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创伤性脑损伤中的烟酰胺治疗:脑创伤治疗行动

Nicotinamide Treatment in Traumatic Brain Injury: Operation Brain Trauma Therapy.

作者信息

Shear Deborah A, Dixon C Edward, Bramlett Helen M, Mondello Stefania, Dietrich W Dalton, Deng-Bryant Ying, Schmid Kara E, Wang Kevin K W, Hayes Ronald L, Povlishock John T, Kochanek Patrick M, Tortella Frank C

机构信息

1 Brain Trauma Neuroprotection/Neurorestoration, Center for Military Psychiatry and Neuroscience, Walter Reed Army Institute of Research , Silver Spring, Maryland.

2 Department of Neurological Surgery, Brain Trauma Research Center, University of Pittsburgh School of Medicine , Pittsburgh, Pennsylvania.

出版信息

J Neurotrauma. 2016 Mar 15;33(6):523-37. doi: 10.1089/neu.2015.4115.

Abstract

Nicotinamide (vitamin B3) was the first drug selected for cross-model testing by the Operation Brain Trauma Therapy (OBTT) consortium based on a compelling record of positive results in pre-clinical models of traumatic brain injury (TBI). Adult male Sprague-Dawley rats were exposed to either moderate fluid percussion injury (FPI), controlled cortical impact injury (CCI), or penetrating ballistic-like brain injury (PBBI). Nicotinamide (50 or 500 mg/kg) was delivered intravenously at 15 min and 24 h after injury with subsequent behavioral, biomarker, and histopathological outcome assessments. There was an intermediate effect on balance beam performance with the high (500 mg/kg) dose in the CCI model, but no significant therapeutic benefit was detected on any other motor task across the OBTT TBI models. There was an intermediate benefit on working memory with the high dose in the FPI model. A negative effect of the low (50 mg/kg) dose, however, was observed on cognitive outcome in the CCI model, and no cognitive improvement was observed in the PBBI model. Lesion volume analysis showed no treatment effects after either FPI or PBBI, but the high dose of nicotinamide resulted in significant tissue sparing in the CCI model. Biomarker assessments included measurements of glial fibrillary acidic protein (GFAP) and ubiquitin carboxyl-terminal hydrolase-1 (UCH-L1) in blood at 4 or 24 h after injury. Negative effects (both doses) were detected on biomarker levels of GFAP after FPI and on biomarker levels of UCH-L1 after PBBI. The high dose of nicotinamide, however, reduced GFAP levels after both PBBI and CCI. Overall, our results showed a surprising lack of benefit from the low dose nicotinamide. In contrast, and partly in keeping with the literature, some benefit was achieved with the high dose. The marginal benefits achieved with nicotinamide, however, which appeared sporadically across the TBI models, has reduced enthusiasm for further investigation by the OBTT Consortium.

摘要

烟酰胺(维生素B3)是创伤性脑损伤(TBI)临床前模型中首个基于令人信服的阳性结果记录被脑外伤治疗行动(OBTT)联盟选用于跨模型测试的药物。成年雄性Sprague-Dawley大鼠分别接受中度液压颅脑损伤(FPI)、控制性皮质撞击伤(CCI)或贯穿性弹道式脑损伤(PBBI)。烟酰胺(50或500mg/kg)在损伤后15分钟和24小时静脉给药,随后进行行为、生物标志物和组织病理学结果评估。在CCI模型中,高剂量(500mg/kg)对平衡木表现有中等程度影响,但在OBTT的TBI模型中的任何其他运动任务上均未检测到显著的治疗益处。在FPI模型中,高剂量对工作记忆有中等程度益处。然而,低剂量(50mg/kg)在CCI模型中对认知结果有负面影响,在PBBI模型中未观察到认知改善。损伤体积分析显示FPI或PBBI后均无治疗效果,但高剂量烟酰胺在CCI模型中导致显著的组织保护。生物标志物评估包括在损伤后4或24小时测量血液中的胶质纤维酸性蛋白(GFAP)和泛素羧基末端水解酶-1(UCH-L1)。FPI后GFAP生物标志物水平以及PBBI后UCH-L1生物标志物水平均检测到负面影响(两种剂量)。然而,高剂量烟酰胺在PBBI和CCI后均降低了GFAP水平。总体而言,我们的结果显示低剂量烟酰胺令人惊讶地缺乏益处。相比之下,部分与文献一致,高剂量取得了一些益处。然而,烟酰胺取得的边际益处,在TBI模型中偶尔出现,降低了OBTT联盟进一步研究的热情。

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