Evidence map›Paper›PMID 29257131›Full record

ArticleMolecular psychiatry2018

Differential effects of chronic stress in young-adult and old female mice: cognitive-behavioral manifestations and neurobiological correlates.

A Lotan, T Lifschytz, G Wolf, S Keller, H Ben-Ari, P Tatarsky, N Pillar, K Oved, J Sharabany, T K Merzel and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
  2. The Impact of Adverse Childhood Experiences and Resilience on Medical Student Well-Being.Academic psychiatry : the journal of the American Association of Directors of Psychiatric Residency Training and the Association for Academic Psychiatry · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. SubcutaneousNeurobiology of stress · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Hippocampal deficits in neurodevelopmental disorders.Neurobiology of learning and memory · 2019
    Review
  18. Review
  19. Article
  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

18 authors.

A LotanBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
T LifschytzBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
G WolfBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
S KellerBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
H Ben-AriBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
P TatarskyBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
N PillarDepartment of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
K OvedDepartment of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
J SharabanyGonda Brain Research Center, Bar-Ilan University, Ramat-Gan, Israel.
T K MerzelDepartment of Developmental Biology and Cancer Research, Hadassah-Hebrew University Medical School, Jerusalem, Israel.
T MatsumotoDepartment of Psychiatry and Neurosciences, Institute of Biomedical and Health Sciences, Hiroshima University, Minami-ku, Hiroshima, Japan.
Y YamawakiDepartment of Cellular and Molecular Pharmacology, Institute of Biomedical and Health Sciences, Hiroshima University, Minami-ku, Hiroshima, Japan.
B MernickBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
E AvidanBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
S YamawakiDepartment of Psychiatry and Neurosciences, Institute of Biomedical and Health Sciences, Hiroshima University, Minami-ku, Hiroshima, Japan.
A WellerGonda Brain Research Center, Bar-Ilan University, Ramat-Gan, Israel.
N ShomronDepartment of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
B LererBiological Psychiatry Laboratory, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stress-related psychopathology is highly prevalent among elderly individuals and is associated with detrimental effects on mood, appetite and cognition. Conversely, under certain circumstances repeated mild-to-moderate stressors have been shown to enhance cognitive performance in rodents and exert stress-inoculating effects in humans. As most stress-related favorable outcomes have been reported in adolescence and young-adulthood, this apparent disparity could result from fundamental differences in how aging organisms respond to stress. Furthermore, given prominent age-related alterations in sex hormones, the effect of chronic stress in aging females remains a highly relevant yet little studied issue. In the present study, female C57BL/6 mice aged 3 (young-adult) and 20-23 (old) months were subjected to 8 weeks of chronic unpredictable stress (CUS). Behavioral outcomes were measured during the last 3 weeks of the CUS protocol, followed by brain dissection for histological and molecular end points. We found that in young-adult female mice, CUS resulted in decreased anxiety-like behavior and enhanced cognitive performance, whereas in old female mice it led to weight loss, dysregulated locomotion and memory impairment. These phenotypes were paralleled by differential changes in the expression of hypothalamic insulin and melanocortin-4 receptors and were consistent with an age-dependent reduction in the dynamic range of stress-related changes in the hippocampal transcriptome. Supported by an integrated microRNA (miRNA)-mRNA expression analysis, the present study proposes that, when confronted with ongoing stress, neuroprotective mechanisms involving the upregulation of neurogenesis, Wnt signaling and miR-375 can be harnessed more effectively during young-adulthood. Conversely, we suggest that aging alters the pattern of immune activation elicited by stress. Ultimately, interventions that modulate these processes could reduce the burden of stress-related psychopathology in late life.

Indexed as

Age FactorsAnimalsAnxietyBehavior, AnimalBrainCognitionFemaleHippocampusMiceMice, Inbred C57BLNeurobiologyNeurogenesisStress, Psychological

Identifiers

PMID29257131

What OpenQuestion holds

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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 OpenQuestion graph.