Mostrar el registro sencillo del ítem

dc.contributor.authorAlbert Gasco, Hector
dc.contributor.authorMa, Sherie
dc.contributor.authorRos Bernal, Francisco
dc.contributor.authorSánchez-Pérez, Ana María
dc.contributor.authorGundlach, Andrew Lawrence
dc.contributor.authorOlucha-Bordonau, Francisco E
dc.date.accessioned2018-03-13T11:00:14Z
dc.date.available2018-03-13T11:00:14Z
dc.date.issued2018-01-17
dc.identifier.citationALBERT GASCÓ, Héctor; MA, Sherie; ROS BERNAL, Francisco; SÁNCHEZ-PÉREZ, Ana María; GUNDLACH, Andrew L.; OLUCHA BORDONAU, Francisco E. GABAergic Neurons in the Rat Medial Septal Complex Express Relaxin-3 Receptor (RXFP3) mRNA. Frontiers in Neuroanatomy (2018), v. 11ca_CA
dc.identifier.urihttp://hdl.handle.net/10234/173328
dc.description.abstractThe medial septum (MS) complex modulates hippocampal function and related behaviors. Septohippocampal projections promote and control different forms of hippocampal synchronization. Specifically, GABAergic and cholinergic projections targeting the hippocampal formation from the MS provide bursting discharges to promote theta rhythm, or tonic activity to promote gamma oscillations. In turn, the MS is targeted by ascending projections from the hypothalamus and brainstem. One of these projections arises from the nucleus incertus in the pontine tegmentum, which contains GABA neurons that co-express the neuropeptide relaxin-3 (Rln3). Both stimulation of the nucleus incertus and septal infusion of Rln3 receptor agonist peptides promotes hippocampal theta rhythm. The Gi=o-protein-coupled receptor, relaxin-family peptide receptor 3 (RXFP3), is the cognate receptor for Rln3 and identification of the transmitter phenotype of neurons expressing RXFP3 in the septohippocampal system can provide further insights into the role of Rln3 transmission in the promotion of septohippocampal theta rhythm. Therefore, we used RNAscope multiplex in situ hybridization to characterize the septal neurons expressing Rxfp3 mRNA in the rat. Our results demonstrate that Rxfp3 mRNA is abundantly expressed in vesicular GABA transporter (vGAT) mRNA- and parvalbumin (PV) mRNA-positive GABA neurons in MS, whereas ChAT mRNA-positive acetylcholine neurons lack Rxfp3 mRNA. Approximately 75% of Rxfp3 mRNA-positive neurons expressed vGAT mRNA (and 22% were PV mRNA-positive), while the remaining 25% expressed Rxfp3 mRNA only, consistent with a potential glutamatergic phenotype. Similar proportions were observed in the posterior septum. The occurrence of RXFP3 in PV-positive GABAergic neurons gives support to a role for the Rln3-RXFP3 system in septohippocampal theta rhythm.ca_CA
dc.format.extent16 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherFrontiers Mediaca_CA
dc.relation.isPartOfFrontiers in Plant Science (2018), v. 11ca_CA
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-sa/4.0/*
dc.subjectArousalca_CA
dc.subjectChATca_CA
dc.subjectEmotionca_CA
dc.subjectGABAca_CA
dc.subjectHippocampusca_CA
dc.subjectNucleus incertusca_CA
dc.subjectRelaxin-3ca_CA
dc.subjectTheta rhythmca_CA
dc.titleGABAergic Neurons in the Rat Medial Septal Complex Express Relaxin-3 Receptor (RXFP3) mRNAca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.3389/fnana.2017.00133
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_CA
dc.relation.publisherVersionhttps://www.frontiersin.org/articles/10.3389/fnana.2017.00133/fullca_CA
dc.contributor.funder1) Universitat Jaume I FPI-UJI Predoctoral Research Scholarship PREDOC/2014/35 (HA-G); 2) E-2016-43 Research Travel Grant (HA-G); 3) NHMRC (Australia) Project Grant 1067522 (ALG); 4) Dorothy Levien Foundation Research Grant (ALG); and 5) Universitat Jaume I Research Grant UJI-B2016-40 (FEO-B).ca_CA
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA


Ficheros en el ítem

Thumbnail
Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem

Atribución 4.0 Internacional
Excepto si se señala otra cosa, la licencia del ítem se describe como: Atribución 4.0 Internacional