The effects of capsaicin applied to peripheral nerves on responses of a group of lamina I cells in adult rats
- 9 August 1984
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 227 (3) , 393-400
- https://doi.org/10.1002/cne.902270309
Abstract
In adult rats, the sciatic and saphenous nerves on one side were treated topically with capsaicin. The capsaicin treatment had the effect of increasing the latency for withdrawal of the foot from hot water; 11–22 days later, the animals were decerebrated, and cells in the superficial dorsal horn of the lumbar cord with axons projecting in the contralateral dorsolateral funiculus (DLF) were examined electrophysiologically on the treated and untreated sides of the cord. HRP was applied to cut axons of the DLF at C4, in other rats, and retrograde labelling of cells in the lumbar cord indicated that most or all of the recordings in the capsaicin‐treated animals were likely to originate from lamina 1. The dorsal horn cells, with receptive fields on the foot, showed decreased responses to electrically evoked afferent impulses in C fibres and grossly altered receptive fields. After capsaicin treatment, the proportion of cells responding to C afferents fell from 83% to 14%. The proportion responding only to C afferents and not to A afferents fell from 9% to 0%. The receptive fields (RFs) of these cells showed two gross abnormalities; 32% of the cells on the treated side had no apparent RF or an ill‐defined, intermittent RF, whereas such cells were rare on the untreated side or in intact animals. By contrast 49% of the cells had grossly expanded RFs with an average area of 430 mm2 against the normal average size of 130 mm2. The antidromic conduction velocity of the axons of the cells was measured, and while there was no significant change in the number of cells with axons conducting above 3 m/second, an increased number of cells with lower velocities were recorded. It is suggested that the capsaicin treatment induced dendritic changes in cells with small axons allowing antidromic spikes to invade these cells.Keywords
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