Variation in chronic nicotinamide treatment after traumatic brain injury can alter components of functional recovery independent of histological damage.
Variation in chronic nicotinamide treatment after traumatic brain injury can alter components of functional recovery independent of histological damage.
复制标题
DOI：
10.4161/oxim.1.1.6694
复制
发表时间：
2008-10
影响因子：
--
通讯作者：
Beare JE
中科院分区：
文献类型：
--
作者：
Hoane MR;Pierce JL;Kaufman NA;Beare JE
Previously, we have shown that the window of opportunity for nicotinamide (NAM) therapy (50 mg/kg) following cortical contusion injuries (CCI) extended to 4–8 hrs post-CCI when administered over a six day post-CCI interval. The purpose of the present study was to determine if a more chronic NAM treatment protocol administered following CCI would extend the current window of opportunity for effective treatment onset. Groups of rats received either unilateral CCI's or sham procedures. Initiation of NAM therapy (50 mg/kg, ip) began at either 15-min, 4-hrs, 8-hrs or 24-hrs post-injury. All groups received daily systemic treatments for 12 days post-CCI at 24 hr intervals. Behavioral assessments were conducted for 28 days post injury and included: vibrissae forelimb placing, bilateral tactile adhesive removal, forelimb asymmetry task and locomotor placing testing. Behavioral analysis on both the tactile removal and locomotor placing tests showed that all NAM-treated groups facilitated recovery of function compared to saline treatment. However, on the vibrissae-forelimb placing and forelimb asymmetry tests only the 4-hr and 8-hr NAM-treated groups were significantly different from the saline-treated group. The lesion analysis showed that treatment with NAM out to 8 hrs post-CCI significantly reduced the size of the injury cavity. The window of opportunity for NAM treatment is task-dependent and in some situations can extend to 24 hrs post-CCI. These results suggest that a long term treatment regimen of 50 mg/kg of NAM starting at the clinically relevant time points may prove efficacious in human TBI.
登录
查看更多内容
影响因子：
2.9
作者：
Hoane, Michael R.;Kaplan, Shelby A.;Ellis, Amy L.
通讯作者：
Ellis, Amy L.
影响因子：
2.7
作者：
BARTH, TM;JONES, TA;SCHALLERT, T
通讯作者：
SCHALLERT, T
影响因子：
15.9
作者：
COGGESHALL, RE
通讯作者：
COGGESHALL, RE
影响因子：
105.7
作者：
Dickinson, K;Bunn, F;Roberts, I
通讯作者：
Roberts, I
影响因子：
4.2
作者：
Strauss, KI;Barbe, MF;Narayan, RK
通讯作者：
Narayan, RK