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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Early insulin glycemic control combined with tPA thrombolysis reduces acute brain tissue damages in a focal embolic stroke model of diabetic rats
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Early insulin glycemic control combined with tPA thrombolysis reduces acute brain tissue damages in a focal embolic stroke model of diabetic rats

机译:在糖尿病大鼠局灶性栓塞性中风模型中,早期胰岛素血糖控制与tPA溶栓联合可减少急性脑组织损伤

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摘要

Background and Purpose-: Therapeutic effects of early insulin glycemic control for poststroke hyperglycemia in combination with tissue-type plasminogen activator (tPA) thrombolytic therapy have not yet been studied but are of great clinical interest. In this study, we tested the effects of insulin plus tPA combination in a model of focal embolic stroke in Type I diabetic rats. Methods-: Streptozotocin was used to produce Type I diabetes in male Wistar rats for 6 weeks and then embolic focal strokes were induced. All rats were treated with insulin or saline at 1 hour followed by tPA or saline at 1.5 hour after stroke. Mortality, infarction, hemispheric swelling, hemorrhagic transformation, and perfusion defects were examined at 24 hours after stroke. Total plasma plasminogen activator inhibitor-1 antigen and activity levels were measured before stroke and 1.5, 3, and 6 hours after stroke by ELISA. Results-: Early insulin glycemic control alone or tPA thrombolysis alone had no significant effects on ischemic infarction. However, early insulin glycemic control combined with tPA significantly reduced brain infarction and swelling, ameliorated tPA-associated hemorrhagic transformation, and improved plasma perfusion at 24 hours after stroke. We also found that the combination significantly decreased plasma plasminogen activator inhibitor-1 antigen level at 6 hours and plasminogen activator inhibitor-1 activity at 1.5 and 6 hours after stroke. Conclusions-: Early insulin glycemic control may be beneficial in combination with tPA thrombolysis for ischemic stroke with diabetes mellitus or poststroke hyperglycemia.
机译:背景与目的:早期胰岛素血糖控制对中风后高血糖与组织型纤溶酶原激活物(tPA)溶栓治疗的联合治疗尚未进行研究,但具有重要的临床意义。在这项研究中,我们在I型糖尿病大鼠局灶性栓塞性卒中模型中测试了胰岛素加tPA组合的作用。方法-:使用链脲佐菌素在雄性Wistar大鼠中产生I型糖尿病,持续6周,然后诱发栓塞性中风。所有大鼠在中风后1小时用胰岛素或生理盐水治疗,然后在中风后1.5小时用tPA或生理盐水治疗。脑卒中后24小时检查死亡率,梗死,半球肿胀,出血性转化和灌注缺陷。通过ELISA测量中风前和中风后1.5、3和6小时的总血浆纤溶酶原激活物抑制剂-1抗原和活性水平。结果-:早期单独进行胰岛素血糖控制或单独进行tPA溶栓对缺血性梗死无明显影响。但是,早期胰岛素血糖控制与tPA联合可显着减少脑梗塞和肿胀,改善tPA相关的出血性转化,并改善卒中后24小时的血浆灌注。我们还发现,该组合在卒中后6小时显着降低了血浆纤溶酶原激活物抑制剂1的抗原水平,并在中风后1.5和6小时降低了纤溶酶原激活物抑制剂1的活性。结论:早期胰岛素血糖控制可能与tPA溶栓联合治疗对糖尿病或中风后高血糖的缺血性卒中有益。

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