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氟桂利嗪和甲泼尼龙对实验性脊髓损伤后功能恢复的影响。

Effect of flunarizine and methylprednisolone on functional recovery after experimental spinal injury.

作者信息

De Ley G, Leybaert L

机构信息

Laboratorium voor Normale en Pathologische Fysiologie, Universiteit Gent, Belgium.

出版信息

J Neurotrauma. 1993 Spring;10(1):25-35. doi: 10.1089/neu.1993.10.25.

Abstract

The effect of flunarizine and methylprednisolone on the recovery of somatosensory evoked potentials (SEPs) was evaluated in an experimental model of spinal cord impact injury in anesthetized cats. In addition, the effect of flunarizine on posttraumatic spinal cord blood flow (SCBF) (using the hydrogen clearance technique) and interstitial calcium and potassium activity (ion-selective electrodes) was investigated. After the injury (600 g.cm), SEPs disappeared, followed by a spontaneous recovery to 17% of the preinjury amplitude at the end of the 4 h observation period. Flunarizine treatment (0.1 mg/kg IV, given 5 and 120 min after injury) resulted in a significantly improved recovery of SEPs, reaching 52% of the preinjury amplitude. Methylprednisolone treatment (30 mg/kg IV, given 5 min after injury) resulted in a 30% recovery level, significantly better than in untreated animals but significantly inferior to flunarizine treatment. Combination of both treatments resulted in a 62% recovery level, significantly better than after methylprednisolone treatment alone. Flunarizine treatment had no significant effect on the postinjury evolution of SCBF and interstitial potassium activity; it did, however, significantly accelerate the recovery of interstitial calcium activity, which sharply decreased immediately after injury. It is concluded that intravenous administration of the calcium entry blocker flunarizine improves the functional recovery of the spinal cord in the acute phase after experimental spinal impact injury. The observed improvement is not achieved by an effect on local blood flow but is possibly related to an inhibitory effect of the drug on cellular calcium entry.

摘要

在麻醉猫脊髓撞击伤的实验模型中,评估了氟桂利嗪和甲基强的松龙对体感诱发电位(SEP)恢复的影响。此外,还研究了氟桂利嗪对创伤后脊髓血流量(SCBF)(采用氢清除技术)以及间质钙和钾活性(离子选择性电极)的影响。损伤(600 g.cm)后,SEP消失,在4小时观察期结束时自发恢复至损伤前幅度的17%。氟桂利嗪治疗(0.1 mg/kg静脉注射,在损伤后5分钟和120分钟给予)使SEP的恢复显著改善,达到损伤前幅度的52%。甲基强的松龙治疗(30 mg/kg静脉注射,在损伤后5分钟给予)导致30%的恢复水平,明显优于未治疗的动物,但明显低于氟桂利嗪治疗。两种治疗联合导致62%的恢复水平,明显优于单独使用甲基强的松龙治疗后。氟桂利嗪治疗对损伤后SCBF和间质钾活性的演变没有显著影响;然而,它确实显著加速了间质钙活性的恢复,间质钙活性在损伤后立即急剧下降。结论是,静脉注射钙通道阻滞剂氟桂利嗪可改善实验性脊髓撞击伤急性期脊髓的功能恢复。观察到的改善不是通过对局部血流的影响实现的,而是可能与该药物对细胞钙内流的抑制作用有关。

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