A Novel Intervention for Cerebral Ischemia

脑缺血的新干预措施

• 批准号: 8974364
• 负责人: GUODONG CAO
• 金额: --
• 依托单位: VETERANS HEALTH ADMINISTRATION
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-04-01 至 2018-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8974364
• 关键词: Acute; Adult; Anabolism; Area; Blood - brain barrier anatomy; Blood capillaries; Brain; Brain Injuries; C57BL/6 Mouse; Cell Culture Techniques; Cell Death Induction; Cell Proliferation; Cerebral Ischemia; Cerebrum; Clinical; Drug Delivery Systems; Endothelial Cells; Fostering; Generations; Health; Human; Infarction; Intervention; Ischemia; Ischemic Brain Injury; Ischemic Stroke; Lead; Link; Middle Cerebral Artery Occlusion; Mission; Mus; Nerve; Neurologic; Neurological outcome; Neurons; Patient Care; Pharmaceutical Preparations; Physically Handicapped; Population; Production; Proteins; Quality of life; Recombinant Proteins; Recombinants; Recovery of Function; Reporting; Source; Stroke; Stroke prevention; System; Testing; Therapeutic; Therapeutic Agents; Transgenic Mice; Tube; Umbilical vein; United States; Veterans; Work; angiogenesis; brain repair; capillary; clinically relevant; disability; effective therapy; enzyme biosynthesis; functional improvement; functional outcomes; improved; in vivo; migration; neovascularization; nerve stem cell; neurogenesis; neurological recovery; neuronal replacement; neuroprotection; neurorestoration; neurovascular; nicotinamide phosphoribosyltransferase; novel; overexpression; post stroke; repaired; stroke rehabilitation; stroke survivor; success

DESCRIPTION (provided by applicant): Stroke is the leading cause of long-term disability in adults in the United States, and no therapy is available to prevent stroke-induced neurological deficits. Neurogenesis is one of the important endogenous mechanisms for neuronal replacement, repair and functional recovery after stroke. However, the majority of newly generated neurons in the brain die soon after stroke. Among the mechanisms that could foster viable neuronal replacement, a favorable neurovascular niche with proper angiogenesis and neovascularization is the most crucial one. Therefore, strategies to enhance both neurogenesis and angiogenesis would greatly improve neuronal replacement and neurological recovery after stroke. Nicotinamide phosphoribosyltransferase (NAMPT) has been proven to be neuroprotective against ischemic brain injury. NAMPT markedly promotes cell proliferation, migration and capillary-like tube formation in human umbilical vein endothelial cell cultures. However, the effect of NAMPT on angiogenesis in the context of cerebral ischemia is under-explored. Furthermore, whether NAMPT increases neurogenesis remains unknown. We have recently found that besides acute neuroprotection, NAMPT also promotes brain repair and neurovascular remodeling. Strikingly, we found that NAMPT recombinant protein can cross the blood brain barrier (BBB) and also improve long-term functional outcomes against cerebral ischemia. Therefore, the objective of this project is to test the novel neuroprotective/ neurorestorative function of NAMPT in the context of cerebral ischemia with a long-term aim to develop NAMPT as a novel, clinically relevant therapeutic agent for ischemic stroke. The hypothesis to be tested is that NAMPT protects against ischemic brain injury and improves long-term neurological outcomes by enhancing angiogenesis and neurogenesis. Focal ischemia will be induced in mice by middle cerebral artery occlusion (MCAO) to mimic the pathophysiological changes in the brain after clinical ischemic stroke. The following specific aims are proposed: Aim 1: Test the hypothesis that NAMPT reduces brain damage and improves long-term neurological outcomes after focal cerebral ischemia. The neuroprotective effect of NAMPT on ischemic brain injury will be first tested in transgenic mice that overexpress NAMPT specifically in the brain, and then its translational potential for the treatment of ischemic stroke will be furher tested using recombinant NAMPT protein. The endpoints for assessment include infarct size and functional outcomes. Aim 2: Test the hypothesis that NAMPT treatment enhances cerebral neurovascular remodeling, including augmented angiogenesis and neurogenesis after cerebral ischemia. The effect of recombinant NAMPT protein on post-stroke neovascularization in peri-infarct brain areas will be quantitatively analyzed. The effect of NAMPT on neural stem cell proliferation, migration, differentiation and neuronal replacement following ischemic stroke will also be examined. Relevance of the proposed work to the VA patient care mission Approximately 11,000 veterans are hospitalized annually with new strokes and up to 80,000 veterans are stroke survivors. The population with post-stroke physical disability continues to grow due to the lack of effective therapies to restrict and/or repair devastating neuronal damage after stroke. The proposed study will develop NAMPT as a novel, clinically feasible therapeutic strategy to offer acute neuroprotection as well as long-term neurological recovery after stroke. The success of this study will enhance post-stroke rehabilitation and improve quality of life for veterans suffering from stroke.

