Neuroprotection in acute stroke: targeting excitotoxicity, oxidative and nitrosative stress, and inflammation

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• 作者：Prof Á ; ngel Chamorro ; MD^a ; ^b ; ^{achamorro@clinic.ub.es" class="auth_mail" title="E-mail the corresponding author} ; Ulrich Dirnagl ; MD^c ; ^e ; Xabier Urra ; MD^a ; ^b ; Anna M Planas ; PhD^b ; ^d
• 刊名：Lancet Neurology
• 出版年：2016
• 出版时间：July 2016
• 年：2016
• 卷：15
• 期：8
• 页码：869-881
• 全文大小：649 K

文摘

Treatments for acute ischaemic stroke continue to evolve after the superior value of endovascular thrombectomy was confirmed over systemic thrombolysis. Unfortunately, numerous neuroprotective drugs have failed to show benefit in the treatment of acute ischaemic stroke, making the search for new treatments imperative. Increased awareness of the relevance of rigorous preclinical testing, and appropriate selection of study participants, might overcome the barriers to progress in stroke research. Relevant areas of interest include the search for safe and effective treatment strategies that combine neuroprotection reperfusion, better use of advanced brain imaging for patient selection, and wider implementation of prehospital conducted clinical trials. Randomised controlled trials of combination treatments completed within the past 5 years have included growth factors, hypothermia, minocycline, natalizumab, fingolimod, and uric acid; the latter two drugs with alteplase produced encouraging results. Blocking of excitotoxicity is also being reassessed in clinical trials with new approaches, such as the postsynaptic density-95 inhibitor NA-1, or peritoneal dialysis to remove excess glutamate. The findings of these randomised trials are anticipated to improve treatment options and clinical outcomes in of patients with acute stroke.