| Literature DB >> 2470573 |
Y T Hallström1, U Lindblom, B A Meyerson, T S Prevec.
Abstract
Spinal SEPs to electrical and mechanical stimulation of the upper limb of the non-painful side in 7 pain patients were recorded from the cervical epidural space. In response to electrical stimulation of the median nerve, the longitudinal distribution of the spinal postsynaptic negativity (N13) along the cord had a distinct level of maximal amplitude at the C5 vertebral body. When recorded at increasing distances cranial or caudal to this level, the latency of N13 was successively prolonged, in agreement with a spread-out near-field generator in the dorsal horn. Similar patterns of distribution and levels of maximal amplitude were demonstrated for the N13 wave evoked by electrical stimulation of the ulnar and thumb nerves as well as by mechanical stimulation of the thumb ball. The amplitude ratios of the N13 waves evoked by electrical stimulation of the median nerve and the thumb nerves, and by mechanical stimulation of the thumb ball were 3.9 to 1.4 to 1. The slow positive wave (P18), which has been assumed to represent recurrent presynaptic activity, had a somewhat different distribution, with a lower maximal amplitude and a less marked falling off in amplitude along the cord, as compared to the N13 component. The initial presynaptic positivity (P10) appeared with an almost constant amplitude along the cord. Tactile stimuli produced responses with considerably longer latency and duration than those obtained with electrical stimulation. There seemed to be a non-linear relationship between the amplitude of the response and the depth of skin indentation. The presented data contribute a more detailed picture of epidurally recorded spinal SEPs than previous studies. They will serve as a reference for further analysis of SEPs evoked by stimulation of the affected side in pain patients, to explore whether the painful state is associated with altered SEPs before or after therapeutic intervention.Entities:
Mesh:
Year: 1989 PMID: 2470573 DOI: 10.1016/0013-4694(89)90003-5
Source DB: PubMed Journal: Electroencephalogr Clin Neurophysiol ISSN: 0013-4694