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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Threshold duration of ischemia for myogenic tone in middle cerebral arteries: effect on vascular smooth muscle actin.
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Threshold duration of ischemia for myogenic tone in middle cerebral arteries: effect on vascular smooth muscle actin.

机译:大脑中部动脉生肌张力缺血的阈值持续时间:对血管平滑肌肌动蛋白的影响。

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BACKGROUND AND PURPOSE: We investigated the effect of different periods of ischemia on the myogenic tone of middle cerebral arteries (MCAs) and tested the hypothesis that ischemia disrupts the actin cytoskeleton in vascular smooth muscle. METHODS: The MCA occlusion model was used in male Wistar rats (n=27) to induce different periods of ischemia (15, 30, and 120 minutes) with 24 hours of reperfusion. Successful occlusion was determined by laser-Doppler flowmetry. MCAs were then studied in vitro with a specialized arteriograph system that allowed control of transmural pressure and measurement of lumen diameter. After equilibration for 1 hour at transmural pressure of 75 mm Hg, lumen diameter was measured, and the amount of spontaneous myogenic tone was determined. Arteries were then fixed with 10% formalin while still pressurized in the arteriograph bath and stained for filamentous (F-) actin with fluorescently labeled phalloidin, a specific probe for F-actin. The amount of F-actin was quantified by confocal microscopy. RESULTS: The amount of tone was similar between control and 15 minutes of ischemia (27.0+/-2.0% and 25.3+/-1.7%, respectively; P>0.05) but was significantly diminished after 30 and 120 minutes (11.7+/-2.0% and 8.5+/-2.0%, respectively; P<0.01 versus control). F-actin content also decreased at the longer ischemic periods and correlated significantly with vascular tone (P=0.04) such that the lesser the tone, the lesser was the F-actin content. Fluorescence intensity for control and 15, 30, and 120 minutes of ischemia was (x10(7)) 3.21+/-0.25, 2.54+/-0.32 (P>0.05), 2.32+/-0.15 (P<0.01), and 2.22+/-0.16 (P<0.01), respectively. CONCLUSIONS: These results demonstrate that ischemia disrupts the actin cytoskeleton in smooth muscle and diminishes vascular tone of MCAs in a threshold-dependent manner. This effect likely exacerbates brain tissue damage during stroke, including infarction and edema formation.
机译:背景与目的:我们研究了缺血的不同时期对大脑中动脉(MCA)肌源性肌张力的影响,并验证了缺血会破坏血管平滑肌肌动蛋白细胞骨架的假设。方法:MCA闭塞模型用于雄性Wistar大鼠(n = 27),诱导不同时期的缺血(15、30和120分钟),再灌注24小时。通过激光多普勒血流仪确定成功的闭塞。然后使用专门的动脉造影系统对MCA进行体外研究,该系统可控制穿膜壁压力和测量管腔直径。在75mmHg的透壁压力下平衡1小时后,测量管腔直径,并测定自发肌原性肌张力。然后用10%福尔马林固定动脉,同时仍在动脉造影浴中加压,并用荧光标记的鬼笔环肽(F-肌动蛋白的特异性探针)对丝状(F-)肌动蛋白染色。通过共聚焦显微镜定量F-肌动蛋白的量。结果:对照组和缺血15分钟之间的紧张程度相似(分别为27.0 +/- 2.0%和25.3 +/- 1.7%; P> 0.05),但在30分钟和120分钟后(11.7 +/-)显着降低分别为2.0%和8.5 +/- 2.0%;与对照组相比,P <0.01)。 F-肌动蛋白含量在更长的缺血期也降低,并且与血管紧张度显着相关(P = 0.04),因此紧张程度越小,F-肌动蛋白含量越小。对照以及缺血15、30和120分钟的荧光强度为(x10(7))3.21 +/- 0.25、2.54 +/- 0.32(P> 0.05),2.32 +/- 0.15(P <0.01)和分别为2.22 +/- 0.16(P <0.01)。结论:这些结果表明缺血以阈值依赖性方式破坏了平滑肌中的肌动蛋白细胞骨架并降低了MCA的血管紧张度。这种作用可能加剧中风期间脑组织的损害,包括梗塞和水肿形成。

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