A Novel Intervention for Cerebral Ischemia

脑缺血的新干预措施

• 批准号: 9912061
• 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 2019-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9912061
• 关键词: Acute; Adult; Anabolism; Area; Blood - brain barrier anatomy; Blood capillaries; Brain; Brain Infarction; Brain Injuries; C57BL/6 Mouse; Cell Culture Techniques; Cell Death Induction; Cell Proliferation; Cerebral Ischemia; Cerebrum; Clinical; Drug Delivery Systems; Endothelial Cells; Fostering; Generations; Human; Infarction; Intervention; Ischemia; Ischemic Brain Injury; Ischemic Stroke; Lead; Link; Middle Cerebral Artery Occlusion; Mission; Mus; Nerve; Nervous System Physiology; Neurologic Deficit; Neurologic Effect; 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; 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; public health relevance; 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，并且没有可用的治疗来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性机制之一。然而，大脑中大多数新产生的神经元在中风后很快死亡。在可能促进可行的神经元替代的机制中，具有适当的血管生成和新血管形成的有利的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大大改善卒中后神经元的替代和神经功能的恢复。 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对人脐静脉内皮细胞增殖、迁移及毛细血管样管形成的影响 细胞培养然而，NAMPT在脑缺血背景下对血管生成的影响尚未得到充分研究。此外，NAMPT是否会增加神经发生仍不清楚。我们最近发现，除了急性神经保护，NAMPT还促进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），并改善脑缺血的长期功能结局。因此，本项目的目的是测试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开发为缺血性卒中的新型临床相关治疗药物。待检验的假设是NAMPT通过增强血管生成和神经发生来防止缺血性脑损伤并改善长期神经学结果。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脑中的病理生理学变化。提出了以下具体目标：目标1：检验NAMPT减少脑损伤并改善局灶性脑缺血后长期神经功能结局的假设。NAMPT对缺血性脑损伤的神经保护作用将首先在脑中特异性过表达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卒中的翻译潜力。评估终点包括梗死面积和功能结局。 目标二：验证NAMPT治疗增强脑神经血管重塑的假设，包括脑缺血后血管生成和神经发生的增强。将定量分析重组NAMPT蛋白对梗死周围脑区域中卒中后新生血管形成的影响。还将检查NAMPT对缺血性卒中后神经干细胞增殖、迁移、分化和神经元替代的影响。拟议工作与退伍军人事务部患者护理使命的相关性每年约有11,000名退伍军人因新的中风住院，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，中风后肢体残疾的人群继续增长。这项拟议的研究将开发NAMPT作为一种新的，临床可行的治疗策略，以提供急性神经保护以及中风后的长期神经恢复。这项研究的成功将加强中风后康复，提高中风退伍军人的生活质量。

项目成果

Procalcitonin as a Biomarker for Malignant Cerebral Edema in Massive Cerebral Infarction.

促阳性蛋白作为大脑梗塞中恶性脑水肿的生物标志物。

• DOI: 10.1038/s41598-018-19267-4
• 发表时间: 2018-01-17
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Zhang Y;Liu G;Wang Y;Su Y;Leak RK;Cao G
• 通讯作者: Cao G

bFGF Protects Against Blood-Brain Barrier Damage Through Junction Protein Regulation via PI3K-Akt-Rac1 Pathway Following Traumatic Brain Injury.

BFGF在创伤性脑损伤后通过PI3K-AKT-RAC1途径来防止通过连接蛋白调节血脑屏障损伤。

• DOI: 10.1007/s12035-015-9583-6
• 发表时间: 2016-12
• 期刊: Molecular neurobiology
• 影响因子: 5.1
• 作者: Wang ZG;Cheng Y;Yu XC;Ye LB;Xia QH;Johnson NR;Wei X;Chen DQ;Cao G;Fu XB;Li XK;Zhang HY;Xiao J
• 通讯作者: Xiao J

Retinoic Acid Induced-Autophagic Flux Inhibits ER-Stress Dependent Apoptosis and Prevents Disruption of Blood-Spinal Cord Barrier after Spinal Cord Injury.

视黄酸诱导的自噬流抑制内质网应激依赖性细胞凋亡并防止脊髓损伤后血脊髓屏障的破坏

• DOI: 10.7150/ijbs.13229
• 发表时间: 2016
• 期刊: International journal of biological sciences
• 影响因子: 9.2
• 作者: Zhou Y;Zhang H;Zheng B;Ye L;Zhu S;Johnson NR;Wang Z;Wei X;Chen D;Cao G;Fu X;Li X;Xu HZ;Xiao J
• 通讯作者: Xiao J

(Z)-N-(2-Chloro-benzyl-idene)aniline N-oxide.

(Z)-N-(2-氯亚苄基)苯胺N-氧化物

• DOI: 10.1107/s1600536811015923
• 发表时间: 2011-06-01
• 期刊: Acta crystallographica. Section E, Structure reports online
• 作者: Fu Y;Liu Y;Yang Y;Chen Y
• 通讯作者: Chen Y

White matter injury in ischemic stroke.

• DOI: 10.1016/j.pneurobio.2016.04.005
• 发表时间: 2016-06
• 期刊: Progress in neurobiology
• 影响因子: 6.7
• 作者: Wang Y;Liu G;Hong D;Chen F;Ji X;Cao G
• 通讯作者: Cao G