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dc.contributor.authorEscobedo-Ávila, Itzel-
dc.contributor.authorVargas-Romero, Fernanda-
dc.contributor.authorMolina-Hernández, Anayansi-
dc.contributor.authorLópez-González, Rodrigo-
dc.contributor.authorCortés, Daniel-
dc.contributor.authorCarlos, Juan A. de-
dc.contributor.authorVelasco, Iván-
dc.date.accessioned2015-11-25T17:55:04Z-
dc.date.available2015-11-25T17:55:04Z-
dc.date.issued2014-08-12-
dc.identifier.citationMolecular Brain 7(1): 58 (2014)-
dc.identifier.issn1756-6606-
dc.identifier.urihttp://hdl.handle.net/10261/125868-
dc.description.abstract[Background] Histamine (HA) regulates the sleep-wake cycle, synaptic plasticity and memory in adult mammals. Dopaminergic specification in the embryonic ventral midbrain (VM) coincides with increased HA brain levels. To study the effect of HA receptor stimulation on dopamine neuron generation, we administered HA to dopamine progenitors, both in vitro and in vivo.-
dc.description.abstract[Results] Cultured embryonic day 12 (E12) VM neural stem/progenitor cells expressed transcripts for HA receptors H1R, H2R and H3R. These undifferentiated progenitors increased intracellular calcium upon HA addition. In HA-treated cultures, dopamine neurons significantly decreased after activation of H1R. We performed intrauterine injections in the developing VM to investigate HA effects in vivo. HA administration to E12 rat embryos notably reduced VM Tyrosine Hydroxylase (TH) staining 2 days later, without affecting GABA neurons in the midbrain, or serotonin neurons in the mid-hindbrain boundary. qRT-PCR and Western blot analyses confirmed that several markers important for the generation and maintenance of dopaminergic lineage such as TH, Lmx1a and Lmx1b were significantly diminished. To identify the cell type susceptible to HA action, we injected embryos of different developmental stages, and found that neural progenitors (E10 and E12) were responsive, whereas differentiated dopaminergic neurons (E14 and E16) were not susceptible to HA actions. Proliferation was significantly diminished, whereas neuronal death was not increased in the VM after HA administration. We injected H1R or H2R antagonists to identify the receptor responsible for the detrimental effect of HA on dopaminergic lineage and found that activation of H1R was required.-
dc.description.abstract[Conclusion] These results reveal a novel action of HA affecting dopaminergic lineage during VM development.-
dc.description.sponsorshipThis work was supported by grants from Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México (Papiit IN208713), Consejo Nacional de Ciencia y Tecnología (CONACyT 131281) to I.V., and by the Ministerio de Ciencia e Innovación de España (Grant BFU2010-21377) to J.A.D.C. Itzel Escobedo-Avila, Rodrigo López-González and Daniel Cortés received a graduate fellowship from CONACyT. Fernanda Vargas-Romero received an undergraduate fellowship from DGAPA (IN208713).-
dc.publisherBioMed Central-
dc.relation.isversionofPublisher's versión-
dc.rightsopenAccess-
dc.subjectNeural stem cells-
dc.subjectMidbrain development-
dc.subjectDopaminergic neurons-
dc.subjectUltrasound injections-
dc.subjectParkinson’s disease-
dc.titleHistamine impairs midbrain dopaminergic development in vivo by activating histamine type 1 receptors-
dc.typeartículo-
dc.identifier.doi10.1186/s13041-014-0058-x-
dc.relation.publisherversionhttp://dx.doi.org/10.1186/s13041-014-0058-x-
dc.date.updated2015-11-25T17:55:04Z-
dc.language.rfc3066en-
dc.rights.holderEscobedo-Avila et al.-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0-
dc.contributor.funderUniversidad Nacional Autónoma de México-
dc.contributor.funderConsejo Nacional de Ciencia y Tecnología (México)-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100005739es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003141es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
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