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21-氨基类固醇U74006F对小鼠实验性头部损伤的影响。

Effects of the 21-aminosteroid U74006F on experimental head injury in mice.

作者信息

Hall E D, Yonkers P A, McCall J M, Braughler J M

机构信息

CNS Diseases Research, Upjohn Company, Kalamazoo, Michigan.

出版信息

J Neurosurg. 1988 Mar;68(3):456-61. doi: 10.3171/jns.1988.68.3.0456.

DOI:10.3171/jns.1988.68.3.0456
PMID:3343616
Abstract

The ability of a novel non-glucocorticoid 21-aminosteroid U74006F to inhibit lipid peroxidation of central nervous system tissue in vitro and to enhance the early neurological recovery and survival of mice after a severe concussive head injury is described. In the in vitro studies, U74006F was found to be an extremely potent inhibitor of lipid peroxidation in an assay system where the glucocorticoid steroid methylprednisolone and the non-glucocortoid steroids U72099E and U75718A were almost completely ineffective. In the head-injury studies, unanesthetized male CF-1 mice were subjected to a 900 gm-cm closed head injury produced by a 50-gm weight being dropped 18 cm. This concussive injury resulted in immediate unconsciousness (loss of righting reflex) in all animals and death in approximately 30%. Survivors received a tail vein injection of either vehicle or U74006F (0.001 to 30 mg/kg) within 5 minutes postinjury. Their neurological status was evaluated 1 hour later using a grip test. The grip-test score indicated that intravenous administration of a single dose of U74006F resulted in a significant improvement by as much as 168.6% in the neurological status 1 hour postinjury over a broad dose range (0.003 to 30 mg/kg). A 1-mg/kg dose given intravenously within 5 minutes and again at 1 1/2 hours after a severe injury, in addition to improving early recovery, also increased the 1-week survival rate to 78.6% compared to 27.3% in vehicle-treated mice (p less than 0.02). The compound was also effective in enhancing early recovery after a more moderate injury. This study demonstrates that early treatment after severe concussive head injury with a potent inhibitor of iron-dependent lipid peroxidation can significantly benefit the injured brain in mice and promote both early neurological recovery and long-term survival.

摘要

本文描述了一种新型非糖皮质激素21-氨基类固醇U74006F在体外抑制中枢神经系统组织脂质过氧化的能力,以及在严重脑震荡性头部损伤后增强小鼠早期神经功能恢复和提高生存率的作用。在体外研究中,发现在一种检测系统中,U74006F是脂质过氧化的极强抑制剂,而糖皮质激素甲基强的松龙以及非糖皮质激素U72099E和U75718A几乎完全无效。在头部损伤研究中,未麻醉的雄性CF-1小鼠受到由50克重物从18厘米高处落下产生的900克厘米的闭合性头部损伤。这种震荡性损伤导致所有动物立即昏迷(翻正反射丧失),约30%的动物死亡。存活者在受伤后5分钟内通过尾静脉注射溶剂或U74006F(0.001至30毫克/千克)。1小时后使用握力测试评估它们的神经状态。握力测试评分表明,静脉注射单剂量U74006F在广泛的剂量范围(0.003至30毫克/千克)内,使受伤后1小时的神经状态显著改善高达168.6%。在严重损伤后5分钟内静脉注射1毫克/千克剂量,并在1个半小时后再次注射,除了改善早期恢复外,与溶剂处理的小鼠相比,还将1周生存率提高到78.6%,而溶剂处理小鼠的生存率为27.3%(p小于0.02)。该化合物在更中度损伤后增强早期恢复方面也有效。这项研究表明,严重脑震荡性头部损伤后用铁依赖性脂质过氧化的强效抑制剂进行早期治疗可使小鼠受伤的大脑显著受益,并促进早期神经功能恢复和长期生存。

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