Evidence map›Paper›PMID 32200401›Full record

ArticleBrain structure & function2020

Colocalized neurotransmitters in the hindbrain cooperate in adaptation to chronic hypernatremia.

Rita Matuska, Dóra Zelena, Katalin Könczöl, Rege Sugárka Papp, Máté Durst, Dorina Guba, Bibiana Török, Peter Varnai, Zsuzsanna E Tóth

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2020. 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
0.1field-weighted citation impact, top 62% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
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

9 authors at 2 institutions in 1 country.

Rita MatuskaDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Dóra ZelenaBehavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Katalin KönczölDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
Rege Sugárka PappHuman Brain Tissue Bank and Microdissection Laboratory, Semmelweis University, Budapest, Hungary.
Máté DurstDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
Dorina GubaDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary.
Bibiana TörökBehavioral Neurobiology, Institute of Experimental Medicine, Budapest, Hungary.
Peter VarnaiDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Zsuzsanna E TóthDepartment of Anatomy, Histology and Embryology, Semmelweis University, Budapest, Hungary. toth.zsuzsanna.emese@med.semmelweis-univ.hu.ORCID http://orcid.org/0000-0002-0628-1320
Semmelweis University · HUHUN-REN Institute of Experimental Medicine · HU

Funding

Hungarian Scientific Research Fund 120311Nemzeti Kutatási, Fejlesztési és Innovációs Hivatal 115422
6 · The paper itself

Abstract

Chronic hypernatremia activates the central osmoregulatory mechanisms and inhibits the function of the hypothalamic-pituitary-adrenal (HPA) axis. Noradrenaline (NE) release into the periventricular anteroventral third ventricle region (AV3V), the supraoptic (SON) and hypothalamic paraventricular nuclei (PVN) from efferents of the caudal ventrolateral (cVLM) and dorsomedial (cDMM) medulla has been shown to be essential for the hypernatremia-evoked responses and for the HPA response to acute restraint. Notably, the medullary NE cell groups highly coexpress prolactin-releasing peptide (PrRP) and nesfatin-1/NUCB2 (nesfatin), therefore, we assumed they contributed to the reactions to chronic hypernatremia. To investigate this, we compared two models: homozygous Brattleboro rats with hereditary diabetes insipidus (DI) and Wistar rats subjected to chronic high salt solution (HS) intake. HS rats had higher plasma osmolality than DI rats. PrRP and nesfatin mRNA levels were higher in both models, in both medullary regions compared to controls. Elevated basal tyrosine hydroxylase (TH) expression and impaired restraint-induced TH, PrRP and nesfatin expression elevations in the cVLM were, however, detected only in HS, but not in DI rats. Simultaneously, only HS rats exhibited classical signs of chronic stress and severely blunted hormonal reactions to acute restraint. Data suggest that HPA axis responsiveness to restraint depends on the type of hypernatremia, and on NE capacity in the cVLM. Additionally, NE and PrRP signalization primarily of medullary origin is increased in the SON, PVN and AV3V in HS rats. This suggests a cooperative action in the adaptation responses and designates the AV3V as a new site for PrRP's action in hypernatremia.

Indexed as

Adaptation, PhysiologicalAnimalsHypernatremiaHypothalamusMaleMedulla OblongataNucleobindinsProlactin-Releasing HormoneRats, BrattleboroRats, WistarStress, PsychologicalTyrosine 3-MonooxygenaseNucb2 protein, ratNucleobindinsProlactin-Releasing HormoneTyrosine 3-MonooxygenaseBrattleboro ratNesfatin-1NoradrenalineProlactin-releasing peptideRestraintStress

Identifiers

PMID32200401
PMCPMC7166202
OpenAlexW3012872666

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.