Seyal M
Department of Neurology, University of California, Davis Medical Center, Sacramento 95817.
J Clin Neurophysiol. 1991 Jan;8(1):95-101. doi: 10.1097/00004691-199101000-00012.
The excitability cycles of the N1-P1-N2 waveforms of the scalp-recorded somatosensory evoked potential (SEP) and of the long-latency, cortical loop reflex electromyographic (EMG) activity were studied in two patients with cortical reflex myoclonus. Long-latency cortical loop reflex EMG activity in the thenar muscles and giant SEPs occurred following median nerve stimulation. The excitability cycle of the EMG paralleled that of the SEP. There was an initial period of attenuation of SEP and EMG amplitude at interstimulus intervals (ISIs) of less than 40 ms followed by a period of amplitude enhancement at an ISI of up to 200 ms followed by a second period of attenuation. The excitability cycle is abnormal and the SEP and EMG amplitude changes parallel each other. It is therefore likely that a common mechanism determines the abnormal excitability cycle. The substrate for this mechanism is unknown and may be diffuse or restricted. Oral 5-hydroxytryptophan (5-HTP) in therapeutic doses altered the SEP excitability cycle. 5-HTP did not attenuate the giant SEPs but did attenuate the long-latency reflex EMG. Therefore, 5-HTP's site of action may be different from the substrate underlying the mechanism that results in the giant SEPs. Additionally, spinal latency reflex EMG activity occurred following treatment with 5-HTP but was absent when the patient discontinued 5-HTP.
对两名皮质反射性肌阵挛患者的头皮记录体感诱发电位(SEP)的N1-P1-N2波形以及长潜伏期皮质环路反射肌电图(EMG)活动的兴奋性周期进行了研究。正中神经刺激后,大鱼际肌出现长潜伏期皮质环路反射EMG活动和巨大SEP。EMG的兴奋性周期与SEP的平行。在刺激间隔(ISI)小于40毫秒时,SEP和EMG振幅有一个初始衰减期,随后在ISI高达200毫秒时有一个振幅增强期,接着是第二个衰减期。兴奋性周期异常,SEP和EMG振幅变化相互平行。因此,很可能有一个共同机制决定了异常的兴奋性周期。该机制的底物尚不清楚,可能是弥漫性的或局限性的。治疗剂量的口服5-羟色氨酸(5-HTP)改变了SEP兴奋性周期。5-HTP没有减弱巨大SEP,但确实减弱了长潜伏期反射EMG。因此,5-HTP的作用部位可能与导致巨大SEP的机制所涉及的底物不同。此外,5-HTP治疗后出现了脊髓潜伏期反射EMG活动,但患者停用5-HTP时则消失。