کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4324315 1613876 2014 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Neuroprotective effects of hypothermia on synaptic actin cytoskeletal changes induced by perinatal asphyxia
ترجمه فارسی عنوان
اثرات نوروپاتیک هیپوترمی بر تغییرات سیتو اسکلتی آکتین سیناپسی ناشی از آسفیکسی پریناتال
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
چکیده انگلیسی


• Perinatal asphyxia is a serious complication with high mortality and morbidity.
• Rat model for perinatal asphyxia is used in this study.
• We combine different techniques to study the synaptic cytoskeletal alterations.
• We report that hypothermia has a neuroprotective effect on synaptic fine arquitecture.
• These findings can help for improving a clinical use of hypothermia in PA patients.

Cerebral hypoxia–ischemia damages synaptic proteins, resulting in cytoskeletal alterations, protein aggregation and neuronal death. In the previous works, we have shown neuronal and synaptic changes in rat neostriatum subjected to hypoxia that leads to ubi-protein accumulation. Recently, we also showed that, changes in F-actin organization could be related to early alterations induced by hypoxia in the Central Nervous System. However, little is known about effective treatment to diminish the damage. The main aim of this work is to study the effects of birth hypothermia on the actin cytoskeleton of neostriatal post-synaptic densities (PSD) in 60 days olds rats by immunohistochemistry, photooxidation and western blot. We used 2 different protocols of hypothermia: (a) intrahypoxic hypothermia at 15 °C and (b) post-hypoxia hypothermia at 32 °C. Consistent with previous data at 30 days, staining with phalloidin–Alexa488 followed by confocal microscopy analysis showed an increase of F-actin fluorescent staining in the neostriatum of hypoxic animals. Correlative photooxidation electron microscopy confirmed these observations showing an increment in the number of mushroom-shaped F-actin staining spines in neostriatal excitatory synapses in rats subjected to hypoxia. In addition, western blot revealed β-actin increase in PSDs in hypoxic animals. The optic relative density measurement showed a significant difference between controls and hypoxic animals. When hypoxia was induced under hypothermic conditions, the changes observed in actin cytoskeleton were blocked. Post-hypoxic hypothermia showed similar answer but actin cytoskeleton modifications were not totally reverted as we observed at 15 °C. These data suggest that the decrease of the body temperature decreases the actin modifications in dendritic spines preventing the neuronal death.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1563, 14 May 2014, Pages 81–90
نویسندگان
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