Ziprasidone ameliorates anxiety-like behaviors in a rat model of PTSD and up-regulates neurogenesis in the hippocampus and hippocampus-derived neural stem cells

التفاصيل البيبلوغرافية
العنوان: Ziprasidone ameliorates anxiety-like behaviors in a rat model of PTSD and up-regulates neurogenesis in the hippocampus and hippocampus-derived neural stem cells
المؤلفون: Lei Wang, Yunchun Chen, Fen Xue, Ling Liu, Fan Yang, Zhengwu Peng, Rui-Guo Zhang, Fang Kuang, Qingrong Tan, Huaning Wang, Yi-huan Chen
المصدر: Behavioural Brain Research. 244:1-8
بيانات النشر: Elsevier BV, 2013.
سنة النشر: 2013
مصطلحات موضوعية: Male, Cell Survival, MAP Kinase Signaling System, medicine.drug_class, Neurogenesis, Hippocampus, Atypical antipsychotic, Hippocampal formation, Neuroprotection, Piperazines, Stress Disorders, Post-Traumatic, Behavioral Neuroscience, Neural Stem Cells, In vivo, Nitriles, Butadienes, medicine, Animals, Ziprasidone, Protein Kinase Inhibitors, Cells, Cultured, Cell Proliferation, Neural stem cell, Rats, Up-Regulation, Thiazoles, Anti-Anxiety Agents, Psychology, Neuroscience, medicine.drug
الوصف: Ziprasidone, a widely used atypical antipsychotic drug, has been demonstrated to have therapeutic effects in patients with post-traumatic stress disorder (PTSD), but its underlying mechanisms remain poorly understood. One possible explanation is that the neuroprotective and neurogenetic actions of ziprasidone can attenuate the neuronal apoptosis which occurs in the hippocampus. To test this hypothesis, the present study was designed to assess the effects of ziprasidone treatment on anxiety-like behaviors, hippocampal neurogenesis, and in vivo/in vitro expression of pERK1/2 and Bcl-2 in male Sprague-Dawley rats. The methodology involved 3 different experiments, and the investigations also included the assessment of U0126 interference in ziprasidone treatment. It was found that the in vivo, administration of ziprasidone not only reversed the anxiety-like behaviors in rats that exposed to an enhanced single prolonged stress paradigm, but also restored the proliferation and the protein expression of pERK1/2 and Bcl-2 in the hippocampus of these rats. Also, mild concentrations of ziprasidone promoted the in vitro proliferation of hippocampal-derived neural stem cells (NSCs) and increased the levels of pERK1/2 and Bcl-2 in NSCs. Interestingly, the observed effects of ziprasidone were inhibited by U0126. These data support the use of ziprasidone for the treatment of PTSD and indicate that the changes in the ERK1/2 signaling cascade may play a critical role in the pathophysiology of PTSD and its treatment modalities. Further investigations are needed to elucidate the detailed signal cascades involved in the pathophysiology of stress-related disorders, and confirm the efficacy of ziprasidone in anti-PTSD treatment.
تدمد: 0166-4328
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b56853e4ca1c02cfabb81d85fdc4a1
https://doi.org/10.1016/j.bbr.2013.01.032
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....f0b56853e4ca1c02cfabb81d85fdc4a1
قاعدة البيانات: OpenAIRE