Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/445
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dc.contributor.authorAngelovski, Goranen_US
dc.contributor.authorGottschalk, Svenen_US
dc.contributor.authorMilošević, Milenaen_US
dc.contributor.authorEngelmann, Jörnen_US
dc.contributor.authorHagberg, Gisela E.en_US
dc.contributor.authorKadjane, Pascalen_US
dc.contributor.authorAnđus, Pavleen_US
dc.contributor.authorLogothetis, Nikos K.en_US
dc.date.accessioned2019-07-03T12:04:57Z-
dc.date.available2019-07-03T12:04:57Z-
dc.date.issued2014-05-21-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/445-
dc.description.abstractResponsive or smart contrast agents (SCAs) represent a promising direction for development of novel functional MRI (fMRI) methods for the eventual noninvasive assessment of brain function. In particular, SCAs that respond to Ca2+ may allow tracking neuronal activity independent of brain vasculature, thus avoiding the characteristic limitations of current fMRI techniques. Here we report an in vitro proof-of-principle study with a Ca 2+-sensitive, Gd3+-based SCA in an attempt to validate its potential use as a functional in vivo marker. First, we quantified its relaxometric response in a complex 3D cell culture model. Subsequently, we examined potential changes in the functionality of primary glial cells following administration of this SCA. Monitoring intracellular Ca2+ showed that, despite a reduction in the Ca2+ level, transport of Ca 2+ through the plasma membrane remained unaffected, while stimulation with ATP induced Ca2+-transients suggested normal cellular signaling in the presence of low millimolar SCA concentrations. SCAs merely lowered the intracellular Ca2+ level. Finally, we estimated the longitudinal relaxation times (T1) for an idealized in vivo fMRI experiment with SCA, for extracellular Ca2+ concentration level changes expected during intense neuronal activity which takes place upon repetitive stimulation. The values we obtained indicate changes in T1 of around 1-6%, sufficient to be robustly detectable using modern MRI methods in high field scanners. Our results encourage further attempts to develop even more potent SCAs and appropriate fMRI protocols. This would result in novel methods that allow monitoring of essential physiological processes at the cellular and molecular level. © 2014 American Chemical Society.en_US
dc.language.isoenen_US
dc.relation.ispartofACS Chemical Neuroscienceen_US
dc.subjectCalciumen_US
dc.subjectfunctional magnetic resonance imagingen_US
dc.subjectresponsive/smart contrast agentsen_US
dc.titleInvestigation of a calcium-responsive contrast agent in cellular model systems: Feasibility for use as a smart molecular probe in functional mrien_US
dc.typeArticleen_US
dc.identifier.doi10.1021/cn500049n-
dc.identifier.pmid24712900-
dc.identifier.scopus2-s2.0-84901271804-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84901271804-
item.cerifentitytypePublications-
item.grantfulltextrestricted-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0002-6138-6766-
crisitem.author.orcid0000-0002-8468-8513-
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