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dc.contributor.authorBilbao, María G.
dc.contributor.authorToval Sánchez, José Ángel
dc.date.accessioned2022-06-08T06:47:31Z
dc.date.available2022-06-08T06:47:31Z
dc.date.issued2022-05-06
dc.identifier.citationBilbao MG... [et al.] (2022) Prosomeric Hypothalamic Distribution of Tyrosine Hydroxylase Positive Cells in Adolescent Rats. Front. Neuroanat. 16:868345. doi: [10.3389/fnana.2022.868345]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/75322
dc.descriptionThis study was funded by the Spanish Ministry of Science, Innovation, and Universities (MCIU), State Research Agency (AEI), and European Regional Development Fund (FEDER); PGC2018-098229-B-100 to JF and by Seneca Foundation (19904/GERM/15).es_ES
dc.description.abstractMost of the studies on neurochemical mapping, connectivity, and physiology in the hypothalamic region were carried out in rats and under the columnar morphologic paradigm. According to the columnar model, the entire hypothalamic region lies ventrally within the diencephalon, which includes preoptic, anterior, tuberal, and mamillary anteroposterior regions, and sometimes identifying dorsal, intermediate, and ventral hypothalamic partitions. This model is weak in providing little or no experimentally corroborated causal explanation of such subdivisions. In contrast, the modern prosomeric model uses different axial assumptions based on the parallel courses of the brain floor, alar-basal boundary, and brain roof (all causally explained). This model also postulates that the hypothalamus and telencephalon jointly form the secondary prosencephalon, separately from and rostral to the diencephalon proper. The hypothalamus is divided into two neuromeric (transverse) parts called peduncular and terminal hypothalamus (PHy and THy). The classic anteroposterior (AP) divisions of the columnar hypothalamus are rather seen as dorsoventral subdivisions of the hypothalamic alar and basal plates. In this study, we offered a prosomeric immunohistochemical mapping in the rat of hypothalamic cells expressing tyrosine hydroxylase (TH), which is the enzyme that catalyzes the conversion of L-tyrosine to levodopa (L-DOPA) and a precursor of dopamine. This mapping was also combined with markers for diverse hypothalamic nuclei [agouti-related peptide (Agrp), arginine vasopressin (Avp), cocaine and amphetamine-regulated transcript (Cart), corticotropin releasing Hormone (Crh), melanin concentrating hormone (Mch), neuropeptide Y (Npy), oxytocin/neurophysin I (Oxt), proopiomelanocortin (Pomc), somatostatin (Sst), tyrosine hidroxilase (Th), and thyrotropin releasing hormone (Trh)]. TH-positive cells are particularly abundant within the periventricular stratum of the paraventricular and subparaventricular alar domains. In the tuberal region, most labeled cells are found in the acroterminal arcuate nucleus and in the terminal periventricular stratum. The dorsal retrotuberal region (PHy) contains the A13 cell group of TH-positive cells. In addition, some TH cells appear in the perimamillary and retromamillary regions. The prosomeric model proved useful for determining the precise location of TH-positive cells relative to possible origins of morphogenetic signals, thus aiding potential causal explanation of position-related specification of this hypothalamic cell type.es_ES
dc.description.sponsorshipState Research Agency (AEI)es_ES
dc.description.sponsorshipEuropean Commission PGC2018-098229-B-100es_ES
dc.description.sponsorshipFundacion Seneca 19904/GERM/15es_ES
dc.description.sponsorshipSpanish Governmentes_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectPOMCes_ES
dc.subjectHypothalamic dopaminees_ES
dc.subjectTerminal hypothalamuses_ES
dc.subjectPeduncular hypothalamuses_ES
dc.subjectAcroterminal hypothalamuses_ES
dc.subjectArcuate nucleuses_ES
dc.subjectParaventricular nucleuses_ES
dc.subjectA13 groupes_ES
dc.titleProsomeric Hypothalamic Distribution of Tyrosine Hydroxylase Positive Cells in Adolescent Ratses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3389/fnana.2022.868345
dc.type.hasVersionVoRes_ES


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