ABSTRACT
Studies have found that early traumatic experience significantly increases the risk of posttraumatic stress disorder (PTSD). Gamma-aminobutyric acid (GABA) deficits were proposed to be implicated in development of PTSD, but the alterations of GABA receptor A (GABAAR) subunits induced by early traumatic stress have not been fully elucidated. Furthermore, previous studies suggested that exercise could be more effective than medications in reducing severity of anxiety and depression but the mechanism is unclear. This study used inescapable foot-shock to induce PTSD in juvenile rats and examined their emotional changes using open-field test and elevated plus maze, memory changes using Morris water maze, and the expression of GABAAR subunits (γ2, α2, and α5) in subregions of the brain in the adulthood using western blotting and immunohistochemistry. We aimed to observe the role of GABAAR subunits changes induced by juvenile trauma in the pathogenesis of subsequent PTSD in adulthood. In addition, we investigated the protective effects of exercise for 6 weeks and benzodiazepine (clonazepam) for 2 weeks. This study found that juvenile traumatic stress induced chronic anxiety and spatial memory loss and reduced expression of GABAAR subunits in the adult rat brains. Furthermore, exercise led to significant improvement as compared to short-term BZ treatment.
Subject(s)
Brain/metabolism , Receptors, GABA-A/metabolism , Stress Disorders, Post-Traumatic/metabolism , Stress Disorders, Post-Traumatic/psychology , Animals , Anxiety , Disease Models, Animal , Electroshock , Male , Protein Subunits/metabolism , Rats , Rats, Wistar , Spatial MemoryABSTRACT
This study examined the heat shock protein 70 (HSP70) expression in hippocampal CA3 subfield of rats in different chronic stress models. The chronic restraint stress (CRS) and the chronic mild stress (CMS) models were used in this study. Observation of exploratory behavior in an open field test indicated stress level. The expression of HSP70 in hippocampal CA3 subfield was measured by immunohistochemical methods. The results showed that the number of quadrant crossing in both CRS and CMS groups decreased more than that of the control (P < 0.01). CRS group crossing decreased more than CMS group. Damage in the hippocampus of the CMS group occurred later and to a less extent than that of the CRS group. Compared with CMS group, the expression of HSP70 was greater in the CRS group. Moreover, increased stress duration enhanced these effects. These results show that the CRS model affects both exploratory behavior and HSP70 expression in the hippocampus more dramatically than the CMS model.
Subject(s)
HSP70 Heat-Shock Proteins/metabolism , Hippocampus/metabolism , Stress, Physiological/metabolism , Animals , Exploratory Behavior/physiology , Hippocampus/cytology , Male , Pyramidal Cells/cytology , Rats , Rats, WistarABSTRACT
This article reviewed information related to the apoptosis of breast cancer cells. Breast cancer is a common malignant tumor in women. Apoptosis is related to the response and resistance to treatment in breast cancer. Here we summarized and integrated the data on apoptosis and its role in the development, prognosis, and treatment of breast cancer. Further study on apoptosis in breast cancer can help find more candidates for predictors and indices of response. Such study will also develop treatment regimens that are tailored to individual tumors and thereby maximize survival.
