Advances in Neuroprotective Strategies: Potential Therapies for Intracerebral Hemorrhage

被引:110
作者
Hwang, Brian Y. [1 ]
Appelboom, Geoffrey [1 ]
Ayer, Amit [1 ]
Kellner, Christopher P. [1 ]
Kotchetkov, Ivan S. [1 ]
Gigante, Paul R. [1 ]
Haque, Raqeeb [1 ]
Kellner, Michael [1 ]
Connolly, E. Sander [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Neurol Inst New York, Dept Neurol Surg, New York, NY 10032 USA
关键词
Intracerebral hemorrhage; Pathophysiology; Neuroprotection; Secondary cerebral injury; mechanism; NECROSIS-FACTOR-ALPHA; BLOOD-BRAIN-BARRIER; TISSUE-PLASMINOGEN ACTIVATOR; NMDA RECEPTOR INHIBITION; ADENOSINE A(2A) RECEPTOR; N-TERMINAL KINASE; CELL-DEATH; MATRIX METALLOPROTEINASES; PERIHEMATOMAL EDEMA; TYROSINE PHOSPHORYLATION;
D O I
10.1159/000321870
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Intracerebral hemorrhage (ICH) is associated with higher mortality and morbidity than any other form of stroke. However, there currently are no treatments proven to improve outcomes after ICH, and therefore, new effective therapies are urgently needed. Growing insight into ICH pathophysiology has led to the development of neuroprotective strategies that aim to improve the outcome through reduction of secondary pathologic processes. Many neuroprotectants target molecules or pathways involved in hematoma degradation, inflammation or apoptosis, and have demonstrated potential clinical benefits in experimental settings. We extensively reviewed the current understanding of ICH pathophysiology as well as promising experimental neuroprotective agents with particular focus on their mechanisms of action. Continued advances in ICH knowledge, increased understanding of neuroprotective mechanisms, and improvement in the ability to modulate molecular and pathologic events with multitargeting agents will lead to successful clinical trials and bench-to-bedside translation of neuroprotective strategies. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:211 / 222
页数:12
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