描述（由申请人提供）： 中风是美国成年人长期残疾的主要原因，目前尚无治疗方法可以预防中风引起的神经功能缺损。神经发生是脑卒中后神经元替代、修复和功能恢复的重要内源机制之一。然而，大脑中大多数新生成的神经元在中风后很快就会死亡。在可以促进可行的神经元替代的机制中，具有适当血管生成和新血管形成的有利神经血管生态位是最关键的机制。因此，增强神经发生和血管生成的策略将极大地改善中风后的神经元替代和神经功能恢复。 烟酰胺磷酸核糖转移酶 (NAMPT) 已被证明对缺血性脑损伤具有神经保护作用。 NAMPT显着促进人脐静脉内皮细胞增殖、迁移和毛细血管样管形成 细胞培养物。然而，NAMPT 对脑缺血背景下血管生成的影响尚未得到充分研究。此外，NAMPT 是否增加神经发生仍然未知。我们最近发现，除了急性神经保护之外，NAMPT还可以促进大脑修复和神经血管重塑。引人注目的是，我们发现 NAMPT 重组蛋白可以穿过血脑屏障 (BBB)，还可以改善脑缺血的长期功能结果。因此，该项目的目标是测试 NAMPT 在脑缺血背景下的新型神经保护/神经恢复功能，长期目标是将 NAMPT 开发为一种新型的、临床相关的缺血性中风治疗剂。待检验的假设是 NAMPT 可以防止缺血性脑损伤，并通过增强血管生成和神经发生来改善长期神经系统结果。通过大脑中动脉闭塞（MCAO）在小鼠中诱导局灶性缺血，以模拟临床缺血性中风后大脑的病理生理变化。提出以下具体目标： 目标 1：检验 NAMPT 减少局灶性脑缺血后脑损伤并改善长期神经系统结果的假设。 NAMPT 对缺血性脑损伤的神经保护作用将首先在大脑中特异性过度表达 NAMPT 的转基因小鼠中进行测试，然后使用重组 NAMPT 蛋白进一步测试其治疗缺血性中风的转化潜力。评估终点包括梗塞面积和功能结果。 目标 2：检验 NAMPT 治疗增强脑神经血管重塑的假设，包括增强脑缺血后的血管生成和神经发生。将定量分析重组 NAMPT 蛋白对中风后梗塞周围脑区新生血管形成的影响。还将检查 NAMPT 对缺血性中风后神经干细胞增殖、迁移、分化和神经元替代的影响。拟议工作与 VA 患者护理任务的相关性 每年约有 11,000 名退伍军人因新发中风住院，多达 80,000 名退伍军人是中风幸存者。由于缺乏有效的治疗方法来限制和/或修复中风后破坏性的神经元损伤，中风后身体残疾的人口持续增长。拟议的研究将开发 NAMPT 作为一种新颖的、临床上可行的治疗策略，以提供急性神经保护以及中风后的长期神经功能恢复。这项研究的成功将加强中风后康复并提高中风退伍军人的生活质量。