کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2910118 | 1174605 | 2011 | 5 صفحه PDF | دانلود رایگان |

In this study, the interactions of free and bound phenolic-rich extracts from shaddock peels (popular in folklore for the management of diabetes and hypertension) with α-amylase and α-glucosidase (key enzymes linked to type-2 diabetes) and angiotensin I-converting enzyme (ACE) (key enzyme linked to hypertension) were assessed. The free phenolics of shaddock (Citrus maxima) peels were extracted with 80% acetone, while the bound phenolics were extracted from the alkaline and acid hydrolyzed residue with ethyl acetate; and their interaction with the enzymes were assessed. The phenolic extracts inhibited α-amylase, α-glucosidase and ACE enzyme activities in a dose-dependent manner; however, bound phenolics had significantly higher (P < 0.05) α-amylase inhibitory activities, than free phenolics, which had significantly higher (P < 0.05) ACE inhibitory activities. There was no significant difference (P > 0.05) in their α-glucosidase inhibitory activities. The stronger inhibition of α-glucosidase when compared to α-amylase is of great pharmaceutical importance. The phenolic inhibited sodium nitroprusside induced lipid peroxidation in pancreas in a dose dependent manner. Therefore, free and bound phenolic extracts from shaddock peels could be used as nutraceutical for the management of hypertension and type-2 diabetes.
► The interactions of free and bound phenolic-rich extracts from shaddock peels with α-amylase, α-glucosidase and angiotensin I-converting enzyme (ACE) were assessed.
► The phenolic extracts inhibited α-amylase, α-glucosidase and ACE enzyme activities in a dose-dependent manner.
► The phenolics inhibited sodium nitroprusside induced lipid peroxidation in pancreas in a dose dependent manner.
► Therefore, free and bound phenolic extracts from shaddock peels could be used as nutraceutical for the management of hypertension and type-2 diabetes.
Journal: Diabetes & Metabolic Syndrome: Clinical Research & Reviews - Volume 5, Issue 3, July–September 2011, Pages 148–152