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Flavonoids isolated from Syzygium aqueum leaf extract as potential antihyperglycaemic agents
Authors:Thamilvaani Manaharan  David Appleton  Hwee Ming Cheng  Uma D Palanisamy
Affiliation:1. Department of Physiology, Faculty of Medicine, University of Malaya, 59100 Kuala Lumpur, Malaysia;2. Department of Pharmacology, Faculty of Medicine, University of Malaya, 59100 Kuala Lumpur, Malaysia;3. School of Medicine and Health Sciences, Monash University, Sunway Campus, 46150 Bandar Sunway, Malaysia
Abstract:Syzygium aqueum is a medicinal plant which is grown in tropical regions. In this study, the ethanolic extracts of S. aqueum leaf were investigated for its antihyperglycaemic activity. Our investigation revealed its effectiveness in inhibiting the carbohydrate hydrolysing enzymes, α-glucosidase (EC50 = 11 μg/ml) and α-amylase (EC50 = 8 μg/ml), at significant level than the commercial drug acarbose (EC50 = 28 μg/ml, α-glucosidase; EC50 = 12 μg/ml, α-amylase). In addition, the ethanolic leaf extracts were able to inhibit the key enzyme in the polyol pathway, aldose reductase (EC50 = 0.03 μg/ml) and prevent the AGEs formation by 89%. Six flavonoid compounds, 4-hydroxybenzaldehyde (1), myricetin-3-O-rhamnoside (2), europetin-3-O-rhamnoside (3), phloretin (4), myrigalone-G (5) and myrigalone-B (6), were isolated from the ethanolic leaf extracts. Compounds (2) and (3) showed high inhibitory activities, with EC50 values of 1.1 μM and 1.9 μM against α-glucosidase and EC50 values of 1.9 μM and 2.3 μM against α-amylase, respectively. These findings provide a strong rationale to establish S. aqueum’s capability as an antihyperglycaemic agent.
Keywords:Syzygium aqueum  α-Glucosidase inhibitor  α-Amylase inhibitor  Aldose reductase inhibitor  Advanced glycation end-products inhibitor
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