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dc.creatorDopeso-Reyes, I.G. (Iria G.)-
dc.creatorRico, A.J. (Alberto J.)-
dc.creatorRoda, E. (Elvira)-
dc.creatorSierra, S. (Salvador)-
dc.creatorPignataro, D. (Diego)-
dc.creatorLanz, M. (María)-
dc.creatorSucunza, D. (Diego)-
dc.creatorChang-Azancot, L. (Luis)-
dc.creatorLanciego, J.L. (José Luis)-
dc.date.accessioned2015-05-18T08:29:24Z-
dc.date.available2015-05-18T08:29:24Z-
dc.date.issued2014-
dc.identifier.citationDopeso-Reyes I.G, Rico A.J, Roda E, Sierra S, Pignataro D, Lanz M, et al. Calbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaques. Front Neuroanat. 2014 Dec;8:146.es_ES
dc.identifier.issn1662-5129-
dc.identifier.urihttps://hdl.handle.net/10171/38340-
dc.description.abstractCalbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have also been suggested, particularly those related to the dopamine transporter. Indeed, several studies have reported that CB levels are not causally related to the differential vulnerability of dopaminergic neurons against neurotoxins. Here we have used dual stains for tyrosine hydroxylase (TH) and CB in 3 control and 3 MPTP-treated monkeys to visualize dopaminergic neurons in the ventral tegmental area (VTA) and in the dorsal and ventral tiers of the substantia nigra pars compacta (SNcd and SNcv) co-expressing TH and CB. In control animals, the highest percentages of co-localization were found in VTA (58.2%), followed by neurons located in the SNcd (34.7%). As expected, SNcv neurons lacked CB expression. In MPTP-treated animals, the percentage of CB-ir/TH-ir neurons in the VTA was similar to control monkeys (62.1%), whereas most of the few surviving neurons in the SNcd were CB-ir/TH-ir (88.6%). Next, we have elucidated the presence of CB within identified nigrostriatal and nigroextrastriatal midbrain dopaminergic projection neurons. For this purpose, two control monkeys received one injection of Fluoro-Gold into the caudate nucleus and one injection of cholera toxin (CTB) into the postcommissural putamen, whereas two more monkeys were injected with CTB into the internal division of the globus pallidus (GPi). As expected, all the nigrocaudate- and nigroputamen-projecting neurons were TH-ir, although surprisingly, all of these nigrostriatal-projecting neurons were negative for CB. Furthermore, all the nigropallidal-projecting neurons co-expressed both TH and CB. In summary, although CB-ir dopaminergic neurons seem to be less prone to MPTPinduced degeneration, our data clearly demonstrated that these neurons are not giving rise to nigrostriatal projections and indeed CB-ir/TH-ir neurons only originate nigroextrastriatal projections.es_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectCalbindines_ES
dc.subjectParkinson’s diseasees_ES
dc.subjectNigroextrastriatal pathwayes_ES
dc.subjectNeuronal tracerses_ES
dc.subjectNeuroprotectiones_ES
dc.subjectMPTPes_ES
dc.titleCalbindin content and differential vulnerability of midbrain efferent dopaminergic neurons in macaqueses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.3389/fnana.2014.00146es_ES

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