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新型神经血管保护剂:INV-155、INV-157、INV-159 和 INV-161 与硫辛酸和卡托普利在大鼠中风模型中的作用比较。

Novel Neurovascular Protective Agents: Effects of INV-155, INV-157, INV-159, and INV-161 versus Lipoic Acid and Captopril in a Rat Stroke Model.

机构信息

Department of Biomedical Sciences, University of Prince Edward Island, Charlottetown, PE, Canada C1A 4P3.

出版信息

Cardiol Res Pract. 2012;2012:319230. doi: 10.1155/2012/319230. Epub 2012 Jan 4.

DOI:10.1155/2012/319230
PMID:22263115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3259480/
Abstract

Background. Lipoic acid (LA), which has significant antioxidant properties, may also function as a potent neuroprotectant. The synthetic compounds INV-155, INV-157, INV-159, and INV-161 are physiochemical combinations of lipoic acid and captopril. We sought to determine if these compounds have neuroprotective potential following middle cerebral artery occlusion (MCAO) in rats. Methods. Male Sprague-Dawley rats were injected intravenously with captopril (1-50 mg/kg) 30 minutes prior to MCAO. Blood pressure, heart rate, baroreceptor reflex sensitivity, and infarct size were measured. In addition, dose response effect on infarct size and cardiovascular parameters was determined using INV-155, INV-157, INV-159, and INV-161 and compared to captopril and LA. Results. Pretreatment with captopril and LA at all doses tested was neuroprotective. The compounds INV-159 (0.5-10 mg/kg) and INV-161 (1-10 mg/kg) produced a significant,dose-dependent decrease in infarct size. In contrast, INV-155 and INV-157 had no effect on infarct size. Conclusions. Combined pretreatment with captopril potentiated the neuroprotective benefit observed following LA alone. Both INV-159 and INV-161 were also neuroprotective. These results suggest that patients taking combinations of captopril and LA, either as combination therapy or in the form of INV-159 or INV-161, may also benefit from significant protection against cerebral infarction.

摘要

背景

硫辛酸(LA)具有显著的抗氧化特性,也可能具有强大的神经保护作用。合成化合物 INV-155、INV-157、INV-159 和 INV-161 是硫辛酸和卡托普利的理化组合。我们试图确定这些化合物在大鼠大脑中动脉闭塞(MCAO)后是否具有神经保护潜力。

方法

雄性 Sprague-Dawley 大鼠在 MCAO 前 30 分钟静脉注射卡托普利(1-50mg/kg)。测量血压、心率、压力感受器反射敏感性和梗死面积。此外,使用 INV-155、INV-157、INV-159 和 INV-161 确定对梗死面积和心血管参数的剂量反应效应,并与卡托普利和 LA 进行比较。

结果

在所有测试剂量下,卡托普利和 LA 的预处理均具有神经保护作用。化合物 INV-159(0.5-10mg/kg)和 INV-161(1-10mg/kg)可显著降低梗死面积,呈剂量依赖性。相比之下,INV-155 和 INV-157 对梗死面积没有影响。

结论

卡托普利联合预处理增强了单独使用 LA 观察到的神经保护作用。INV-159 和 INV-161 也具有神经保护作用。这些结果表明,服用卡托普利和 LA 联合治疗的患者,无论是联合治疗还是以 INV-159 或 INV-161 的形式,也可能受益于对脑梗死的显著保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/88097df8a9ad/CRP2012-319230.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/fb9a6bd5ff9b/CRP2012-319230.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/d50ad299472a/CRP2012-319230.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/cbe3060255ed/CRP2012-319230.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/88097df8a9ad/CRP2012-319230.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/fb9a6bd5ff9b/CRP2012-319230.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/d50ad299472a/CRP2012-319230.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/cbe3060255ed/CRP2012-319230.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d224/3259480/88097df8a9ad/CRP2012-319230.004.jpg

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