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Natural flavonoids are potent inhibitors of glycogen phosphorylase

✍ Scribed by Sandra Jakobs; Diana Fridrich; Sabine Hofem; Gudrun Pahlke; Gerhard Eisenbrand


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
742 KB
Volume
50
Category
Article
ISSN
1613-4125

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✦ Synopsis


Abstract

There is little known about effects to be expected from high intake of flavonoids with respect to regulation of glucose/glycogen homeostasis. Glucose/glycogen homeostasis is mainly regulated by glycogen synthase (GS) and glycogen phosphorylase (GP). We investigated effects of naturally occurring flavonoids with varying substitution pattern on the activity of isolated muscle GP. Almost all flavonoids tested inhibited phosphorylated, active GPa, as well as unphosphorylated, adenosine monophosphate‐activated GPb. However, inhibition of GPa was two‐to‐fourfold stronger than that of GPb. The flavonol quercetin and the anthocyanidins cyanidin and delphinidin turned out to be the most potent inhibitors of GPa, with concentration values where enzymatic activity is 50% of the respective control in the low micromolar range (<Β 5 ΞΌM). Furthermore, by comparing GPa inhibitory activity of typical representatives from all known flavonoid classes, structural elements of flavonoids required for effective GP inhibition could be identified.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Stereospecific Synt
✍ T. M. KRUELLE; C. DE LA FUENTE; K. A. WATSON; M. GREGORIOU; L. N. JOHNSON; K. E. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 1 views

Stereospecific Synthesis of Spirohydantoins of Ξ²-Glucopyranose: Inhibitors of Glycogen Phosphorylase. -The key intermediate in the synthesis of title compounds (VIII), the bicyclic lactone (V), is readily prepared from azidolactone (I) (or its Ξ±-azido isomer). The rigid structure of (V) guarantees