Feraboli-Lohnherr D, Barthe J Y, Orsal D
Laboratoire de Physiologie et Biologie de la Motricité, CNRS-URA 1448, Paris, France.
J Neurosci Res. 1999 Jan 1;55(1):87-98. doi: 10.1002/(SICI)1097-4547(19990101)55:1<87::AID-JNR10>3.0.CO;2-#.
The biogenic amine serotonin has been described in the literature as a powerful modulator of the spinal central pattern generator for locomotion. In the present study, we tested whether administration of serotonin or its agonist quipazine could restore motor activity in a model of paraplegia. One to three weeks after a complete transection of the spinal cord at a low thoracic level, rats were given either intrathecal injections of serotonin (5 mM, 15 microL) or intraperitoneal injections of quipazine (400-600 microg/kg). Both treatments allowed recovery of locomotor activity on a treadmill in response to tail pinching. As compared with the activity elicited before treatment, the locomotor activity produced by spinal animals was characterised by longer locomotor sequences with a larger number of successive steps, better body support, better interlimb coordination, and a higher amplitude of electromyographic bursts. These results suggest that serotonergic drugs could be used for the recovery of motor functions after lesions of the spinal cord.
生物胺血清素在文献中被描述为脊髓运动中枢模式发生器的强大调节剂。在本研究中,我们测试了给予血清素或其激动剂喹哌嗪是否能在截瘫模型中恢复运动活性。在胸段低位脊髓完全横断后1至3周,给大鼠鞘内注射血清素(5 mM,15 μL)或腹腔注射喹哌嗪(400 - 600 μg/kg)。两种治疗方法均能使大鼠在跑步机上对夹尾刺激产生运动活性恢复。与治疗前引发的活动相比,脊髓损伤动物产生的运动活性具有以下特点:运动序列更长,连续步数更多,身体支撑更好,肢体间协调性更好,肌电图爆发幅度更高。这些结果表明,血清素能药物可用于脊髓损伤后运动功能的恢复。