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Control óptico de ensambles neuronales patológicos en un modelo de la enfermedad de parkinson

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dc.contributor NADIA SADERI;257613 es_MX
dc.contributor.advisor Saderi, Nadia es_MX
dc.contributor.advisor Carrillo Reid, Luis es_MX
dc.contributor.advisor Castillo Martin del Campo, Claudia es_MX
dc.contributor.advisor Salgado Delgado, Roberto Carlos es_MX
dc.contributor.advisor Ibáñez Sandoval, Osvaldo es_MX
dc.contributor.advisor Téllez Lima, Luis es_MX
dc.contributor.author Zamora Ursulo, Miguel Ángel es_MX
dc.coverage.spatial México. San Luis Potosí. San Luis Potosí es_MX
dc.creator MIGUEL ANGEL ZAMORA URSULO;770504 es_MX
dc.date.accessioned 2024-03-05T17:30:02Z
dc.date.available 2024-03-05T17:30:02Z
dc.date.issued 2024-02
dc.identifier.uri https://repositorioinstitucional.uaslp.mx/xmlui/handle/i/8563
dc.identifier.uri https://doi.org/10.1371/journal.pone.0290317 es_MX
dc.description.abstract Motor deficits observed in Parkinson’s disease (PD) are caused by the loss of dopaminergic neurons and the subsequent dopamine depletion in different brain areas. The most common therapy to treat motor symptoms for patients with this disorder is the systemic intake of L- DOPA that increases dopamine levels in all the brain, making it difficult to discern the main locus of dopaminergic action in the alleviation of motor control. Caged compounds are molecules with the ability to release neuromodulators locally in temporary controlled conditions using light. In the present study, we measured the turning behavior of unilateral dopamine depleted mice before and after dopamine uncaging. The optical delivery of dopamine in the striatum of lesioned mice produced contralateral turning behavior that resembled, to a lesser extent, the contralateral turning behavior evoked by a systemic injection of apomorphine. Contralateral turning behavior induced by dopamine uncaging was temporarily tied to the transient elevation of dopamine concentration and was reversed when dopamine decreased to pathological levels. Remarkably, contralateral turning behavior was tuned by changing the power and frequency of light stimulation, opening the possibility to modulate dopamine fluctuations using different light stimulation protocols. Moreover, striatal dopamine uncaging recapitulated the motor effects of a low concentration of systemic L-DOPA, but with better temporal control of dopamine levels. Finally, dopamine uncaging reduced the pathological synchronization of striatal neuronal ensembles that characterize unilateral dopamine- depleted mice. We conclude that optical delivery of dopamine in the striatum resembles the motor effects induced by systemic injection of dopaminergic agonists in unilateral dopamine-depleted mice. Future experiments using this approach could help to elucidate the role of dopamine in different brain nuclei in normal and pathological conditions. es_MX
dc.description.statementofresponsibility Investigadores es_MX
dc.description.statementofresponsibility Estudiantes es_MX
dc.language Inglés es_MX
dc.publisher Facultad de Medicina es_MX
dc.relation.ispartof REPOSITORIO NACIONAL CONACYT es_MX
dc.rights Acceso Abierto es_MX
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0 es_MX
dc.subject Parkinson´s disease es_MX
dc.subject Caged compound es_MX
dc.subject Movement disorders es_MX
dc.subject Dopamine es_MX
dc.subject optical stimulation es_MX
dc.subject Enfermedad de parkinson (bvs) es_MX
dc.subject Dopamina (bvs) es_MX
dc.subject.other MEDICINA Y CIENCIAS DE LA SALUD es_MX
dc.title Control óptico de ensambles neuronales patológicos en un modelo de la enfermedad de parkinson es_MX
dc.title.alternative Reversal of pathological motor behavior in a model of Parkinson’s disease by striatal dopamine uncaging es_MX
dc.type Tesis de doctorado es_MX
dc.degree.name Doctorado en Ciencias Biomédicas Básicas es_MX
dc.degree.department Facultad de Medicina es_MX


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