Comparative neurobiology of vigilance and stress adaptation systems in wild and laboratory rodents (Rattus norvegicus)

Although chronic stress is typically associated with disease and negative outcomes, wild animals often survive—and even thrive—in environments marked by recurring threats. In this study, we investigated neurobiological differences in vigilance-associated and stress-coping systems, as well as resilience, in wild and laboratory-bred rats ( Rattus norvegicus ) to explore potential survival-related adaptations in wild populations. Consistent with previous findings, wild rats exposed to chronic environmental stressors exhibited heightened hypothalamic-pituitary-adrenal axis activity, evidenced by enlarged adrenal glands and elevated fecal metabolites of glucocorticoids. Brains were processed using thionin staining for neural and glial cell counts and immunohistochemistry for immunoreactive targets. Wild rats exhibited neuronal and glial cell modifications in vigilance-related cortical regions, including the auditory and piriform cortices. Additional adaptations included increased glial cell density in the lateral habenula—a region implicated in coping appraisal—and enhanced microvascular density in the hippocampus. These findings underscore the value of incorporating wild animals exposed to naturalistic stressors into the study of adaptive and maladaptive stress responses. Integrating wild and laboratory models may yield translational insights for developing therapeutic strategies targeting stress- and anxiety-related disorders.

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Publication Details

Journal
Frontiers in Ethology
Published
2025-09-23
DOI
https://doi.org/10.3389/fetho.2025.1644812
Primary Topic
Stress Responses and Cortisol
Type
article
Field-Weighted Citation Impact
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article

Comparative neurobiology of vigilance and stress adaptation systems in wild and laboratory rodents (Rattus norvegicus)

Gabriella Handford, Richard Hunter, Kelly Lambert, Brendan Crockett et al.
Frontiers in Ethology
Stress Responses and Cortisol
article

Comparative neurobiology of vigilance and stress adaptation systems in wild and laboratory rodents (Rattus norvegicus)

Gabriella Handford, Richard Hunter, Kelly Lambert, Brendan Crockett, Joanna Jacob, Troy Richter, Arunachalam Narayanan, Alexander Wagner, Olivia Harding, Paean Luby, Jonathan Richardson, Molly Kent, Sarah Catherine Hartvigsen, Isabel Dilandro, Andrés Mauco
article en

Abstract

Although chronic stress is typically associated with disease and negative outcomes, wild animals often survive—and even thrive—in environments marked by recurring threats. In this study, we investigated neurobiological differences in vigilance-associated and stress-coping systems, as well as resilience, in wild and laboratory-bred rats ( Rattus norvegicus ) to explore potential survival-related adaptations in wild populations. Consistent with previous findings, wild rats exposed to chronic environmental stressors exhibited heightened hypothalamic-pituitary-adrenal axis activity, evidenced by enlarged adrenal glands and elevated fecal metabolites of glucocorticoids. Brains were processed using thionin staining for neural and glial cell counts and immunohistochemistry for immunoreactive targets. Wild rats exhibited neuronal and glial cell modifications in vigilance-related cortical regions, including the auditory and piriform cortices. Additional adaptations included increased glial cell density in the lateral habenula—a region implicated in coping appraisal—and enhanced microvascular density in the hippocampus. These findings underscore the value of incorporating wild animals exposed to naturalistic stressors into the study of adaptive and maladaptive stress responses. Integrating wild and laboratory models may yield translational insights for developing therapeutic strategies targeting stress- and anxiety-related disorders.

Frontiers in EthologyVol. 4
Boston University (US), University of Richmond (US), Virginia Military Institute (US), University of Massachusetts Boston (US)
Openalex Percentile: Top 72%
Stress Responses and Cortisol
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