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不稳定型心绞痛患者应用小剂量尿激酶前后内皮源性血管活性物质的变化(英文) 被引量:4

Changes of vasoactive substances originated endothelium on patients with unstable angina pectoris treated by low dose of urokinase
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摘要 目的分析不稳定型心绞痛患者应用小剂量尿激酶治疗前后内皮源性血管活性物质的变化,探讨小剂量尿激酶治疗心绞痛的机理。方法选择104例心电图负荷试验阳性、动态心电图出现缺血性改变的不稳定型心绞痛患者,于小剂量尿激酶治疗前后分别测定内皮素-1、组织型纤溶酶原激活物及其抑制剂的变化。结果小剂量尿激酶治疗后与治疗前相比较,组织型纤溶酶原激活物升高,内皮素-1及组织型纤溶酶原激活物抑制剂下降,其变化均具有显著性。结论小剂量尿激酶可明显调节不稳定型心绞痛患者常测定的内皮源性血管活性物质如内皮素-1、组织型纤溶酶原激活物及其抑制剂的活性,从而有效的治疗冠心病。 [Objective] To analyze the changes of vasoaetive substances originated endothelium in patients with unstable angina peetoris treated by low dose of urokinase and explore mechanisms of the drug to treat the unstable angina peetoris. [Methods] 104 patients of unstable angina peetoris were studied. Their ECG stress tests were abnormal and there were isehemic changes in Holter. Before and after urokinase treatments, endothelin-1, plasma tissue plasminogen activator and its inhibitor-lwere determined. [Results] Compared with pretreatments, after treatments,the activities of tissue plasminogen activator increased, endothelin-1 and the inhibitor-1 decreased. The changes were significant. [Conclusion] Low dose of urokinase can regulate the vasoactive substances originated endothelium obviously in patients with unstable angina pectoris. The major substances include endothelin-1, plasma tissue plasminogen activator and inhibitor-1. From this mechanism, urokinase can treat coronary heart disease effectively.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2005年第14期2092-2095,共4页 China Journal of Modern Medicine
关键词 心绞痛 尿激酶 内皮 血管活性物质 angina peetoris urokinase endothelium vasoaetive substances
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参考文献7

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  • 3Bare FW, Verheugt I, Col J, et al. Thrombolysis in patients with unstable angina improves the angiographic but not the chief con- trolled results of UNASEM, a multi-center randomized, placebo- controled, clinical trial with anistreplase [ J ]. Circulation,2012,82 (2) :131-137.
  • 4Juiben-Vague I, Alessic MC, Joly OP, et al. Plasma plasminogen activator inhibitor-1 in angina pectoris. Influence of plasma insu- lin and acute phase response [ J ]. Arteriosclerosis, 2009,9 ( 3 ) : 362-367.
  • 5Obenham J, Hendson HY, Wu TS, et al. Acute administration of Ginkgobi Ioba extract affords neuroprotection against permanent and transient focal cerebral ischemia in Sprague-Dawley rats[ J]. J Neurosci Res ,2009,68 (5) :656.
  • 6Timyer MB. Investigators effects of tissue plasminogen activator and- comparison of early invasive and conservative strategies in unstab- leangina and Non-Q-wave my ocardial infarction[ J ]. Trial Circula- tion,2010,89(3) :1545-1556.
  • 7Yanagisawa M, Kimura S, Fombe Y. A novel potent vasoconstric- tor peptide produced by vascular endothelial cells [ J ]. Nature, 2009,33(12) :411-416.
  • 8Tullio Palmerini,Diego Sangiorgi,Antonio Marzocchi,Corrado Tamburino,Imad Sheiban,Massimo Margheri,Giuseppe Vecchi,Giuseppe Sangiorgi,Nicoletta Franco,Antonio Bartorelli,Carlo Briguori,Luigi Vignali,Francesco Di Pede,Angelo Ramondo,Massimo Medda,Marco De Carlo,Leonardo Bolognese,Alberto Benassi,Cataldo Palmieri,Vincenzo Filippone,Giulia Lauria,Stefano De Servi.??Impact of Acute Coronary Syndromes on Two-Year Clinical Outcomes in Patients With Unprotected Left Main Coronary Artery Stenosis Treated With Drug-Eluting Stents(J)The American Journal of Cardiology . 2010 (2)
  • 9不稳定性心绞痛诊断和治疗建议(J)中国循环杂志. 2001(03)
  • 10刘国仗,胡大一,陶萍,诸骏仁,郭林妮,郭静萱,游凯.心血管药物临床试验评价方法的建议[J].中华心血管病杂志,1998,26(1):5-11. 被引量:1439

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