Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/45306
DC FieldValueLanguage
dc.contributor.authorSanchez-Bueno, Antonioen_US
dc.contributor.authorGreenwood, Mark R.en_US
dc.contributor.authorVarela-Nieto, Isabelen_US
dc.contributor.authorMarrero Arencibia, María Isabelen_US
dc.contributor.authorGil, Beatrizen_US
dc.contributor.authorMato, Jose M.en_US
dc.contributor.authorCobbold, Peter H.en_US
dc.contributor.otherMATO, JOSE-
dc.contributor.otherVarela-Nieto, Isabel-
dc.contributor.otherMarrero-Arencibia, Isabel-
dc.date.accessioned2018-11-22T08:48:47Z-
dc.date.available2018-11-22T08:48:47Z-
dc.date.issued1997en_US
dc.identifier.issn0143-4160en_US
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/45306-
dc.description.abstractInositol-phosphoglycan (IPG) is a putative mediator of insulin action that has been shown to affect numerous biochemical processes. IPG, prepared from liver membranes, promptly inhibited phenylephrine- or vasopressin-induced [Ca2+]i oscillations when perfused over Fura-2-dextran injected rat hepatocytes. An antibody to IPG suppressed the inhibitory effect of insulin on the [Ca2+]i oscillations. Measurement of the rate of quench of cytoplasmic Fura-2 by extracellular Mn2+ showed that Ca2+ entry occurred continuously in the unstimulated cell and was not affected by phenylephrine or vasopressin. IPG, specifically, almost completely abolished the Mn2+ quench rate. Elevated extracellular [Ca2+] reversed the inhibitory effect of IPG on [Ca2+]i oscillations. We conclude that IPG inhibits the hepatocyte Ca2+ oscillatory by reducing the continuous Ca2+ influx that is required to sustain oscillations in [Ca2+]i.en_US
dc.languageengen_US
dc.relation.ispartofCell Calciumen_US
dc.sourceCell Calcium [ISSN 0143-4160], v. 21 (2), p. 125-133en_US
dc.subject32 Ciencias médicasen_US
dc.subject320502 Endocrinologíaen_US
dc.subject.otherInositol-phosphoglycanen_US
dc.subject.otherCalciumen_US
dc.subject.otherHepatocytesen_US
dc.titleInositol-phosphoglycan inhibits calcium oscillations in hepatocytes by reducing calcium entryen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0143-4160(97)90036-1en_US
dc.identifier.scopus2-s2.0-0031052584-
dc.identifier.isiA1997WL18200004-
dcterms.isPartOfCell Calcium-
dcterms.sourceCell Calcium[ISSN 0143-4160],v. 21 (2), p. 125-133-
dc.contributor.authorscopusid6701697888-
dc.contributor.authorscopusid7202445757-
dc.contributor.authorscopusid7004650477-
dc.contributor.authorscopusid35936487800-
dc.contributor.authorscopusid7103109287-
dc.contributor.authorscopusid55399368600-
dc.contributor.authorscopusid7006338359-
dc.description.lastpage133en_US
dc.description.firstpage125en_US
dc.relation.volume21en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:A1997WL18200004-
local.message.claim2022-07-07T13:46:37.822+0100|||rp01911|||submit_approve|||dc_contributor_author|||None*
dc.contributor.daisngid1934076-
dc.contributor.daisngid57514-
dc.contributor.daisngid294879-
dc.contributor.daisngid3844163-
dc.contributor.daisngid35147-
dc.contributor.daisngid26350-
dc.contributor.daisngid565660-
dc.identifier.investigatorRIDA-5187-2011-
dc.identifier.investigatorRIDG-5289-2015-
dc.identifier.investigatorRIDQ-9437-2016-
dc.description.numberofpages9en_US
dc.utils.revisionen_US
dc.date.coverdateFebrero 1997en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,265
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología-
crisitem.author.orcid0000-0003-3732-9929-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameMarrero Arencibia, María Isabel-
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