PMID- 7823087 OWN - NLM STAT- MEDLINE DCOM- 19950210 LR - 20171213 IS - 0022-3077 (Print) IS - 0022-3077 (Linking) VI - 72 IP - 4 DP - 1994 Oct TI - Characteristics of somatotopic organization and spontaneous neuronal activity in the region of the thalamic principal sensory nucleus in patients with spinal cord transection. PG - 1570-87 AB - 1. We explored the region of the principal sensory nucleus of thalamus (Vc) during stereotactic surgical procedures for treatment of patients with pain after spinal cord transection (n = 23). Receptive fields (RFs) of thalamic single neurons and locations of sensations evoked by stimulation (projected field, PF) were determined by standard methods. The cellular thalamic region where sensations were evoked at < 25 microA was termed the "region of Vc." The region of Vc in spinal patients was subdivided into different areas according to RF and PF locations. Areas that were distant from the representation of the anesthetic part of the body were termed "spinal control" areas, whereas those that were adjacent to or included in the representation of the area of absolute sensory loss were termed "border zone/anesthetic" areas. The region of Vc in movement disorder patients were termed the "control" area. 2. Border zone/anesthetic areas of thalamus often exhibited increased representations of the border of the anesthetic part of the body in comparison with the representation of the same parts of the body in control and spinal control areas. 3. In control and spinal control areas the locations of RFs and PFs were usually well matched. However, in border zone/anesthetic areas of the thalamus there was frequently a mismatch between the location of RFs and PFs (RF/PF mismatch). In border zone/anesthetic areas, RFs were often located on the border of the anesthetic part of the body whereas PFs were referred to anesthetic parts of the body. 4. Analysis of first- and higher-order properties of spontaneous neuronal activity revealed that spike trains could be classified into two groups with distinct patterns of activity. The R group (n = 49) was characterized by independence of sequential interspike intervals (ISIs), a Poisson distribution of ISIs, initially inhibitory or flat autocovariance function (acvf), and low level of high-frequency bursting. The O group (n = 26) was characterized by correlation of sequential ISIs, large sustained postspike facilitation on the acvf, and high prevalence of high-frequency bursting--all consistent with a bursting pattern of activity. A third group of spike trains (n = 17) had an initially inhibitory or flat acvf and a unimodal, positively shifted, ISI distribution that did not meet criteria for a Poisson distribution. 5. Spike trains in the R group were much more common in control and control spinal areas, whereas those in the O group were more common in border zone/anesthetic areas.(ABSTRACT TRUNCATED AT 400 WORDS) FAU - Lenz, F A AU - Lenz FA AD - Department of Neurosurgery, Johns Hopkins University, Baltimore, Maryland 21287-7713. FAU - Kwan, H C AU - Kwan HC FAU - Martin, R AU - Martin R FAU - Tasker, R AU - Tasker R FAU - Richardson, R T AU - Richardson RT FAU - Dostrovsky, J O AU - Dostrovsky JO LA - eng GR - K08 NS-01384/NS/NINDS NIH HHS/United States GR - NS-28598/NS/NINDS NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Neurophysiol JT - Journal of neurophysiology JID - 0375404 RN - 0 (Calcium Channels) RN - SY7Q814VUP (Calcium) SB - IM MH - *Brain Mapping MH - Calcium/physiology MH - Calcium Channels/physiology MH - Electric Stimulation MH - Evoked Potentials/physiology MH - Humans MH - Movement Disorders/*physiopathology MH - Neural Pathways/physiology MH - Neurons/physiology MH - Nociceptors/*physiopathology MH - Paresthesia/physiopathology MH - Spinal Cord Injuries/*physiopathology MH - Synaptic Transmission/*physiology MH - Thalamic Nuclei/*physiopathology EDAT- 1994/10/01 00:00 MHDA- 1994/10/01 00:01 CRDT- 1994/10/01 00:00 PHST- 1994/10/01 00:00 [pubmed] PHST- 1994/10/01 00:01 [medline] PHST- 1994/10/01 00:00 [entrez] AID - 10.1152/jn.1994.72.4.1570 [doi] PST - ppublish SO - J Neurophysiol. 1994 Oct;72(4):1570-87. doi: 10.1152/jn.1994.72.4.1570.