کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6257296 1612950 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research reportChronic social isolation decreases glutamate and glutamine levels and induces oxidative stress in the rat hippocampus
ترجمه فارسی عنوان
گزارش تحقیقاتی جداسازی اجتماعی کاهش سطح گلوتامات و گلوتامین و ایجاد استرس اکسیداتیو در هیپوکامپ موش صحرایی
کلمات کلیدی
انزوای اجتماعی، استرس اکسیداتیو، هیپوکامپ، یکپارچگی نورون-گلویی، پایداری عصبی،
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
چکیده انگلیسی


- SI increased anxiety level but impaired social interaction and spatial working memory.
- SI decreased levels of glutamate, glutamine, and phosphocreatine in the hippocampus.
- SI increased levels of H2O2 in caudate putamen and hippocampus.
- SI decreased activities of some antioxidant enzymes.

Social isolation (SI) rearing of rodents is a developmental manipulation, which is commonly compared with the psychological stressors in humans as it produces several behavioral outcomes similar to those observed in humans with early life stress. To explain the SI-induced behavioral outcomes, animal studies have been performed to examine the dopaminergic and glutamatergic systems in the brain. In this study, we measured possible changes in levels of glutamate and glutamine of SI-rats using proton magnetic resonance spectroscopy. We also assessed the oxidative stress parameters in certain brain regions to see if glutamate and/or glutamine changes, if any, are associated with oxidative stress. SI rearing for 8 weeks decreased the activities of antioxidant enzymes catalase, glutathione peroxidase, superoxide dismutase, and the total antioxidant capacity, but increased levels of hydrogen peroxide, in certain brain regions, of which prefrontal cortex and hippocampus were most vulnerable. It also decreased levels of glutamate, glutamine, N-acetyl-l-aspartate (NAA), and phosphocreatine in the dorsal hippocampus, but not in the cerebral cortex. Decreased phosphocreatine and NAA indicate energy metabolism deficit in brain cells; the latter also suggests the neuronal viability was inhibited. Decreased glutamate and glutamine may suggest the neuron-glial integrity was implicated by chronic SI. These neurochemical and biochemical changes may contribute to the SI-induced behavioral abnormalities including a high level of anxiety, social interaction deficit, and impaired spatial working memory shown in this study.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Behavioural Brain Research - Volume 282, 1 April 2015, Pages 201-208
نویسندگان
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