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      Prosomeric Hypothalamic Distribution of Tyrosine Hydroxylase Positive Cells in Adolescent Rats

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          Abstract

          Most 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.

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          Most cited references119

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          The adolescent brain and age-related behavioral manifestations.

          L Spear (2000)
          To successfully negotiate the developmental transition between youth and adulthood, adolescents must maneuver this often stressful period while acquiring skills necessary for independence. Certain behavioral features, including age-related increases in social behavior and risk-taking/novelty-seeking, are common among adolescents of diverse mammalian species and may aid in this process. Reduced positive incentive values from stimuli may lead adolescents to pursue new appetitive reinforcers through drug use and other risk-taking behaviors, with their relative insensitivity to drugs supporting comparatively greater per occasion use. Pubertal increases in gonadal hormones are a hallmark of adolescence, although there is little evidence for a simple association of these hormones with behavioral change during adolescence. Prominent developmental transformations are seen in prefrontal cortex and limbic brain regions of adolescents across a variety of species, alterations that include an apparent shift in the balance between mesocortical and mesolimbic dopamine systems. Developmental changes in these stressor-sensitive regions, which are critical for attributing incentive salience to drugs and other stimuli, likely contribute to the unique characteristics of adolescence.
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            Dopamine neuron systems in the brain: an update.

            The basic organization of the catecholamine-containing neuronal systems and their axonal projections in the brain was initially worked out using classical histofluorescence techniques during the 1960s and 1970s. The introduction of more versatile immunohistochemical methods, along with a range of highly sensitive tract-tracing techniques, has provided a progressively more detailed picture, making the dopamine system one of the best known, and most completely mapped, neurotransmitter systems in the brain. The purpose of the present review is to summarize our current knowledge of the diversity and neurochemical features of the nine dopamine-containing neuronal cell groups in the mammalian brain, their distinctive cellular properties, and their ability to regulate their dopaminergic transmitter machinery in response to altered functional demands and aging.
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              Forebrain gene expression domains and the evolving prosomeric model.

              The prosomeric model attributes morphological meaning to gene expression patterns and other data in the forebrain. It divides this territory into the same transverse segments (prosomeres) and longitudinal zones in all vertebrates. The axis and longitudinal zones of this model are widely accepted but controversy subsists about the number of prosomeres and their nature as segments. We describe difficulties encountered in establishing continuity between prosomeric limits postulated in the hypothalamus and intra-telencephalic limits. Such difficulties throw doubt on the intersegmental nature of these limits. We sketch a simplified model, in which the secondary prosencephalon (telencephalon plus hypothalamus) is a complex protosegment not subdivided into prosomeres, which exhibits patterning singularities. By contrast, we continue to postulate that prosomeres p1-p3 (i.e. the pretectum, thalamus and prethalamus) are the caudal forebrain.
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                Author and article information

                Contributors
                Journal
                Front Neuroanat
                Front Neuroanat
                Front. Neuroanat.
                Frontiers in Neuroanatomy
                Frontiers Media S.A.
                1662-5129
                06 May 2022
                2022
                : 16
                : 868345
                Affiliations
                [1] 1Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) , Buenos Aires, Argentina
                [2] 2Facultad de Ciencias Veterinarias, Universidad Nacional de La Pampa , General Pico, Argentina
                [3] 3Department of Human Anatomy and Psychobiology, School of Medicine, University of Murcia , Murcia, Spain
                [4] 4Institute of Biomedical Research of Murcia – IMIB, Virgen de la Arrixaca University Hospital , Murcia, Spain
                [5] 5PROFITH “PROmoting FITness and Health Through Physical Activity” Research Group, Department of Physical Education and Sports, Faculty of Sport Sciences, University of Granada , Granada, Spain
                [6] 6Department of Human Anatomy and Psychobiology, Faculty of Psychology, University of Murcia , Murcia, Spain
                Author notes

                Edited by: Loreta Medina, Universitat de Lleida, Spain

                Reviewed by: Miguel Ángel García-Cabezas, Autonomous University of Madrid, Spain; Maria E. Grigoriou, Democritus University of Thrace, Greece

                *Correspondence: José Luis Ferran, jlferran@ 123456um.es

                These authors have contributed equally to this work and share first authorship

                Article
                10.3389/fnana.2022.868345
                9121318
                2fc59f2a-6850-4674-94ee-72973535c668
                Copyright © 2022 Bilbao, Garrigos, Martinez-Morga, Toval, Kutsenko, Bautista, Barreda, Ribeiro Do-Couto, Puelles and Ferran.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 02 February 2022
                : 25 February 2022
                Page count
                Figures: 15, Tables: 0, Equations: 0, References: 119, Pages: 36, Words: 22212
                Funding
                Funded by: Agencia Estatal de Investigación, doi 10.13039/501100011033;
                Funded by: Fundación Séneca, doi 10.13039/100007801;
                Categories
                Neuroanatomy
                Original Research

                Neurosciences
                pomc,hypothalamic dopamine,terminal hypothalamus,peduncular hypothalamus,acroterminal hypothalamus,arcuate nucleus,paraventricular nucleus,a13 group

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