de la Torre J C
Division of Neurosurgery, University of New Mexico, Albuquerque, USA.
Neurosurgery. 1995 Aug;37(2):273-9. doi: 10.1227/00006123-199508000-00012.
Mice were subjected to moderate (800 g/cm force) or severe (900 g/cm force) head injury and treated 5 minutes later with various compounds. Treatments consisted of intravenous administration of the following compounds: 1) fructose 1,6-diphosphate (FDP), 2) dimethyl sulfoxide (DMSO), 3) FDP + DMSO, and 4) vehicle nontreated. Sensory-motor evaluations 1 and 2 hours after 800 g/cm-force head injury showed that significant protection of motor function (grip test) was achieved with FDP + DMSO but not with treatment by either drug alone. Evaluation of mice following a severe 900-g/cm force injury demonstrated significant survival after treatment with FDP + DMSO but not with the vehicle or treatment by either of these agents alone. Histopathological morphometry indicated that cortical and hippocampal CA1 neurons were markedly protected from damage when mice were treated with combined FDP + DMSO. More modest protection of CA1 but not of cortical neurons was observed after treatment with DMSO alone but not after treatment with FDP alone or administration of the vehicle. These findings indicate that combining FDP with DMSO results in considerable synergy in protecting animals from sensory-motor loss and neuronal brain damage and in ultimate survival stemming from a moderate or severe closed head injury.
将小鼠置于中度(800 g/cm力)或重度(900 g/cm力)头部损伤模型中,并在5分钟后用各种化合物进行治疗。治疗包括静脉注射以下化合物:1)1,6-二磷酸果糖(FDP),2)二甲基亚砜(DMSO),3)FDP + DMSO,4)未处理的赋形剂。在800 g/cm力头部损伤后1小时和2小时进行的感觉运动评估显示,FDP + DMSO可显著保护运动功能(握力测试),但单独使用任何一种药物治疗均无此效果。对重度900 g/cm力损伤后的小鼠进行评估表明,FDP + DMSO治疗后小鼠存活率显著提高,而单独使用赋形剂或任何一种药物治疗均无此效果。组织病理学形态计量学表明,当小鼠接受FDP + DMSO联合治疗时,皮质和海马CA1神经元受到显著保护,免受损伤。单独使用DMSO治疗后,观察到CA1神经元有一定程度的保护,但皮质神经元没有,单独使用FDP治疗或给予赋形剂后则未观察到这种保护。这些发现表明,FDP与DMSO联合使用在保护动物免受感觉运动丧失和神经元脑损伤以及中度或重度闭合性头部损伤导致的最终存活方面具有显著的协同作用。