Complex environmental rearing enhances social salience and affects hippocampal corticotropin releasing hormone receptor expression in a sex-specific manner.
Abstract
Methods for understanding the neurocircuitry of ethologically relevant behaviors have advanced substantially; however renovations to standard animal laboratory housing, in the form of enhanced enrichment, have lagged behind. This is despite evidence that environmental enrichment (EE) reduces stress, stereotypy, and promotes healthy species typical behaviors. While many scientists express interest for increased EE as a standard for animal caging systems, there are concerns that its effects on brain, behavior, and cognition are not well characterized. In the present study, male and female Sprague-Dawley rats were housed for six weeks in either EE, Colony Nesting (CN), or Standard Housing (SD) conditions. We show that adolescent exposure to environmental complexity changed the dynamics of social interactions, sensory processing, and underlying basal stress neurocircuitry, in a sex- and enrichment-type-dependent manner. Specifically, EE and CN increased prosocial engagement and the social saliency of male and female rats while the profile of hippocampal Crhr2 expression was affected only in EE males. Hippocampal Crh was associated with anxiety-like behavior in SD males - this did not extend to EE or CN groups, nor to females. Observations such as these are an important consideration for the validity of translational research investigating the neurocircuitry of stress resiliency, and for understanding the mechanisms of psychiatric disorders. Future work must focus on characterizin…
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Beneficial effects of environmental enrichment on social behavior have been shown.
“More recently, beneficial effects of environmental enrichment on social behavior have been shown (Brenes et al., 2016; Kentner et al., 2018).”
From Effects of Maternal Deprivation and Complex Housing on Rat Social Behavior in Adolescence and Adulthood (2018) · cites this paper as Kentner et al., 2018
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Back to the future: The organizational-activational hypothesis adapted to puberty and adolescence
Schulz, K. M., Molenda-Figueira, H. A., & Sisk, C. L. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.03.010 · Cited by 587 · see citing works
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Kentner, A. C., Cryan, J. F., & Brummelte, S. (2019) · Developmental Psychobiology · doi:10.1002/dev.21775 · Cited by 64 · see citing works
Self-citationKentrop, J., Smid, C. R., Achterberg, E. J. M., van IJzendoorn, M. H., Bakermans-Kranenburg, M. J., Joëls, M., & van der Veen, R. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00193 · Cited by 41 · see citing works
“More recently, beneficial effects of environmental enrichment on social behavior have been shown (Brenes et al., 2016; Kentner et al., 2018).”
BackgroundThe Contribution of Environmental Enrichment to Phenotypic Variation in Mice and Rats.
Kentner, A. C., Speno, A. V., Doucette, J., & Roderick, R. C. (2021) · eneuro · doi:10.1523/eneuro.0539-20.2021 · Cited by 37 · see citing works
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- Authors
- Kentner, A. C., Lima, E., Migliore, M. M., Shin, J., & Scalia, S.
- Affiliations
- Massachusetts College of Pharmacy and Health Sciences (US)
- Corresponding author
- Kentner, Amanda C.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2018-01
- Volume
- 369
- Pages
- 399-411
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2769890653
- Cited by
- 23
- References
- 3
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 5 · 2019: 1 · 2018: 4
- FWCI
- 1.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- SURF
- MCPHS Faculty Development Grant
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Veterinary › Small Animals › Animal Behavior and Welfare Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- environmental enrichment, colony nesting, animal housing conditions, social salience, prosocial behavior, hippocampus, CRHR2, corticotropin-releasing factor, sex differences, anxiety-like behavior, stress resilience, Sprague-Dawley rats
- MeSH terms
- Animals, Anxiety, Corticosterone, Corticotropin-Releasing Hormone, Discrimination, Psychological, Female, Habituation, Psychophysiologic, Hippocampus, Housing, Animal, Male, Motor Activity, Random Allocation, Sex Characteristics, Social Behavior, Stress, Psychological, Rats, Sprague-Dawley, Prefrontal Cortex, Receptors, Corticotropin-Releasing Hormone, Gene Expression Regulation, Developmental, Receptor, Serotonin, 5-HT2A, Olfactory Perception
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