Nantwi K D, El-Bohy A, Goshgarian H G
Department of Anatomy and Cell Biology, Wayne State University, School of Medicine, Detroit, Michigan 48201, USA.
Exp Neurol. 1996 Jul;140(1):53-9. doi: 10.1006/exnr.1996.0114.
This study assesses the effects of theophylline on enhancing phrenic nerve discharge and functional hemidiaphragmatic recovery after C2 spinal cord hemisection in adult female rats. There were three separate groups of spinal hemisected rats and one nonhemisected group studied. Twenty-four hours following C2 spinal hemisection, ipsilateral phrenic nerve activity was recorded under standardized, normoxic and then hypoxic conditions. After 30 min, theophylline was administered and the recordings were repeated in group 1 animals. In group 2, activity in both phrenic nerves was recorded simultaneously before and after drug administration. In a third group of rats, both ipsilateral phrenic nerve and hemidiaphragmatic activities were monitored before and after the drug. In control nonhemisected animals under standardized recording conditions, the effects of theophylline were quantitatively assessed by determining the mean area under integrated phrenic nerve discharge waveforms before and after drug administration. Generally, theophylline induced biphasic effects; i.e., at a low dose (15 mg/kg) it evoked excitation, while at a high dose (30 mg/kg) depression of respiratory activity predominated. In group 2 animals, respiratory activity was induced in the nerve ipsilateral to the hemisection and enhanced in the contralateral phrenic nerve for up to 3 h after a single standard dose of theophylline (15 mg/kg). Prior to drug administration, there was an absence of respiratory-related activity in both the phrenic nerve and hemidiaphragm ipsilateral to C2 spinal cord hemisection. A standard dose of theophylline, however, induced recovery of activity in both the phrenic nerve and the left hemidiaphragm ipsilateral to the hemisection in group 3 animals. In control (nonhemisected) animals, theophylline enhanced phrenic nerve activity, but decreased the duration of respiratory bursts. These results show for the first time that theophylline can activate latent respiratory motor pathways and thus restore the respiratory drive to phrenic motoneurons lost by spinal cord injury. Respiratory activity is not only reestablished in the phrenic nerve made quiescent by hemisection, but it is also enhanced in the contralateral phrenic nerve. The drug also restores function to the hemidiaphragm paralyzed by the spinal cord hemisection. The findings may have clinical relevance to human cases of cervical spinal cord injury in which respiratory function is compromised.
本研究评估了氨茶碱对成年雌性大鼠C2脊髓半横断后增强膈神经放电及半侧膈肌功能恢复的影响。研究中有三组单独的脊髓半横断大鼠和一组未横断大鼠。C2脊髓半横断后24小时,在标准化、常氧及随后的低氧条件下记录同侧膈神经活动。30分钟后,对第1组动物给予氨茶碱并重复记录。在第2组中,给药前后同时记录双侧膈神经活动。在第三组大鼠中,给药前后监测同侧膈神经和半侧膈肌活动。在标准化记录条件下的对照未横断动物中,通过测定给药前后膈神经放电综合波形下的平均面积,定量评估氨茶碱的作用。一般来说,氨茶碱产生双相效应;即低剂量(15mg/kg)时引起兴奋,而高剂量(30mg/kg)时呼吸活动抑制占主导。在第2组动物中,单次标准剂量氨茶碱(15mg/kg)后,半横断同侧神经诱导呼吸活动,对侧膈神经呼吸活动增强长达3小时。给药前,C2脊髓半横断同侧的膈神经和半侧膈肌均无呼吸相关活动。然而,标准剂量的氨茶碱在第3组动物中诱导了半横断同侧的膈神经和左半侧膈肌活动恢复。在对照(未横断)动物中,氨茶碱增强膈神经活动,但缩短呼吸爆发持续时间。这些结果首次表明,氨茶碱可激活潜在的呼吸运动通路,从而恢复因脊髓损伤而丧失的膈运动神经元的呼吸驱动。不仅在因半横断而静止的膈神经中重新建立了呼吸活动,而且对侧膈神经中的呼吸活动也增强了。该药物还使因脊髓半横断而麻痹的半侧膈肌恢复功能。这些发现可能与呼吸功能受损的人类颈脊髓损伤病例具有临床相关性。