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J Nutr Biochem ; 21(3): 247-54, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19369059

RESUMEN

Caseinphosphopeptides (CPPs) are considered as mineral carriers because of their ability to bind and solubilize calcium ions, with the possible role, yet to be definitely assessed, of improving calcium absorption at the intestinal level. Previous works demonstrated that CPPs improve calcium uptake, with increasing intracellular calcium concentration, by human differentiated tumor HT-29 cells, and that this effect correlates with the supramolecular structure of CPPs in the presence of calcium ions. The aim of the present study was to establish whether the CPP effect on calcium uptake is specific for HT-29 cells and depends on the differentiated state of the cells. To this purpose, HT-29 and Caco2 cells, two models of intestinal cells, were differentiated following appropriate protocols, including treatment with 1,25-(OH)2 vitamin D3. The CPP-dependent intracellular calcium rises were monitored at the single-cell level through fura2-fluorescence assays, and cell differentiation was assessed by biochemical and morphological methods. Results clearly showed that the ability to take up extracellular calcium ions under CPP stimulation is exhibited by both HT-29 and Caco2 cells, but only upon cell differentiation. This evidence adds novel support to the notion that CPPs favour calcium absorption, thus possibly acting as cellular bio-modulators and carrying a nutraceutical potential.


Asunto(s)
Calcio/farmacocinética , Caseínas/farmacología , Diferenciación Celular/fisiología , Quelantes/farmacología , Mucosa Intestinal/efectos de los fármacos , Fragmentos de Péptidos/farmacología , Fosfopéptidos/farmacología , Fosfatasa Alcalina/metabolismo , Células CACO-2 , Calcitriol/farmacología , Calcio/farmacología , Señalización del Calcio/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Suplementos Dietéticos , Células HT29 , Humanos , Absorción Intestinal/efectos de los fármacos , Mucosa Intestinal/metabolismo , Mucosa Intestinal/ultraestructura , Cinética , Microvellosidades/enzimología , Complejo Sacarasa-Isomaltasa/metabolismo
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