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A single exposure to immobilization causes long-lasting pituitary-adrenal and behavioral sensitization to mild stressors
Affiliation:1. Institut de Neurociències, Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain;2. Unitat de Fisiologia Animal (Facultat de Biociències), Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain;3. Unitat de Psicobiologia (Facultat de Psicologia), Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain;1. Mother Infant Research Institute at Tufts Medical Center, Boston, Massachusetts;2. Tufts Clinical and Translational Science Institute, Boston, Massachusetts;1. Department of Biobehavioral Health, Penn State University, University Park, PA, USA;2. Department of Psychology, Neuroscience Program, Weiss Hall, Temple University, Philadelphia, PA, USA;1. Department of Physics, Tripura University, Suryamaninagar 799022, Tripura, India;2. Department of Physics, Women''s College, Agartala 799001, Tripura, India;1. Department of Internal Medicine, Vaccine Institute, Hacettepe University School of Medicine, Ankara, Turkey;2. Department of Infectious Diseases, Vaccine Institute, Hacettepe University School of Medicine, Ankara, Turkey
Abstract:We have previously reported that a single exposure to immobilization (IMO) in rats causes a long-term desensitization of the hypothalamic-pituitary-adrenal (HPA) response to the same (homotypic) stressor. Since there are reports showing that a single exposure to other stressors causes sensitization of the HPA response to heterotypic stressors and increases anxiety-like behavior, we studied in the present work the long-term effects of IMO on behavioral and HPA response to mild superimposed stressors. In Experiments 1 and 2, adult male Sprague–Dawley rats were subjected to 2 h of IMO and then exposed for 5 min to the elevated plus-maze (EPM) at 1, 3 or 7 days after IMO. Blood samples were taken at 15 min after initial exposure to the EPM. Increases in anxiety-like behavior and HPA responsiveness to the EPM were found at all times post-IMO. Changes in the resting levels of HPA hormones did not explain the enhanced HPA responsiveness to the EPM (Experiment 3). In Experiments 4 and 5, we studied the effects of a single exposure to a shorter session of IMO (1 h) on behavioral and HPA responses to a brief and mild session of foot-shocks done 10 days after IMO. Neither previous IMO nor exposure to shocks in control rats modified behavior in the EPM. However, a brief session of shocks in previously IMO-exposed rats dramatically increased anxiety in the EPM. HPA and freezing responses to shocks were similar in control and previous IMO groups. Therefore, a single exposure to IMO appears to induce long-lasting HPA and behavioral sensitization to mild superimposed stressors, although the two responses are likely to be at least partially independent. Long-term effects of IMO on the susceptibility to stress-induced endocrine and emotional disturbances may be relevant to the characterization of animal models of post-traumatic stress.
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