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本文引用的文献

1
Collateral flow predicts response to endovascular therapy for acute ischemic stroke.侧支血流预测急性缺血性脑卒中血管内治疗的反应。
Stroke. 2011 Mar;42(3):693-9. doi: 10.1161/STROKEAHA.110.595256. Epub 2011 Jan 13.
2
Microbubbles improve sonothrombolysis in vitro and decrease hemorrhage in vivo in a rabbit stroke model.微泡增强兔卒中模型体外超声溶栓并减少体内出血。
Invest Radiol. 2011 Mar;46(3):202-7. doi: 10.1097/RLI.0b013e318200757a.
3
Ultrasound-accelerated thrombolysis in arterial and venous peripheral occlusions: fibrinogen level effects.超声辅助溶栓治疗动静脉周围血管闭塞:纤维蛋白原水平的影响。
J Vasc Interv Radiol. 2010 Aug;21(8):1165-72. doi: 10.1016/j.jvir.2010.03.020.
4
Stroke location and brain function in an embolic rabbit stroke model.栓塞性兔中风模型中的中风位置与脑功能。
J Vasc Interv Radiol. 2010 Jun;21(6):903-9. doi: 10.1016/j.jvir.2010.02.023. Epub 2010 Apr 22.
5
Therapeutic milestone: stroke declines from the second to the third leading organ- and disease-specific cause of death in the United States.治疗里程碑:在美国,中风从第二大器官特异性和疾病特异性死亡原因降至第三大。
Stroke. 2010 Mar;41(3):499-503. doi: 10.1161/STROKEAHA.109.571828. Epub 2010 Jan 14.
6
Inflammatory mechanisms in ischemic stroke: therapeutic approaches.缺血性脑卒中的炎症机制:治疗方法。
J Transl Med. 2009 Nov 17;7:97. doi: 10.1186/1479-5876-7-97.
7
US geographic distribution of rt-PA utilization by hospital for acute ischemic stroke.美国医院对急性缺血性中风使用重组组织型纤溶酶原激活剂(rt-PA)的地理分布情况。
Stroke. 2009 Nov;40(11):3580-4. doi: 10.1161/STROKEAHA.109.554626. Epub 2009 Oct 1.
8
Transcranial ultrasound in clinical sonothrombolysis (TUCSON) trial.经颅超声临床超声溶栓(TUCSON)试验
Ann Neurol. 2009 Jul;66(1):28-38. doi: 10.1002/ana.21723.
9
Microbubbles for thrombolysis of acute ischemic stroke.用于急性缺血性脑卒中溶栓的微泡
Cerebrovasc Dis. 2009;27 Suppl 2:55-65. doi: 10.1159/000203127. Epub 2009 Apr 16.
10
Thrombolysis with alteplase 3 to 4.5 hours after acute ischemic stroke.急性缺血性卒中发病3至4.5小时后使用阿替普酶进行溶栓治疗。
N Engl J Med. 2008 Sep 25;359(13):1317-29. doi: 10.1056/NEJMoa0804656.

成功的微泡超声溶栓,无需组织型纤溶酶原激活剂,在急性缺血性脑卒中兔模型中。

Successful microbubble sonothrombolysis without tissue-type plasminogen activator in a rabbit model of acute ischemic stroke.

机构信息

Department of Radiology, University of Arkansas for Medical Sciences, Little Rock, AR 72205-7199, USA.

出版信息

Stroke. 2011 Aug;42(8):2280-5. doi: 10.1161/STROKEAHA.110.607150. Epub 2011 Jun 23.

DOI:10.1161/STROKEAHA.110.607150
PMID:21700942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3266124/
Abstract

BACKGROUND AND PURPOSE

Microbubbles (MB) combined with ultrasound (US) have been shown to lyse clots without tissue-type plasminogen activator (tPA) both in vitro and in vivo. We evaluated sonothrombolysis with 3 types of MB using a rabbit embolic stroke model.

METHODS

New Zealand White rabbits (n=74) received internal carotid angiographic embolization of single 3-day-old cylindrical clots (0.6 × 4.0 mm). Groups included: (1) control (n=11) embolized without treatment; (2) tPA (n=20); (3) tPA+US (n=10); (4) perflutren lipid MB+US (n=16); (5) albumin 3 μm MB+US (n=8); and (6) tagged albumin 3 μm MB+US (n=9). Treatment began 1 hour postembolization. Ultrasound was pulsed-wave (1 MHz; 0.8 W/cm²) for 1 hour; rabbits with tPA received intravenous tPA (0.9 mg/kg) over 1 hour. Lipid MB dose was intravenous (0.16 mg/kg) over 30 minutes. Dosage of 3 μm MB was 5 × 10⁹ MB intravenously alone or tagged with eptifibatide and fibrin antibody over 30 minutes. Rabbits were euthanized at 24 hours. Infarct volume was determined using vital stains on brain sections. Hemorrhage was evaluated on hematoxylin and eosin sections.

RESULTS

Infarct volume percent was lower for rabbits treated with lipid MB+US (1.0%± 0.6%; P=0.013), 3 μm MB+US (0.7% ± 0.9%; P=0.018), and tagged 3 μm MB+US (0.8% ± 0.8%; P=0.019) compared with controls (3.5%± 0.8%). The 3 MB types collectively had lower infarct volumes (P=0.0043) than controls. Infarct volume averaged 2.2% ± 0.6% and 1.7%± 0.8% for rabbits treated with tPA alone and tPA+US, respectively (P=nonsignificant).

CONCLUSIONS

Sonothrombolysis without tPA using these MB is effective in decreasing infarct volumes. Study of human application and further MB technique development are justified.

摘要

背景与目的

微泡(MB)联合超声(US)已被证明可在体外和体内溶解无组织型纤溶酶原激活物(tPA)的血栓。我们使用兔栓塞性卒中模型评估了 3 种 MB 的超声溶栓作用。

方法

新西兰白兔(n=74)接受单枚 3 天龄圆柱形血栓(0.6×4.0mm)的颈内动脉血管造影栓塞。各组包括:(1)对照组(n=11),栓塞后不治疗;(2)tPA(n=20);(3)tPA+US(n=10);(4)perflutren 脂质 MB+US(n=16);(5)白蛋白 3μm MB+US(n=8);(6)标记白蛋白 3μm MB+US(n=9)。治疗于栓塞后 1 小时开始。超声为脉冲波(1MHz;0.8W/cm²),持续 1 小时;接受 tPA 的兔子在 1 小时内静脉注射 tPA(0.9mg/kg)。脂质 MB 剂量为 30 分钟内静脉注射(0.16mg/kg)。3μm MB 的剂量为 5×10⁹MB 静脉注射,单独或用依替巴肽和纤维蛋白抗体标记,30 分钟内完成。兔子在 24 小时时安乐死。脑切片用活体染料确定梗死体积。苏木精和伊红切片评估出血。

结果

脂质 MB+US(1.0%±0.6%;P=0.013)、3μm MB+US(0.7%±0.9%;P=0.018)和标记 3μm MB+US(0.8%±0.8%;P=0.019)治疗的兔子梗死体积百分比低于对照组(3.5%±0.8%)。与对照组相比,这 3 种 MB 类型的梗死体积总和更低(P=0.0043)。单独使用 tPA 和 tPA+US 治疗的兔子的梗死体积平均为 2.2%±0.6%和 1.7%±0.8%(P=无显著性差异)。

结论

无 tPA 的超声溶栓使用这些 MB 可有效降低梗死体积。有理由对其在人类中的应用和进一步的 MB 技术开发进行研究。