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Am J Physiol Renal Physiol ; 281(6): F1075-81, 2001 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11704558

RESUMEN

Extracellular nucleotides are assumed to be important regulators of glomerular functions. This study characterizes purinergic receptors in podocytes. The effects of purinergic agonists on electrophysiological properties and the intracellular free Ca(2+) concentration of differentiated podocytes were examined with the patch-clamp and fura 2 fluorescence techniques. mRNA expression of purinergic receptors was investigated by RT-PCR. Purinergic agonists depolarized podocytes. Purinergic agonists similarly increased intracellular free Ca(2+) concentration of podocytes. The rank order of potency of various nucleotides on membrane voltage and free cytosolic calcium concentration was UTP approximately UDP > [adenosine 5'-O-(3-thiotriphosphate) (ATP-gamma-S)] > ATP > 2-methylthioadenosine 5'-triphosphate (2-MeS-ATP) > 2'- and 3'-O-(4-benzoylbenzoyl)-adenosine 5'-triphosphate (BzATP) > ADP-beta-S. alpha,beta-Me-ATP was without effect. In the presence of UTP, BzATP did not cause an additional depolarization of podocytes. Incubation of cells with ATP or BzATP did not induce lactate dehydrogenase release. In RT-PCR studies, mRNAs of the P2Y(1), P2Y(2), P2Y(6), and P2X(7) receptors were detected within glomeruli and podocytes. The data indicate that extracellular nucleotides modulate podocyte function mainly by an activation of both P2Y(2) and P2Y(6) receptors.


Asunto(s)
Glomérulos Renales/citología , Glomérulos Renales/fisiología , Nucleótidos/farmacología , Fosfato de Piridoxal/análogos & derivados , Receptores Purinérgicos P2/fisiología , Adenosina Trifosfato/farmacología , Animales , Calcio/metabolismo , Línea Celular Transformada , Cloruros/metabolismo , Relación Dosis-Respuesta a Droga , Conductividad Eléctrica , Espacio Extracelular/fisiología , Transporte Iónico , Ratones , Técnicas de Placa-Clamp , Antagonistas del Receptor Purinérgico P2 , Fosfato de Piridoxal/farmacología , ARN Mensajero/biosíntesis , Receptores de Leucotrieno B4 , Receptores Purinérgicos P2/genética , Suramina/farmacología
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