Resilience and vulnerability are dose-dependently related to neonatal stressors in mice
Autor: | Alessandra Berry, Giovanni Laviola, Fernando J. Santos, Simone Macrì, Oleg Granstrem, Luciano Saso, M.V. Shumilina |
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Rok vydání: | 2009 |
Předmět: |
bdnf
cognitive abilities corticosterone early experience long-term effects mouse natural antibodies neonatal stressors psychiatric disorders resilience stress vulnerability Male Time Factors Neuropsychological Tests Hippocampus Mice Behavioral Neuroscience chemistry.chemical_compound Cognition Endocrinology Corticosterone Lactation Serotonin Plasma Membrane Transport Proteins Brain medicine.anatomical_structure Corticosteroid Female Psychology Glucocorticoid medicine.drug medicine.medical_specialty medicine.drug_class Offspring Mice Inbred Strains Dopamine Internal medicine medicine Animals Autoantibodies Brain-derived neurotrophic factor Dopamine Plasma Membrane Transport Proteins Dose-Response Relationship Drug Endocrine and Autonomic Systems Brain-Derived Neurotrophic Factor Animals Newborn chemistry Serotonin Stress Psychological |
Zdroj: | Hormones and Behavior. 56:391-398 |
ISSN: | 0018-506X |
Popis: | Early life experiences have been shown to adjust cognitive abilities, stress reactivity, fear responses and immune activity in adult mammals of many species. However, whereas severe stressors have been generally associated with the emergence of hypothalamic pituitary adreno-cortical (HPA)-mediated pathology, mild neonatal stressful experiences have been traditionally associated with 'positive' effects or resilience. External stressors stimulate the HPA axis to induce a corticosterone secretion in mouse dams, which, in turn is directly transmitted to the progeny through lactation. Such corticosteroid transfer may offer a unitary mechanism whereby early low corticosterone exposure may favor resilience in the offspring and high corticosterone increase vulnerability to pathology. In this study we further investigated this hypothesis by evaluating the long-term effects of a neonatal exposure to low (33 mg/l) and high (100 mg/l) doses of corticosterone during the first 10 days of life in outbred CD-1 mice through supplementation in the maternal drinking water. Offspring attentional set-shifting abilities, central neurotrophic regulation and levels of natural auto-antibodies (na-Abs) directed to serotonin (SERT) and dopamine (DAT) transporters were assessed in adulthood. While low levels of neonatal corticosterone improved adult cognitive abilities and increased na-Abs levels directed to SERT, high doses of neonatal corticosterone reduced hippocampal BDNF levels and na-Abs directed to DAT. These findings confirm and extend our previous findings, supporting the view that both adaptive plasticity and pathological outcomes in adulthood may depend on circulating neonatal corticosterone levels and that these effects follow a U-shaped profile. |
Databáze: | OpenAIRE |
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