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dc.contributor.authorJiménez-Pompa, Amanda
dc.contributor.authorSanz-Lázaro, Sara
dc.contributor.authorHone, Arik J.
dc.contributor.authorRueda-Ruzafa, Lola
dc.contributor.authorMedina-Polo, José
dc.contributor.authorGonzález Enguita, María del Carmen 
dc.contributor.authorBlázquez, Jesús
dc.contributor.authorde los Ríos, Cristóbal
dc.contributor.authorMichael McIntosh, J.
dc.contributor.authorAlbillos Martínez, María Almudena 
dc.contributor.otherUAM. Departamento de Farmacologíaes_ES
dc.date.accessioned2022-02-25T12:45:41Z
dc.date.available2022-02-25T12:45:41Z
dc.date.issued2021-06-04
dc.identifier.citationNeuropharmacology 195. (2021): 108632en_US
dc.identifier.issn0028-3908es_ES
dc.identifier.urihttp://hdl.handle.net/10486/700516
dc.description.abstractCardiovascular side effects of varenicline and a case report of a hypertensive crisis in a varenicline-prescribed patient with pheochromocytoma have been reported. The goal of the present study was to determine whether such side effects might derive, in part, from increased exocytosis of secretory vesicles and subsequent catecholamine release triggered by varenicline in human chromaffin cells of the adrenal gland. In this study, we performed electrophysiological plasma membrane capacitance and carbon fiber amperometry experiments to evaluate the effect of varenicline on exocytosis and catecholamine release, respectively, at concentrations reached during varenicline therapy (100 nM). Experiments were conducted in the absence or presence of nicotine, at plasma concentrations achieved right after smoking (250 nM) or steady-state concentrations (110 nM), in chromaffin cells of the adrenal gland obtained from human organ donors. Cells were stimulated with short pulses (10 ms) of acetylcholine (ACh; 300 μM) applied at 0.2 Hz, in order to closer mimic the physiological situation at the splanchnic nerve-chromaffin cell synapse. In addition, rat chromaffin cells were used to compare the effects obtained in cells from a more readily available species. Varenicline increased the exocytosis of secretory vesicles in human and rat chromaffin cells in the presence of nicotine, effects that were not due to an increase of plasma membrane capacitance or currents triggered by the nicotinic agonists alone. These results should be considered in nicotine addiction therapies when varenicline is useden_US
dc.description.sponsorshipThis work was supported by grants from the Spanish Ministry of Science and Innovation [grant number BFU2015-69092 to A.A.] and the U.S. National Institutes of Health [GM136430 and GM103801 to J.M.M]en_US
dc.format.extent11 pag.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.ispartofNeuropharmacologyen_US
dc.subject.otherAcetylcholine (PubChem CID: 187)en_US
dc.subject.otherChromaffin cellen_US
dc.subject.otherCytisine (PubChem CID: 597)en_US
dc.subject.otherDihydro-β-erythroidine (PubChem CID: 31762)en_US
dc.subject.otherDimethylphenylpiperazinium (PubChem CID: 1316)en_US
dc.subject.otherExocytosisen_US
dc.subject.otherHumanen_US
dc.subject.otherNicotineen_US
dc.subject.otherNicotine (PubChem CID: 89594)en_US
dc.subject.otherNicotinic receptoren_US
dc.subject.otherVareniclineen_US
dc.subject.otherVarenicline (PubChem CID:170361)en_US
dc.titleTherapeutic concentrations of varenicline increases exocytotic release of catecholamines from human and rat adrenal chromaffin cells in the presence of nicotineen_US
dc.typearticleen_US
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.neuropharm.2021.108632es_ES
dc.identifier.doi10.1016/j.neuropharm.2021.108632es_ES
dc.identifier.publicationfirstpage108632-1es_ES
dc.identifier.publicationissue195es_ES
dc.identifier.publicationlastpage108632-11es_ES
dc.identifier.publicationvolumeNeuropharmacologyes_ES
dc.relation.projectIDGobierno de España. BFU2015-69092es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimiento – NoComercial – SinObraDerivadaes_ES
dc.rights.accessRightsopenAccesses_ES
dc.authorUAMAlbillos Martínez, María Almudena (259007)
dc.facultadUAMFacultad de Medicina
dc.institutoUAMInstituto Teófilo Hernando de I+D del Medicamento (ITH)
dc.institutoUAMInstituto Ramón y Cajal de Investigación Sanitaria (IRYCIS)


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