Physiological concentrations of zinc have dual effects on P2X myenteric receptors of guinea pig

"We, hereby, characterize the pharmacological effects of physiological concentrations of Zinc on native myenteric P2X receptors from guinea-pig small intestine and on P2X2 isoforms present in most myenteric neurons. This is the first study describing opposite effects of Zinc on these P2X recept...

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Detalles Bibliográficos
Autores: Liliana Hortencia Méndez Barredo, JESSICA GABRIELA RODRIGUEZ MELENDEZ, KAREN SARAHI GOMEZ CORONADO, Raquel Guerrero Alba, Eduardo Emmanuel Valdez Morales, ROSA ESPINOSA LUNA, ALMA ROSA BARAJAS ESPINOSA, Carlos Barajas López
Tipo de recurso: artículo
Estado:Versión enviada para evaluación y publicación
Fecha de publicación:2018
País:México
Institución:Instituto Potosino de Investigación Científica y Tecnológica
Repositorio:Repositorio Institucional del IPICYT
OAI Identifier:oai:ipicyt.repositorioinstitucional.mx:1010/2086
Acceso en línea:http://ipicyt.repositorioinstitucional.mx/jspui/handle/1010/2086
Access Level:acceso abierto
Palabra clave:info:eu-repo/classification/Autor/Myenteric neurons
info:eu-repo/classification/Autor/Gastrointestinal tract
info:eu-repo/classification/Autor/ATP
info:eu-repo/classification/Autor/Zinc
info:eu-repo/classification/Autor/P2X2 recombinant receptors
info:eu-repo/classification/Autor/P2X native receptors
info:eu-repo/classification/cti/2
info:eu-repo/classification/cti/24
info:eu-repo/classification/cti/2415
Descripción
Sumario:"We, hereby, characterize the pharmacological effects of physiological concentrations of Zinc on native myenteric P2X receptors from guinea-pig small intestine and on P2X2 isoforms present in most myenteric neurons. This is the first study describing opposite effects of Zinc on these P2X receptors. It was not possible to determine whether both effects were concentration dependent, yet the inhibitory effect was mediated by competitive antagonism and was concentration dependent. The potentiating effect appears to be mediated by allosteric changes induced by Zinc on P2X myenteric channels, which is more frequently observed in myenteric neurons with low zinc concentrations. In P2X2-1 and P2X2-2 variants, the inhibitory effect is more common than in P2X myenteric channels. However, in the variants, the potentiatory effect is of equal magnitude as the inhibitory effect. Inhibitory and potentiatory effects are likely mediated by different binding sites that appear to be present on both P2X2 variants. In conclusion, in myenteric native P2X receptors, Zinc has quantitatively different pharmacological effects compared to those observed on homomeric channels: P2X2-1 and P2X2-2. Potentiatory and inhibitory Zinc effects upon these receptors are mediated by two different binding sites. All our data suggest that myenteric P2X receptors have a more complex pharmacology than those of the recombinant P2X2 receptors, which is likely related to other subunits known to be expressed in myenteric neurons. Because these dual effects occur at Zinc physiological concentrations, we suggest that they could be involved in physiological and pathological processes."