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免疫系统在脑卒中治疗新方法中的意义。

Implications of immune system in stroke for novel therapeutic approaches.

机构信息

Department of Molecular Pharmacology and Physiology, School of Basic Biomedical Sciences, College of Medicine, University of South Florida, MDC Box 9, 12901, Bruce B Downs Blvd., Tampa, FL, 33612, USA.

出版信息

Transl Stroke Res. 2010 Jun;1(2):85-95. doi: 10.1007/s12975-009-0003-y. Epub 2010 Jan 13.

DOI:10.1007/s12975-009-0003-y
PMID:24323491
Abstract

Each year, approximately 795,000 people suffer a new or recurrent stroke. About 610,000 of these are first attacks, and 185,000 are recurrent attacks. Currently, the only FDA approved treatment for ischemic stroke is the thrombolytic recombinant tissue plasminogen activator (Alteplase), which must be given within 4.5 h of stroke onset. Beyond this time, apoptotic and inflammatory processes greatly diminish the therapeutic benefits of current treatments. While there have been many experimental treatments for stroke that showed promising preclinical efficacy, these treatments have failed to show efficacy in clinical trials. In many of these cases, the preclinical animal studies did not model the clinical setting effectively. The injury that occurs following stroke is a dynamic process. To effectively treat stroke patients at clinically relevant timepoints, it is imperative to understand both the humeral and cell-mediated phenomena that occur throughout the body in response to ischemic injury over time. Promising experimental therapeutics designed to be given 1 to 2 days following stroke require both neuroprotective and anti-inflammatory properties in order to be efficacious.

摘要

每年,约有 795,000 人遭受新的或复发的中风。其中约有 610,000 人是首次发作,185,000 人是复发发作。目前,唯一获得 FDA 批准用于缺血性中风的治疗方法是溶栓重组组织纤溶酶原激活剂(阿替普酶),必须在中风发作后 4.5 小时内给予。超过这个时间,细胞凋亡和炎症过程会大大降低现有治疗方法的疗效。尽管有许多针对中风的实验治疗方法显示出有希望的临床前疗效,但这些治疗方法在临床试验中未能显示出疗效。在许多情况下,临床前动物研究没有有效地模拟临床环境。中风后发生的损伤是一个动态过程。为了在临床上相关的时间点有效地治疗中风患者,必须了解随着时间的推移,身体对缺血性损伤的反应中发生的全身和细胞介导的现象。旨在中风后 1 至 2 天内给予的有前途的实验治疗方法,为了有效,需要具有神经保护和抗炎特性。

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Blockade of adrenoreceptors inhibits the splenic response to stroke.肾上腺素能受体的阻断抑制脾脏对中风的反应。
Exp Neurol. 2009 Jul;218(1):47-55. doi: 10.1016/j.expneurol.2009.03.044. Epub 2009 Apr 14.
2
The hallucinogen N,N-dimethyltryptamine (DMT) is an endogenous sigma-1 receptor regulator.致幻剂N,N-二甲基色胺(DMT)是一种内源性σ-1受体调节剂。
Science. 2009 Feb 13;323(5916):934-7. doi: 10.1126/science.1166127.
3
Microglia protect neurons against ischemia by synthesis of tumor necrosis factor.小胶质细胞通过合成肿瘤坏死因子来保护神经元免受缺血损伤。
J Neurosci. 2009 Feb 4;29(5):1319-30. doi: 10.1523/JNEUROSCI.5505-08.2009.
4
Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee.《2009年心脏病和中风统计数据更新:美国心脏协会统计委员会及中风统计小组委员会报告》
Circulation. 2009 Jan 27;119(3):480-6. doi: 10.1161/CIRCULATIONAHA.108.191259.
5
sigma-1 receptor modulation of acid-sensing ion channel a (ASIC1a) and ASIC1a-induced Ca2+ influx in rat cortical neurons.大鼠皮层神经元中σ-1受体对酸敏感离子通道a(ASIC1a)及ASIC1a诱导的Ca2+内流的调节
J Pharmacol Exp Ther. 2008 Nov;327(2):491-502. doi: 10.1124/jpet.108.143974. Epub 2008 Aug 22.
6
Stroke-induced immunodepression and post-stroke infections: lessons from the preventive antibacterial therapy in stroke trial.中风诱导的免疫抑制与中风后感染:中风预防性抗菌治疗试验的经验教训
Neuroscience. 2009 Feb 6;158(3):1184-93. doi: 10.1016/j.neuroscience.2008.07.044. Epub 2008 Aug 5.
7
Lacunar infarcts: no black holes in the brain are benign.腔隙性梗死:大脑中没有黑洞是良性的。 (此译文似乎不太符合正常逻辑表达,原文表述可能有误,推测正确原文可能是“Lacunar infarcts: no black holes in the brain are malignant.”,若如此,译文为“腔隙性梗死:大脑中的黑洞并非都是恶性的。” )
Pract Neurol. 2008 Aug;8(4):222-8. doi: 10.1136/jnnp.2008.153601.
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Harms and benefits of lymphocyte subpopulations in patients with acute stroke.急性中风患者淋巴细胞亚群的危害与益处
Neuroscience. 2009 Feb 6;158(3):1174-83. doi: 10.1016/j.neuroscience.2008.06.014. Epub 2008 Jun 13.
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Trends in incidence, risk factors, and survival in symptomatic lacunar stroke in Dijon, France, from 1989 to 2006: a population-based study.1989年至2006年法国第戎有症状腔隙性卒中的发病率、危险因素及生存率趋势:一项基于人群的研究。
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