昼夜节律在缺血性卒中预后中的临床前评估。

P. Kamat, Mohammad B. Khan, Kristofer Wood, Shahneela Siddiqui, D. Rudic, K. Dhandapani, Jennifer Waller, D. Hess
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引用次数: 5

摘要

中风是全世界致残和死亡的主要原因。有证据表明,中风有昼夜节律,早晨(上午6点至10点)是发生的高峰。然而,目前尚不清楚梗死的大小和卒中的结果是否在24小时内也会发生变化。我们假设脑梗死的大小和中风的结果会在小鼠缝合闭塞模型中显示昼夜变化。取7 ~ 8月龄C57BL/6J小鼠(n =10 ~ 12只/组),在ZT0、ZT6、ZT12、Z18授时后24h天的不同时间点进行大脑中动脉闭塞(MCAO)治疗60分钟。在闭塞后基线和闭塞后24h再次用激光散斑造影监测脑血流。24h和48h采用Bederson评分法观察神经功能缺损。角点法检测脑卒中小鼠48h时单侧感觉和运动功能的异常。脑梗死后48h行2,3,5-tryphenyltetrazolium chloride染色,用NIH-Image J软件定量梗死面积。我们没有发现在任何时间点的脑血流量有显著差异。在ZT18(午夜)时段,Bederson评分从24小时(1.82±1.11)到48小时(1.10±0.12),神经功能缺损显著降低(p = 0.0025),但在48小时,两组间无差异。在角落测试中,我们发现,与完全清醒(5.5±4.06)(午夜,ZT18)和ZT0 (6 am, 4.8±0.97,p = 0.0087)相比,中午/ZT06(9.5±1.06)的右转偏好显著更高(p = 0.0348)。同样,缺血小鼠在睡眠(ZT06,中午)期间的梗死体积(35.22±20.77)明显高于午夜/ZT18期间完全清醒时的(15.68±7.54)(p = 0.0220)。这是第一个证明小鼠在睡眠期间(中午/ZT06)比在清醒期间(午夜/ZT18)有更大的梗死和更差的短期结果的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical evaluation of circadian rhythm in ischemic stroke outcomes.
Stroke is a leading cause of disability and death worldwide. There is evidence that there is a circadian rhythm in stroke with peak occurrence in the morning (6 to 10 am). However, it is not clear if the size of infarcts and the outcome of stroke also varies during the 24-hour period. We hypothesized that the size of cerebral infarct and outcome from stroke would show circadian variation in a mouse suture occlusion model. Seven to eight-month-old C57BL/6J (n =10-12 mice/group) mice were randomly assigned to undergo middle cerebral artery occlusion (MCAO) for 60 minutes at different time points during the 24h day following zeitgeber time at ZT0, ZT6, ZT12, and Z18. Cerebral blood flow was monitored by Laser Speckle Contrast Imaging at baseline after occlusion, and again at 24h post-occlusion. Neurological deficit was observed by using Bederson score at 24h and 48h. The corner test was used to detect unilateral abnormalities in sensory and motor functions in the stroke mice at 48h. To estimate brain infarction, 2,3,5-tryphenyltetrazolium chloride staining was performed 48h after stroke and the infarct area was quantified using NIH-Image J software. We did not find a significant difference in cerebral blood flow at any time point. There was a significant decrease in neurological deficit as assessed using the Bederson Score from 24h (1.82 ± 1.11) to 48h (1.10 ± 0.12) in the ZT18 (midnight) period (p = 0.0025), however there were no differences between groups at 48h. In the corner test, we found right turn preference significantly higher (p = 0.0348) at noon/ZT06 (9.5 ± 1.06) compared to the fully awake (5.5 ± 4.06) (midnight, ZT18) period and ZT0 (6 am, 4.8 ± 0.97, p = 0.0087). Similarly, the infarction volume was significantly higher (p = 0.0220) during the sleep (ZT06, noon) period (35.22 ± 20.77) than when the ischemic mice were fully awake during the midnight/ZT18 period (15.68 ± 7.54). This is the first report demonstrating that mice have larger infarcts and worse short-term outcomes during their sleep period (noon/ZT06) than during their awake period (midnight/ZT18).
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