Nicotinamide Treatment in Traumatic Brain Injury: Operation Brain Trauma Therapy

被引:45
|
作者
Shear, Deborah A. [1 ]
Dixon, C. Edward [2 ]
Bramlett, Helen M. [3 ,4 ]
Mondello, Stefania [5 ]
Dietrich, W. Dalton [3 ]
Deng-Bryant, Ying [1 ]
Schmid, Kara E. [1 ]
Wang, Kevin K. W. [6 ]
Hayes, Ronald L. [7 ]
Povlishock, John T. [8 ]
Kochanek, Patrick M. [9 ]
Tortella, Frank C. [1 ]
机构
[1] Walter Reed Army Inst Res, Ctr Mil Psychiat & Neurosci, Brain Trauma Neuroprotect Neurorestorat, Silver Spring, MD USA
[2] Univ Pittsburgh, Sch Med, Brain Trauma Res Ctr, Dept Neurol Surg, Pittsburgh, PA 15260 USA
[3] Univ Miami, Miller Sch Med, Miami Project Cure Paralysis, Dept Neurol Surg, Miami, FL 33136 USA
[4] Vet Affairs Med Ctr, Bruce W Carter Dept, Miami, FL 33125 USA
[5] Univ Messina, Dept Neurosci, Messina, Italy
[6] Univ Florida, Dept Psychiat & Neurosci, Ctr Neuroprote & Biomarkers Res, Gainesville, FL USA
[7] Banyan Biomarkers Inc, Ctr Neuroprote & Biomarkers Res, Ctr Innovat Res, Alachua, FL USA
[8] Virginia Commonwealth Univ, Dept Anat & Neurobiol, Richmond, VA USA
[9] Univ Pittsburgh, Sch Med, Safar Ctr Resuscitat Res, Dept Crit Care Med, 3434 Fifth Ave, Pittsburgh, PA 15260 USA
关键词
therapy; fluid percussion; rat; biomarker; vitamin B; neuroprotection; penetrating ballistic-like brain injury; controlled cortical impact; FOCAL CEREBRAL-ISCHEMIA; IMPROVES FUNCTIONAL RECOVERY; CORTICAL CONTUSION INJURY; FLUID PERCUSSION INJURY; INFARCT VOLUME; WISTAR RATS; HYPOTHERMIA THERAPY; DELAYED TREATMENT; MODEL; PRECURSOR;
D O I
10.1089/neu.2015.4115
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Nicotinamide (vitamin B-3) 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.
引用
收藏
页码:523 / 537
页数:15
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