicated that the ethyl acetate fraction of leaves contained a considerably higher ( < 0.05) amount of total phenolic, flavonoids, metal ion, and ABTS radical scavenging activity than the ethyl acetate fractions of . Furthermore, the ethyl acetate fraction of had a considerably higher ( < 0.05) inhibitory effect on α-glucosidase (IC = 25.11 ± 0.01 μg mL), and α-amylase (IC = 24.04 ± 0.12 μg mL) activities than the fraction. Hence, the inhibitory activities of and leaves suggest that they are a potential source of orally active antidiabetic agents and could be employed to formulate new plant-based pharmaceutical and nutraceutical drugs to improve human health.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025479PMC
http://dx.doi.org/10.3390/antiox7060073DOI Listing

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