ArticlePloS one2007
Moderate neonatal stress decreases within-group variation in behavioral, immune and HPA responses in adult mice.
Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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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.
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Who cites it
21 citing papers in PubMed, 59 citations in OpenAlex.
- Long-term consequences of reduced availability and compensatory supplementation of sialylated HMOs on cognitive capabilities.Frontiers in cellular neuroscience · 2023Article
- Sialylated human milk oligosaccharides program cognitive development through a non-genomic transmission mode.Molecular psychiatry · 2021Article
- Aberrant Early in Life Stimulation of the Stress-Response System Affects Emotional Contagion and Oxytocin Regulation in Adult Male Mice.International journal of molecular sciences · 2021Article
- Article
- Brain-Immune Alterations and Mitochondrial Dysfunctions in a Mouse Model of Paediatric Autoimmune Disorder Associated with Streptococcus: Exacerbation by Chronic Psychosocial Stress.Journal of clinical medicine · 2019Article
- Developmental corticosterone treatment does not program immune responses in zebra finches (Journal of experimental zoology. Part A, Ecological and integrative physiology · 2017Article
- Neonatal corticosterone administration in rodents as a tool to investigate the maternal programming of emotional and immune domains.Neurobiology of stress · 2017Article
- Mice repeatedly exposed to Group-A β-Haemolytic Streptococcus show perseverative behaviors, impaired sensorimotor gating, and immune activation in rostral diencephalon.Scientific reports · 2015Article
- The Snark was a Boojum - reloaded.Frontiers in zoology · 2015Review
- Enrichment with wood blocks does not affect toxicity assessment in an exploratory toxicology model using Sprague-Dawley rats.Journal of the American Association for Laboratory Animal Science : JAALAS · 2014Article
- Prenatal corticosterone and adolescent URB597 administration modulate emotionality and CB1 receptor expression in mice.Psychopharmacology · 2014Article
- Behavioral responses to acute and sub-chronic administration of the synthetic cannabinoid JWH-018 in adult mice prenatally exposed to corticosterone.Neurotoxicity research · 2013Article
- The Directive 2010/63/EU on animal experimentation may skew the conclusions of pharmacological and behavioural studies.Scientific reports · 2013Article
- Article
- On the incongruity between developmental plasticity and methodological rigidity.Frontiers in behavioral neuroscience · 2012Article
- The Adaptive Calibration Model of stress responsivity.Neuroscience and biobehavioral reviews · 2011Review
- Update in the methodology of the chronic stress paradigm: internal control matters.Behavioral and brain functions : BBF · 2011Review
- Critical age windows for neurodevelopmental psychiatric disorders: evidence from animal models.Neurotoxicity research · 2011Review
- Perinatal flavour learning and adaptation to being weaned: all the pig needs is smell.PloS one · 2011Article
- Staging perspectives in neurodevelopmental aspects of neuropsychiatry: agents, phases and ages at expression.Neurotoxicity research · 2010Review
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe significance of behavioral neuroscience and the validity of its animal models of human pathology largely depend on the possibility to replicate a given finding across different laboratories. Under the present test and housing conditions, this axiom fails to resist the challenge of experimental validation. When several mouse strains are tested on highly standardized behavioral test batteries in different laboratories, significant strain x lab interactions are often detected. This limitation, predominantly due to elevated within-group variability observed in control subjects, increases the number of animals needed to address fine experimental questions. Laboratory rodents display abnormal stress and fear reactions to experimental testing, which might depend on the discrepancy between the stability of the neonatal environment and the challenging nature of the adult test and housing conditions. METHODOLOGY/PRINCIPAL
findingsStimulating neonatal environments (e.g. brief maternal separations, increased foraging demands or maternal corticosterone supplementation) reduce stress and fear responses in adulthood. Here we tested whether reduced fearfulness associated with experimental testing would also reduce inter-individual variation. In line with our predictions, we show that a moderate elevation in neonatal corticosterone through maternal milk significantly reduces fear responses and inter-individual variability (average 44%) in adult mouse offspring. CONCLUSIONS/SIGNIFICANCE: We observed reduced variation in pain perception, novelty preference, hormonal stress response and resistance to pathogen infection. This suggests that the results of this study may apply to a relatively broad spectrum of neuro-behavioral domains. Present findings encourage a reconsideration of the basic principles of neonatal housing systems to improve the validity of experimental models and reduce the number of animals used.
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Registered trials
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.