Evidence map›Paper›PMID 35934753›Full record

ArticleBrain structure & function2022

Origin of thyrotropin-releasing hormone neurons that innervate the tuberomammillary nuclei.

Edith Sánchez-Jaramillo, Gábor Wittmann, Judit Menyhért, Praful Singru, Gabriela B Gómez-González, Eduardo Sánchez-Islas, Nashiely Yáñez-Recendis, Jaime Arturo Pimentel-Cabrera, Martha León-Olea, Balázs Gereben and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 4 countries.

Edith Sánchez-Jaramillo *Laboratorio de Neuroendocrinología Molecular, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, 14370, México, CDMX, México. esanchez@imp.edu.mx.ORCID http://orcid.org/0000-0002-5560-2645
Gábor Wittmann *Tupper Research Institute and Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Tufts Medical Center, Boston, MA, 02111, USA.
Judit MenyhértDepartment of Endocrine Neurobiology, Institute of Experimental Medicine, Budapest, 1083, Hungary.
Praful SingruTupper Research Institute and Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Tufts Medical Center, Boston, MA, 02111, USA.
Gabriela B Gómez-GonzálezLaboratorio de Neuroendocrinología Molecular, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, 14370, México, CDMX, México.
Eduardo Sánchez-IslasDepartamento de Neuromorfología Funcional, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, 14370, México, CDMX, México.
Nashiely Yáñez-RecendisLaboratorio de Neuroendocrinología Molecular, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, 14370, México, CDMX, México.
Jaime Arturo Pimentel-CabreraLaboratorio Nacional de Microscopia Avanzada, Instituto de Biotecnología, Universidad Nacional Autónoma de México (UNAM), 62210, Cuernavaca, MOR, México.
Martha León-OleaDepartamento de Neuromorfología Funcional, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, 14370, México, CDMX, México.
Balázs GerebenDepartment of Endocrine Neurobiology, Institute of Experimental Medicine, Budapest, 1083, Hungary.
Csaba FeketeTupper Research Institute and Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Tufts Medical Center, Boston, MA, 02111, USA.
Jean-Louis CharliDepartamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México (UNAM), 62210, Cuernavaca, MOR, México.
Ronald M LechanTupper Research Institute and Department of Medicine, Division of Endocrinology, Diabetes, and Metabolism, Tufts Medical Center, Boston, MA, 02111, USA.
Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz · MXTufts Medical Center · USHUN-REN Institute of Experimental Medicine · HUUniversidad Nacional Autónoma de México · MXTufts University · US

Funding

Anatomical and Functional Analysis of POMC Neuronal Rescue by TanycytesR21AG050663 · NIA · TUFTS MEDICAL CENTER · PI LECHAN, RONALD MICHAEL · 2015 to 2015
$206k
Consejo Nacional de Ciencia y Tecnología 265087DGAPA-UNAM PAPITT IN208515DGAPA-UNAM PAPITT IN209018INPRFM NC143290.0INPRFM NC19110.0NIA NIH HHS R21 AG050663NIH HHS AG050663
6 · The paper itself

Abstract

Hypophysiotropic thyrotropin-releasing hormone (TRH) neurons function as metabolic sensors that regulate the thyroid axis and energy homeostasis. Less is known about the role of other hypothalamic TRH neurons. As central administration of TRH decreases food intake and increases histamine in the tuberomammillary nuclei (TMN), and TMN histamine neurons are densely innervated by TRH fibers from an unknown origin, we mapped the location of TRH neurons that project to the TMN. The retrograde tracer, cholera toxin B subunit (CTB), was injected into the TMN E1-E2, E4-E5 subdivisions of adult Sprague-Dawley male rats. TMN projecting neurons were observed in the septum, preoptic area, bed nucleus of the stria terminalis (BNST), perifornical area, anterior paraventricular nucleus, peduncular and tuberal lateral hypothalamus (TuLH), suprachiasmatic nucleus and medial amygdala. However, CTB/pro-TRH178-199 double-labeled cells were only found in the TuLH. The specificity of the retrograde tract-tracing result was confirmed by administering the anterograde tracer, Phaseolus vulgaris leuco-agglutinin (PHAL) into the TuLH. Double-labeled PHAL-pro-TRH boutons were identified in all subdivisions of the TMN. TMN neurons double-labeled for histidine decarboxylase (Hdc)/PHAL, Hdc/Trh receptor (Trhr), and Hdc/Trh. Further confirmation of a TuLH-TRH neuronal projection to the TMN was established in a transgenic mouse that expresses Cre recombinase in TRH-producing cells following microinjection of a Cre recombinase-dependent AAV that expresses mCherry into the TuLH. We conclude that, in rodents, the TRH innervation of TMN originates in part from TRH neurons in the TuLH, and that this TRH population may contribute to regulate energy homeostasis through histamine Trhr-positive neurons of the TMN.

Indexed as

Hypothalamic Area, LateralThyrotropin-Releasing HormoneAnimalsHistamineMaleMiceNeuronsRatsRats, Sprague-DawleyHistamineThyrotropin-Releasing HormoneAnterogradeHistamineLateral hypothalamusRetrogradeTRHTrh–Cre transgene

Identifiers

PMID35934753
PMCPMC9418084
OpenAlexW4290422767

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.