Pinoresinol diglucoside is screened as a putative α-glucosidase inhibiting compound in Actinidia arguta leaves
Actinidia arguta leaves are consumed as a popular food material in Korea and have been reported to exert beneficial effects on humans due to its constituent polyphenolic compounds. In this study, the α-glucosidase inhibitory compounds in A. arguta were screened and identified through α-glucosidase-g...
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| Published in | Applied biological chemistry Vol. 57; no. 4; pp. 473 - 479 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Seoul
The Korean Society for Applied Biological Chemistry
01.08.2014
Springer Nature B.V 한국응용생명화학회 |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1738-2203 2468-0834 2234-344X 2234-344X 2468-0842 |
| DOI | 10.1007/s13765-014-4167-0 |
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| Summary: | Actinidia arguta
leaves are consumed as a popular food material in Korea and have been reported to exert beneficial effects on humans due to its constituent polyphenolic compounds. In this study, the α-glucosidase inhibitory compounds in
A. arguta
were screened and identified through α-glucosidase-guided fractionation and metabolomic analysis. The 50% ethanol extracts of
A. arguta
showed strong inhibitory effect (32.6%), which was comparable to acarbose as a positive control (30.0%). Through multiple steps of fractionation, pinoresinol diglucoside and fertaric acid were identified as the major potent compounds in
A. arguta
inhibiting α-glucosidase activity by liquid chromatography mass spectrometry analysis and metabolomic comparison. Particularly, because pinoresinol and its glycosides have been demonstrated as α-glucosidase inhibitory agents, pinoresinol diglucoside was proposed to be a putative key compound for α-glucosidase inhibition in
A. arguta
. This is the first study demonstrating the anti-diabetic effect of a pinoresinol-containing fraction of
A. arguta
and would be useful for its application as a natural α-glucosidase inhibitor. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 G704-000111.2014.57.4.009 |
| ISSN: | 1738-2203 2468-0834 2234-344X 2234-344X 2468-0842 |
| DOI: | 10.1007/s13765-014-4167-0 |