Evidence map›Paper›PMID 30758330›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

β1-adrenergic receptors mediate plasma acyl-ghrelin elevation and depressive-like behavior induced by chronic psychosocial stress.

Deepali Gupta, Jen-Chieh Chuang, Bharath K Mani, Kripa Shankar, Juan A Rodriguez, Sherri Osborne-Lawrence, Nathan P Metzger, Jeffrey M Zigman

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. An Emerging Role for Gut-Brain Signaling Involving Ghrelin in Chronic Stress.Advances in experimental medicine and biology · 2025
    Review
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  11. Ghrelin receptor signaling in health and disease: a biased view.Trends in endocrinology and metabolism: TEM · 2023
    Review
  12. Article
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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

8 authors at 2 institutions in 1 country.

Deepali GuptaDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Jen-Chieh ChuangDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Bharath K ManiDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Kripa ShankarDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Juan A RodriguezDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.ORCID http://orcid.org/0000-0002-5236-5015
Sherri Osborne-LawrenceDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Nathan P MetzgerDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA.
Jeffrey M ZigmanDepartment of Internal Medicine, Division of Hypothalamic Research, UT Southwestern Medical Center, 5323 Harry Hines Blvd., MC9077, Dallas, TX, 75390-9077, USA. jeffrey.zigman@utsouthwestern.edu.
Southwestern Medical CenterSouthwestern Medical Center · US

Funding

Role of the hormone LEAP2 in eating, body weight, blood glucose and survivalR01DK103884 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ZIGMAN, JEFFREY M · 2015 to 2023
$3.4M
NIDDK NIH HHS R01 DK103884
6 · The paper itself

Abstract

The ghrelin system is a key component of the mood and metabolic responses to chronic psychosocial stress. For example, circulating acyl-ghrelin rises in several rodent and human stress models, administered acyl-ghrelin induces antidepressant-like behavioral responses in mice, and mice with deleted ghrelin receptors (GHSRs) exhibit exaggerated depressive-like behaviors, changed eating behaviors, and altered metabolism in response to chronic stress. However, the mechanisms mediating stress-induced rises in ghrelin are unknown and ghrelin's antidepressant-like efficacy in the setting of chronic stress is incompletely characterized. Here, we used a pharmacological approach in combination with a 10-day chronic social defeat stress (CSDS) model in male mice to investigate whether the sympathoadrenal system is involved in the ghrelin response to stress. We also examined the antidepressant-like efficacy of administered ghrelin and the synthetic GHSR agonist GHRP-2 during and/or after CSDS. We found that administration of the β1-adrenergic receptor (β1AR) blocker atenolol during CSDS blunts the elevation of plasma acyl-ghrelin and exaggerates depressive-like behavior. Neither acute injection of acyl-ghrelin directly following CSDS nor its chronic administration during or after CSDS nor chronic delivery of GHRP-2 during and after CSDS improved stress-induced depressive-like behavior. Thus, β1ARs drive the acyl-ghrelin response to CSDS, but supplementing the natural increases in acyl-ghrelin with exogenous acyl-ghrelin or GHSR agonist does not further enhance the antidepressant-like actions of the endogenous ghrelin system in the setting of CSDS.

Indexed as

Adrenergic beta-1 Receptor AntagonistsAnimalsAtenololDepressionGhrelinMaleMiceMice, Inbred C57BLOligopeptidesReceptors, Adrenergic, beta-1Social BehaviorStress, PsychologicalAdrenergic beta-1 Receptor AntagonistsAtenololGhrelingrowth hormone-releasing peptide-2OligopeptidesReceptors, Adrenergic, beta-1

Identifiers

PMID30758330
PMCPMC6785135
OpenAlexW2914153312

What OpenQuestion holds

Textmetadata
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.