Evidence map›Paper›PMID 29311652›Full record

ArticleMolecular psychiatry2019

Adult-generated neurons born during chronic social stress are uniquely adapted to respond to subsequent chronic social stress.

Zurine De Miguel, Ursula Haditsch, Theo D Palmer, Arantza Azpiroz, Robert M Sapolsky

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

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  5. Life extension factor klotho regulates behavioral responses to stress via modulation of GluN2B function in the nucleus accumbens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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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

5 authors at 2 institutions in 2 countries.

Zurine De MiguelDepartment of Biological Sciences, Stanford University, Stanford, CA, 94305, USA. zurine@stanford.edu.
Ursula HaditschInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Theo D PalmerInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Arantza AzpirozDepartment of Basic Psychological Processes and their Development, Basque Country University, San Sebastián, 20018, Spain.
Robert M SapolskyDepartment of Biological Sciences, Stanford University, Stanford, CA, 94305, USA.
Stanford University · USUniversity of the Basque Country · ES

Funding

Neuroimmune Signaling in Neural TransplantationR01NS076756 · NINDS · STANFORD UNIVERSITY · PI PALMER, THEO D · 2012 to 2016
$3.1M
Integrin/ECM gating of adult neural stem cell activityR01MH085911 · NIMH · STANFORD UNIVERSITY · PI PALMER, THEO D · 2010 to 2014
$2.0M
Neural Stem Cell Dysfunction in Delayed Radiation InjuryR01NS045113 · NINDS · STANFORD UNIVERSITY · PI PALMER, THEO D · 2003 to 2006
$1.5M
NIMH NIH HHS R01 MH085911NINDS NIH HHS R01 NS045113NINDS NIH HHS R01 NS076756
6 · The paper itself

Abstract

Chronic stress is a recognized risk factor for psychiatric and psychological disorders and a potent modulator of adult neurogenesis. Numerous studies have shown that during stress, neurogenesis decreases; however, during the recovery from the stress, neurogenesis increases. Despite the increased number of neurons born after stress, it is unknown if the function and morphology of those neurons are altered. Here we asked whether neurons in adult mice, born during the final 5 days of chronic social stress and matured during recovery from chronic social stress, are similar to neurons born with no stress conditions from a quantitative, functional and morphological perspective, and whether those neurons are uniquely adapted to respond to a subsequent stressful challenge. We observed an increased number of newborn neurons incorporated in the dentate gyrus of the hippocampus during the 10-week post-stress recovery phase. Interestingly, those new neurons were more responsive to subsequent chronic stress, as they showed more of a stress-induced decrease in spine density and branching nodes than in neurons born during a non-stress period. Our results replicate findings that the neuronal survival and incorporation of neurons in the adult dentate gyrus increases after chronic stress and suggest that such neurons are uniquely adapted in the response to future social stressors. This finding provides a potential mechanism for some of the long-term hippocampal effects of stress.

Indexed as

Age FactorsAnimalsBrainDentate GyrusHippocampusMaleMiceNeurogenesisNeuronsStress, Psychological

Identifiers

PMID29311652
OpenAlexW2783060003

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.