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Kir6.1基因敲除小鼠脑梗死周围扩散性去极化波的 内源光信号成像[J]. 中山大学学报(医学科学版), 2015,36(2).
Optical Intrinsic Signal Imaging of Peri-infarct Depolarizations in Kir6.1 Knockout Mice[J]. Journal of Sun Yat-sen University (Medical Sciences), 2015, 36(2).
【目的】 观测小鼠脑梗死周围扩散性去极化波(PID)的内源光信号变化特征
了解Kir6.1基因敲除对小鼠PID的影响?【方法】 以Kir6.1基因敲除小鼠及同窝野生型小鼠各10只为研究对象
线栓法制备大脑中动脉梗死(MCAO)模型
应用四波长内源光信号(OIS)成像技术监测PID的发作情况
比较两组之间的差异?【结果】 OIS成像显示PID在空间分布上表现为由发源处向四周缓慢播散的?红蓝相间的弧形波
;PID存在4种不同播散类型:喙-尾播散类型?侧方-内侧播散类型?尾-喙播散类型和对侧播散类型;Kir6.1基因敲除小鼠PID的发作次数(25.5 ± 6.5次)明显高于野生型小鼠(15.5 ± 4.8次)(P 0.05);Kir6.1基因敲除小鼠MCAO模型脑梗死体积百分比(38.2 ± 7.5)%明显大于野生型小鼠(27.8 ± 6.6)% (P < 0.05)?【结论】 四波长OIS成像技术可获得PID的高分辨率彩色影像
为更深入研究PID的时空特性创造了条件;Kir6.1基因敲除后促进PID的发作
可能与星形胶质细胞Kir6.1 KATP通道清除细胞外K+的能力下降有关;Kir6.1基因敲除后可能通过促进小鼠PID的发作
导致脑缺血损伤较野生型小鼠更为严重?
【Objective】 To study the optical intrinsic signal(OIS) imaging of peri-infarct depolarizations (PID) in mice and to investigate the influence of knockout of Kir6.1 on PID.【Methods】Kir6.1 knockout mice and wild type littermates were subjected to MCAO by standard intraluminal filament method. The main characteristics of PID were studied by 4-wavelength OIS imaging technique. 【Results】 PID were identified as consistent
red and blue interaction waves in cortical reflectance that slowly propagated peripherally from the origin site. There were 4 patterns of PID propagation including rostro-caudal
latero-medial
caudo-rostral
and contralateral pattern. Kir6.1 knockout mice had a mean of 25.5 ± 6.5 PID which was much higher than a mean of 15.5 ± 4.8 in wild type mice (P 0.05). Kir6.1 knockout mice showed an increased mean infarction volume (38.2 ± 7.5%) compared with wild type mice (27.8 ± 6.6%). 【Conclusion】 Using 4-wavelength OIS system
we are able to get high temporal-spatial resolution color images which are useful for analyzing temporal-spatial characteristics of PID in detail. Knockout of Kir6.1 facilitates induction of PID in focal cerebral ischemia
perhaps owing to decreasing spatial potassium buffering ability of astrocytes in kir6.1 knockout mice. Furthermore
more PID may contribute to the increased infarction volume in kir6.1 knockout mice.
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