کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6021891 1580654 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Injury timing alters metabolic, inflammatory and functional outcomes following repeated mild traumatic brain injury
ترجمه فارسی عنوان
زمان بندی آسیب های ناشی از متابولیسم، التهاب و نتایج عملکردی پس از آسیب مغزی آسیب دیده تکراری خفیف است
کلمات کلیدی
آسیب تروماتیک مغز، متابولیسم گلوکز، آسیب تکراری، یادگیری و حافظه، نتایج کارکردی، التهاب
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی عصب شناسی
چکیده انگلیسی


- Repeated traumatic brain injuries can produce devastating results.
- Repeated injuries close together in time worsen functional and metabolic outcomes.
- Enhanced vulnerability may be mediated by impaired brain energy metabolism.

Repeated head injuries are a major public health concern both for athletes, and members of the police and armed forces. There is ample experimental and clinical evidence that there is a period of enhanced vulnerability to subsequent injury following head trauma. Injuries that occur close together in time produce greater cognitive, histological, and behavioral impairments than do injuries separated by a longer period. Traumatic brain injuries alter cerebral glucose metabolism and the resolution of altered glucose metabolism may signal the end of the period of greater vulnerability. Here, we injured mice either once or twice separated by three or 20 days. Repeated injuries that were separated by three days were associated with greater axonal degeneration, enhanced inflammatory responses, and poorer performance in a spatial learning and memory task. A single injury induced a transient but marked increase in local cerebral glucose utilization in the injured hippocampus and sensorimotor cortex, whereas a second injury, three days after the first, failed to induce an increase in glucose utilization at the same time point. In contrast, when the second injury occurred substantially later (20 days after the first injury), an increase in glucose utilization occurred that paralleled the increase observed following a single injury. The increased glucose utilization observed after a single injury appears to be an adaptive component of recovery, while mice with 2 injuries separated by three days were not able to mount this response, thus this second injury may have produced a significant energetic crisis such that energetic demands outstripped the ability of the damaged cells to utilize energy. These data strongly reinforce the idea that too rapid return to activity after a traumatic brain injury can induce permanent damage and disability, and that monitoring cerebral energy utilization may be a tool to determine when it is safe to return to the activity that caused the initial injury.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neurobiology of Disease - Volume 70, October 2014, Pages 108-116
نویسندگان
, , ,