Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models
- PMID: 19616355
- DOI: 10.1016/j.bandc.2009.06.003
Investigations of HPA function and the enduring consequences of stressors in adolescence in animal models
Abstract
Developmental differences in hypothalamic-pituitary-adrenal (HPA) axis responsiveness to stressors and ongoing development of glucocorticoid-sensitive brain regions in adolescence suggest that similar to the neonatal period of ontogeny, adolescence may also be a sensitive period for programming effects of stressors on the central nervous system. Although research on this period of life is scarce compared to early life and adulthood, the available research indicates that effects of stress exposure during adolescence differ from, and may be longer-lasting than, effects of the same stress exposure in adulthood. Research progress in animal models in this field is reviewed including HPA function and the enduring effects of stress exposures in adolescence on sensitivity to drugs of abuse, learning and memory, and emotional behaviour in adulthood. The effects of adolescent stress depend on a number of factors, including the age, gender, the duration of stress exposure, the type of stressor, and the time between stress exposure and testing.
2009 Elsevier Inc. All rights reserved.
Similar articles
-
Adolescent development, hypothalamic-pituitary-adrenal function, and programming of adult learning and memory.Prog Neuropsychopharmacol Biol Psychiatry. 2010 Jun 30;34(5):756-65. doi: 10.1016/j.pnpbp.2009.09.019. Epub 2009 Sep 25. Prog Neuropsychopharmacol Biol Psychiatry. 2010. PMID: 19782715 Review.
-
HPA function in adolescence: role of sex hormones in its regulation and the enduring consequences of exposure to stressors.Pharmacol Biochem Behav. 2007 Feb;86(2):220-33. doi: 10.1016/j.pbb.2006.07.012. Epub 2006 Aug 8. Pharmacol Biochem Behav. 2007. PMID: 16901532 Review.
-
An animal model of social instability stress in adolescence and risk for drugs of abuse.Physiol Behav. 2010 Feb 9;99(2):194-203. doi: 10.1016/j.physbeh.2009.01.014. Epub 2009 Jan 24. Physiol Behav. 2010. PMID: 19419678 Review.
-
Long-lasting, sex- and age-specific effects of social stressors on corticosterone responses to restraint and on locomotor responses to psychostimulants in rats.Horm Behav. 2005 Jun;48(1):64-74. doi: 10.1016/j.yhbeh.2005.01.008. Horm Behav. 2005. PMID: 15919386
-
A single exposure to immobilization causes long-lasting pituitary-adrenal and behavioral sensitization to mild stressors.Horm Behav. 2008 Nov;54(5):654-61. doi: 10.1016/j.yhbeh.2008.07.003. Epub 2008 Jul 16. Horm Behav. 2008. PMID: 18675818
Cited by
-
Review: Puberty as a time of remodeling the adult response to ovarian hormones.J Steroid Biochem Mol Biol. 2016 Jun;160:2-8. doi: 10.1016/j.jsbmb.2015.05.007. Epub 2015 May 21. J Steroid Biochem Mol Biol. 2016. PMID: 26004504 Free PMC article. Review.
-
Adolescence and the ontogeny of the hormonal stress response in male and female rats and mice.Neurosci Biobehav Rev. 2016 Nov;70:206-216. doi: 10.1016/j.neubiorev.2016.05.020. Epub 2016 May 24. Neurosci Biobehav Rev. 2016. PMID: 27235079 Free PMC article. Review.
-
The effects of oxytocin on cognitive defect caused by chronic restraint stress applied to adolescent rats and on hippocampal VEGF and BDNF levels.Med Sci Monit. 2015 Jan 6;21:69-75. doi: 10.12659/MSM.893159. Med Sci Monit. 2015. PMID: 25559382 Free PMC article.
-
Stress during puberty exerts sex-specific effects on depressive-like behavior and monoamine neurotransmitters in adolescence and adulthood.Neurobiol Stress. 2022 Oct 3;21:100494. doi: 10.1016/j.ynstr.2022.100494. eCollection 2022 Nov. Neurobiol Stress. 2022. PMID: 36532376 Free PMC article.
-
Prefrontal cortical trkB, glucocorticoids, and their interactions in stress and developmental contexts.Neurosci Biobehav Rev. 2018 Dec;95:535-558. doi: 10.1016/j.neubiorev.2018.10.015. Neurosci Biobehav Rev. 2018. PMID: 30477984 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical