Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/675
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dc.contributor.authorAnđus, Pavleen_US
dc.contributor.authorKhiroug, Leonarden_US
dc.contributor.authorNistri, Andreaen_US
dc.contributor.authorCherubini, Enricoen_US
dc.date.accessioned2019-07-05T13:06:10Z-
dc.date.available2019-07-05T13:06:10Z-
dc.date.issued1996-01-01-
dc.identifier.issn0959-4965-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/675-
dc.description.abstractConfocal laser scanning microscopy (with the fluorescent calcium dye fluo-3) was used to test the effect of IgG obtained from patients with amyotrophic lateral sclerosis (ALS) on the KCl-induced [Ca2+](i) rise in rat hippocampal neurones in culture. In the presence of tetrodotoxin and ionotropic glutamate receptor antagonists, ALS IgGs depressed (by 30-40%) Ca2+ transients evoked by influx of Ca2+ through voltage-activated channels; such an effect did not occur with IgG obtained from healthy donors. The depressant action of ALS IgG was selectively prevented by the inhibitor of P/Q-type Ca2+ channels, ω-agatoxin IVA (which alone reduced Ca2+ transients by 40%). The reduced Ca2+ transients might impair Ca2+-dependent glutamate receptor desensitization and thus facilitate excitotoxic damage.en_US
dc.language.isoenen_US
dc.relation.ispartofNeuroReporten_US
dc.subjectALSen_US
dc.subjectcalcium channelsen_US
dc.subjectconfocal microscopyen_US
dc.subjectcultureen_US
dc.subjecthippocampal neuronesen_US
dc.subjectintracellular calciumen_US
dc.titleALS IgGs suppress [Ca<sup>2+</sup>](i) rise through P/Q-type calcium channels in central neurones in cultureen_US
dc.typeArticleen_US
dc.identifier.doi10.1097/00001756-199608120-00008-
dc.identifier.pmid8905691-
dc.identifier.scopus2-s2.0-0029997131-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0029997131-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.grantfulltextrestricted-
item.languageiso639-1en-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0002-8468-8513-
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