Posttraumatic hypothermia increases doublecortin expressing neurons in the dentate gyrus after traumatic brain injury in the rat

被引:42
作者
Bregy, Amade [1 ]
Nixon, Ryan [1 ]
Lotocki, George [1 ]
Alonso, Ofelia F. [1 ]
Atkins, Coleen M. [1 ]
Tsoulfas, Pantelis [1 ]
Bramlett, Helen M. [1 ]
Dietrich, W. Dalton [1 ]
机构
[1] Univ Miami, Dept Neurol Surg, Neurotrauma Res Ctr, Miami Project Cure Paralysis,Miller Sch Med, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
Dentate gyrus; Doublecortin; Fluid-percussion; Hypothermia; Neurogenesis; Traumatic brain injury; MICROTUBULE-ASSOCIATED PROTEIN; CONTROLLED CORTICAL IMPACT; TRANSIENT GLOBAL-ISCHEMIA; NEURAL PROGENITOR CELLS; FOCAL CEREBRAL-ISCHEMIA; NECROSIS-FACTOR-ALPHA; HIPPOCAMPAL NEUROGENESIS; SUBVENTRICULAR ZONE; ENHANCED NEUROGENESIS; ADULT RATS;
D O I
10.1016/j.expneurol.2011.12.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous studies have demonstrated that moderate hypothermia reduces histopathological damage and improves behavioral outcome after experimental traumatic brain injury (TBI). Further investigations have clarified the mechanisms underlying the beneficial effects of hypothermia by showing that cooling reduces multiple cell injury cascades. The purpose of this study was to determine whether hypothermia could also enhance endogenous reparative processes following TBI such as neurogenesis and the replacement of lost neurons. Male Sprague-Dawley rats underwent moderate fluid-percussion brain injury and then were randomized into normothermia (37 degrees C) or hypothermia (33 degrees C) treatment. Animals received injections of 5-bromo-2'-deoxyuridine (BrdU) to detect mitotic cells after brain injury. After 3 or 7 days, animals were perfusion-fixed and processed for immunocytochemistry and confocal analysis. Sections were stained for markers selective for cell proliferation (BrdU), neuroblasts and immature neurons (doublecortin), and mature neurons (NeuN) and then analyzed using non-biased stereology to quantify neurogenesis in the dentate gyrus (DG). At 7 days after TBI, both normothermic and hypothermic TBI animals demonstrated a significant increase in the number of BrdU-immunoreactive cells in the DG as compared to sham-operated controls. At 7 days post-injury, hypothermia animals had a greater number of BrdU (ipsilateral cortex) and doublecortin (ipsilateral and contralateral cortex) immunoreactive cells in the DG as compared to normothermia animals. Because adult neurogenesis following injury may be associated with enhanced functional recovery, these data demonstrate that therapeutic hypothermia sustains the increase in neurogenesis induced by TBI and this may be one of the mechanisms by which hypothermia promotes reparative strategies in the injured nervous system. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:821 / 828
页数:8
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