Evidence map›Paper›PMID 28351560›Full record

ArticlePhysiology & behavior2017

Chronic salt-loading reduces basal excitatory input to CRH neurons in the paraventricular nucleus and accelerates recovery from restraint stress in male mice.

Eric G Krause, Dipanwita Pati, Charles J Frazier

Abstract read
In one paragraph

Article in Physiology & behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Vasopressin and v1br gene expression is increased in the hypothalamic pvn of borderline hypertensive rats.Hypertension research : official journal of the Japanese Society of Hypertension · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. The Neurocircuitry of fluid satiation.Physiological reports · 2018
    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

3 authors at 1 institution in 1 country.

Eric G KrauseDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, United States.
Dipanwita PatiDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, United States.
Charles J FrazierDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, United States; Department of Neuroscience, College of Medicine, University of Florida, United States. Electronic address: cjfraz@ufl.edu.
University of Florida · US

Funding

Central Mechanisms Underlying the Stress Dampening Effects of Acute HypernatremiaR01HL122494 · NHLBI · UNIVERSITY OF FLORIDA · PI KRAUSE, ERIC GERALD · 2015 to 2019
$1.9M
Novel Aspects of Central Oxytocin Signaling Relevant to Mood/Anxiety DisordersR01MH104641 · NIMH · UNIVERSITY OF FLORIDA · PI FRAZIER, CHARLES J · 2015 to 2019
$1.9M
NHLBI NIH HHS R01 HL122494NIMH NIH HHS R01 MH104641
6 · The paper itself

Abstract

Neurons synthesizing corticotrophin-releasing hormone (CRH) in the paraventricular nucleus of the hypothalamus (PVN) are activated during acute stress and act via the hypothalamic-pituitary-adrenal (HPA) axis to increase systemic levels of corticosterone (CORT). Recent data indicates that CRH neurons in the PVN are inhibited by acute salt-loading, and that this inhibition blunts the response to restraint stress as measured by increases in plasma CORT. The current study evaluates the effects of chronic rather than acute salt-loading on stress-induced activation of the HPA axis. Relative to euhydrated controls, chronic salt-loading over a 5-day period elevated plasma sodium and fluid intake without eliciting hypovolemia or substantial alterations in food intake or body weight. Chronic salt-loading also decreased expression of CRH mRNA in the anterior but not posterior portion of the PVN. Similarly, whole cell patch clamp recordings revealed that salt-loading effectively decreases spontaneous excitatory input to CRH neurons in the PVN without altering spontaneous inhibitory input. Generally consistent with these observations, chronic salt attenuated HPA axis activation as indicated by a significant reduction of plasma CORT during recovery from restraint stress.

Indexed as

AnimalsArea Under CurveCorticotropin-Releasing HormoneDrinkingElectric StimulationExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsLuminescent ProteinsMaleMiceMice, TransgenicMutationNeuronsParaventricular Hypothalamic NucleusPatch-Clamp TechniquesQuinoxalines2-amino-5-phosphopentanoic acidCorticotropin-Releasing HormoneExcitatory Amino Acid AntagonistsFG 9041Luminescent ProteinsQuinoxalinesRNA, MessengerSaltsSodiumValine

Identifiers

PMID28351560
PMCPMC5632528
OpenAlexW2599038246

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.