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Acta Physiologica Congress

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Acta Physiologica 2010; Volume 200, Supplement 681
Abstracts of the 61st National Congress of the Italian Physiological Society
9/15/2010-9/17/2010
Varese, Italy


MECHANISM OF ACTION OF THE BETALAIN PIGMENT INDICAXANTHIN, PURIFIED FROM FRUITS OF OPUNTIA FICUS-INDICA, ON MOUSE ILEAL MOTILITY IN VITRO
Abstract number: P85

BALDASSANO1 S, ROTONDO1 A, TESORIERE2 L, LIVREA2 MA, MULE1 F

1Dipartimento di Biologia cellulare e dello Sviluppo e
2Dipartimento Farmacochimico Tossicologico Biologico, Universit di Palermo, Palermo, Italy

Betalains, such us indicaxanthin and betacyanins,are nitrogenous pigments present in fruits of many caryophyllales, like Opuntia ficus indica,with potent antioxidant proprieties. However, their biological activities are poorly known. Previously weshowed that the Opuntia ficus indica fruit extract (OFE)induced a concentration-dependent reduction of spontaneous and evoked mechanical activity of mouse ileum, which was mimicked by its pigment indicaxanthin.Therefore, the purpose of this study was to examinethe indicaxanthin mechanism of action, in mouse ileum longitudinal muscle, using organ bath technique.

The inhibitory action of indicaxanthin (3–100 mM) on spontaneous mechanical activity was unaffected by indomethacin (10 mM), inhibitor of cycloxygenase, ODQ (10 mM), selective inhibitor of nitric oxide-dependent guanylyl cyclase, and DDA (10 mM), adenylate cyclase inhibitor, while it was significantly reduced in the presence of IBMX (10 mM), a non selective inhibitor of phosphodiesterases (PDEs). In addition indicaxanthin, as IBMX, increased the inhibitory effects of foskolin (1 nM – 1 mM), an adenylate cyclase activator, while it did not affect the inhibitory action of sodium nitroprusside (1 –100 mM), a soluble guanylil cyclase activator, which was increased only by IBMX. The present data show for the first time that indicaxanthin from OFE is able to reduce the contractility of ileal longitudinal muscle by inhibition of PDEs and likely increase of intracellular cAMP.

To cite this abstract, please use the following information:
Acta Physiologica 2010; Volume 200, Supplement 681 :P85

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