Evidence map›Paper›PMID 26974501›Full record

ArticlePsychoneuroendocrinology2016

Sympathetic nervous system contributes to enhanced corticosterone levels following chronic stress.

Steven A Lowrance, Amy Ionadi, Erin McKay, Xavier Douglas, John D Johnson

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

49 citing papers in PubMed, 94 citations in OpenAlex.

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  16. The Human Superficial Fascia: A Narrative Review.International journal of molecular sciences · 2025
    Review
  17. Noradrenaline Regulation of Brain-Body Communication.Advances in experimental medicine and biology · 2025
    Review
  18. Disentangling the Neural Circuits of Arousal and Anxiety-Like Behavior.Current topics in behavioral neurosciences · 2025
    Review
  19. Review
  20. Article
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

5 authors at 1 institution in 1 country.

Steven A LowranceDepartment of Biological Sciences, Kent State University, Kent, OH 44242 USA.
Amy IonadiDepartment of Biological Sciences, Kent State University, Kent, OH 44242 USA; School of Biomedical Sciences, Kent State University, Kent, OH 44242 USA.
Erin McKayDepartment of Biological Sciences, Kent State University, Kent, OH 44242 USA.
Xavier DouglasDepartment of Biological Sciences, Kent State University, Kent, OH 44242 USA.
John D JohnsonDepartment of Biological Sciences, Kent State University, Kent, OH 44242 USA; School of Biomedical Sciences, Kent State University, Kent, OH 44242 USA. Electronic address: jjohns72@kent.edu.
Kent State University · US

Funding

Stress-Induced Noradrenergic Dysregulation of Neuroinflammation & HPA ResponsesR15MH099580 · NIMH · KENT STATE UNIVERSITY · PI JOHNSON, JOHN D · 2013 to 2013
$442k
NIMH NIH HHS R15 MH099580
6 · The paper itself

Abstract

Exposure to chronic stress often elevates basal circulating glucocorticoids during the circadian nadir and leads to exaggerated glucocorticoid production following exposure to subsequent stressors. While glucocorticoid production is primarily mediated by the hypothalamic-pituitary-adrenal (HPA) axis, there is evidence that the sympathetic nervous system can affect diurnal glucocorticoid production by direct actions at the adrenal gland. Experiments here were designed to examine the role of the HPA and sympathetic nervous system in enhancing corticosterone production following chronic stress. Rats were exposed to a four-day stress paradigm or control conditions then exposed to acute restraint stress on the fifth day to examine corticosterone and ACTH responses. Repeated stressor exposure resulted in a small increase in corticosterone, but not ACTH, during the circadian nadir, and also resulted in exaggerated corticosterone production 5, 10, and 20min following restraint stress. While circulating ACTH levels increased after 5min of restraint, levels were not greater in chronic stress animals compared to controls until following 20min. Administration of astressin (a CRH antagonist) prior to restraint stress significantly reduced ACTH responses but did not prevent the sensitized corticosterone response in chronic stress animals. In contrast, administration of chlorisondamine (a ganglionic blocker) returned basal corticosterone levels in chronic stress animals to normal levels and reduced early corticosterone production following restraint (up to 10min) but did not block the exaggerated corticosterone response in chronic stress animals at 20min. These data indicate that increased sympathetic nervous system tone contributes to elevated basal and rapid glucocorticoid production following chronic stress, but HPA responses likely mediate peak corticosterone responses to stressors of longer duration.

Indexed as

Adrenal GlandsAdrenocorticotropic HormoneAnimalsCircadian RhythmCorticosteroneGlucocorticoidsHypothalamo-Hypophyseal SystemMalePituitary-Adrenal SystemRatsRats, Inbred F344Receptors, GlucocorticoidStress, PhysiologicalStress, PsychologicalSympathetic Nervous SystemAdrenocorticotropic HormoneCorticosteroneGlucocorticoidsReceptors, GlucocorticoidACTHCorticosteroneCRHGanglionic blockerHPA axis

Identifiers

PMID26974501
PMCPMC5656452
OpenAlexW2285947238

What OpenQuestion holds

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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.