Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2011; Volume 203, Supplement 688
The 62nd National Congress of the Italian Physiological Society
9/25/2011-9/27/2011
Sorrento, Italy


ROLE OF FLAVONOLS AND FLAVAN-3OLS IN CA2+ HOMEOSTASIS BY INCREASING THE SUPEROXIDE PRODUCTION
Abstract number: P10

LA GUARDIA1 M, DI MAJO1 D, CINQUEMANI1 GM, GIAMMANCO1 M

1Dept DISMOT, Univ. of Palermo, Palermo, Italy

Background: 

Ca2+ signalling is very sensitive to oxidants or reducing agents; changes in the redox state result in relevant changes in Ca2+ homeostasis, either altering Ca2+ mobilization from the internal stores and Ca2+ entry from the extracellular medium or modulating the activity of Ca2+ "off"mechanisms, including Ca2+ pumps and exchangers. In cardiac, smooth, and skeletal muscles ROS induce Ca2+ release via modifications in D-myo-inositol 1,4,5-trisphosphate (IP3)-induced Ca2+ release. it has been reported that stimulates IP3-induced Ca2+ release from the SR of vascular smooth muscle.

Aim: 

Of this study was to investigate whether four flavanoids: quercetin, kaempferol, (+) catechin and (-) epicatechin are able to increase the superoxide anion production modulating the activity of MnSOD. In order to underline a role of these molecules in Ca2+ homeostasis.

Method: 

The SOD modulation activity was monitored with a spectrophotometric assay using the xantina/xantina oxidase(XO)-XTT system. The molecule concentrations ranged from 1 to 100 mM for each.

Results: 

Quercetin and kaempferol increase the rate of superoxide generation at lower concentrations (<10mM). Instead, they become inhibitors of the enzyme when increasing in concentration (100-150mM). Catechin and epicatechin are activators of SOD or radical scavengers at lower concentrations (<= 25mM).

Conclusion: 

We hypothesize that flavonoids could induce relevant changes in Ca+2 homeostasis by increasing the superoxide production.

To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 203, Supplement 688 :P10

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE