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dc.contributor.authorMetta Pinthongen_US
dc.contributor.authorStefanie A G Blacken_US
dc.contributor.authorFabiola M. Ribeiroen_US
dc.contributor.authorChumpol Pholpramoolen_US
dc.contributor.authorStephen S G Fergusonen_US
dc.contributor.authorRebecca Jane Ryletten_US
dc.contributor.otherWestern Universityen_US
dc.contributor.otherRobarts Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-12T02:51:34Z-
dc.date.available2018-07-12T02:51:34Z-
dc.date.issued2008-03-01en_US
dc.identifier.citationMolecular Pharmacology. Vol.73, No.3 (2008), 801-812en_US
dc.identifier.issn15210111en_US
dc.identifier.issn0026895Xen_US
dc.identifier.other2-s2.0-40849083785en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40849083785&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/19879-
dc.description.abstractExcess formation of nitric oxide and superoxide by-products (peroxynitrite, reactive oxygen, and reactive nitrogen species) attenuates cholinergic transmission potentially having a role in Alzheimer disease pathogenesis. In this study, we investigated mechanisms by which acute exposure to peroxynitrite impairs function of the sodium-dependent hemicholinium-3 (HC-3)-sensitive choline transporter (CHT) that provides substrate for acetylcholine synthesis. The peroxynitrite generator 3-morpholinosydnonimine (SIN-1) acutely inhibited choline uptake in cells stably expressing FLAG-tagged rat CHT in a dose- and time-dependent manner, with an IC50 = 0.9 ± 0.14 mM and t 1/2 = 4 min. SIN-1 significantly reduced Vmax of choline uptake without altering the Km. This correlated with a SIN-1-induced decrease in cell surface CHT protein, observed as lowered levels of HC-3 binding and biotinylated CHT at the plasma membrane. It is noteworthy that short-term exposure of cells to SIN-1 accelerated the rate of internalization of CHT from the plasma membrane, but it did not alter return of CHT back to the cell surface. SIN-1 did not disrupt cell membrane integrity or cause cell death. Thus, the inhibitory effect of SIN-1 on choline uptake activity and HC-3 binding was related to enhanced internalization of CHT proteins from the plasma membrane to subcellular organelles. Copyright © 2008 The American Society for Pharmacology and Experimental Therapeutics.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40849083785&origin=inwarden_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleActivity and subcellular trafficking of the sodium-coupled choline transporter CHT is regulated acutely by peroxynitriteen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1124/mol.107.040881en_US
Appears in Collections:Scopus 2006-2010

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