دانلود مقاله ISI انگلیسی شماره 71304
ترجمه فارسی عنوان مقاله

در معرض قرار گرفتن در معرض غلظت زیست محیطی دراز مدت از زمانی که جوانان مانع از کاهش حافظه شناختی می شوند و نشانگرهای انعطاف پذیری سیناپسی را در پیری افزایش می دهند

عنوان انگلیسی
Long-term exposure to environmental enrichment since youth prevents recognition memory decline and increases synaptic plasticity markers in aging
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
71304 2008 8 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Neurobiology of Learning and Memory, Volume 90, Issue 3, October 2008, Pages 511–518

ترجمه کلمات کلیدی
موش صحرایی غنی سازی محیط زیست، حافظه شیء شناخت، نوروژنز، سیناپتوزوم ها، سیناپتوفیزین
کلمات کلیدی انگلیسی
Aged rats; Environmental enrichment; Object-recognition memory; Neurogenesis; Synaptosomes; Synaptophysin

چکیده انگلیسی

Aging-associated brain changes include functional alterations that are usually related with memory decline. Epidemiological reports show that a physically and intellectually active life provides a protective effect on this decline and delays the onset of several neurodegenerative diseases. The cellular mechanisms behind the behavioral-based therapies, such as environmental enrichment (EE) exposure, as a method for alleviating age-related memory impairments, are still unknown. Although some reports have shown the benefits of EE exposure in cognitive outcomes in old mice and in animals with experimental neurodegenerative conditions, the effects of lifelong animal exposure to EE have not been explored in detail. In the present work we tested in a rat model the effects of intermittent lifelong exposure since youth to EE on behavioral performance, object recognition memory and anxiety level, as well as on some morphological and biochemical markers of brain plasticity such as hippocampal neurogenesis, synaptophysin content and synaptic morphology. We found that environmental factors have a positive impact on short-memory preservation, as well as on the maintenance of synapses and in the increase in number of new generated neurons within the hippocampus during aging.