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慢性热量限制可减少创伤性脑损伤大鼠模型的组织损伤并改善空间记忆。

Chronic caloric restriction reduces tissue damage and improves spatial memory in a rat model of traumatic brain injury.

机构信息

Program in Neuroscience and Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, Florida 32306-4300, USA.

出版信息

J Neurosci Res. 2010 Oct;88(13):2933-9. doi: 10.1002/jnr.22443.

DOI:10.1002/jnr.22443
PMID:20544832
Abstract

Although it has been known for some time that chronic caloric or dietary restriction reduces the risk of neurodegenerative disorders and injury following ischemia, the possible role of chronic restriction in improving outcomes after traumatic brain injury (TBI) has not been previously studied. Therefore, 2-month-old male Sprague-Dawley rats were divided into two dietary groups, an ad libitum fed group (AL) and a caloric-restriction group (CR) that was provided with 70% of the food intake of AL rats (n = 10/group). After 4 months, a weight-drop device (300 g) was used to produce a 2-mm bilateral medial frontal cortex contusion following craniotomy. Additional animals in each dietary group (n = 10) were used as sham-operated controls. The CR diet resulted in body weights that were reduced by 30% compared with AL controls. Not only did CR decrease the size of the cortical lesion after injury, there were marked improvements in spatial memory as measured by Morris water maze that included an increase in the number of animals successfully finding the platform as well as significantly reduced time to finding the hidden platform. Western analysis, used to examine the expression of proteins that play a role in neuronal survival, revealed significant increases in brain-derived neurotrophic factor (BDNF) in the cortical region around the site of injury and in the hippocampus in CR rats after injury. These findings suggest that molecular mechanisms involved in cell survival may play a role in reducing tissue damage and improving cognition after TBI and that these mechanisms can be regulated by dietary interventions.

摘要

虽然人们已经知道长期热量或饮食限制可以降低神经退行性疾病和缺血后损伤的风险,但慢性限制在改善创伤性脑损伤 (TBI) 后的结果方面的可能作用尚未得到研究。因此,将 2 月龄雄性 Sprague-Dawley 大鼠分为两组饮食组,自由进食组 (AL) 和热量限制组 (CR),后者提供的食物摄入量为 AL 大鼠的 70%(每组 n = 10)。4 个月后,使用重量下降装置(300 g)在开颅术后产生双侧额皮质 2 mm 挫伤。每组中的其他动物(n = 10)用作假手术对照。CR 饮食导致体重比 AL 对照组减轻 30%。CR 不仅减少了损伤后的皮质病变大小,而且在空间记忆方面也有明显改善,表现为成功找到平台的动物数量增加,以及找到隐藏平台的时间明显减少。用于检查在神经元存活中起作用的蛋白质表达的 Western 分析表明,CR 大鼠在损伤部位周围的皮质区域和海马体中,脑源性神经营养因子 (BDNF) 的表达显著增加。这些发现表明,参与细胞存活的分子机制可能在减轻 TBI 后的组织损伤和改善认知方面发挥作用,并且这些机制可以通过饮食干预来调节。

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