Perceptual Correlates of Nociceptive Long-Term Potentiation and Long-Term Depression in Humans
Adult
Male
Pain Threshold
Analysis of Variance
Neuronal Plasticity
Long-Term Synaptic Depression
Long-Term Potentiation
Nociceptors
Pain
Neocortex
Middle Aged
Hippocampus
Sensitivity and Specificity
Electric Stimulation
Forearm
03 medical and health sciences
0302 clinical medicine
Conditioning, Psychological
Humans
Female
Pain Measurement
Skin
DOI:
10.1523/jneurosci.1222-03.2004
Publication Date:
2004-01-29T03:23:41Z
AUTHORS (5)
ABSTRACT
Long-term potentiation (LTP) and long-term depression (LTD) of synaptic strength are ubiquitous mechanisms of synaptic plasticity, but their functional relevance in humans remains obscure. Here we report that a long-term increase in perceived pain to electrical test stimuli was induced by high-frequency electrical stimulation (HFS) (5 × 1 sec at 100 Hz) of peptidergic cutaneous afferents (27% above baseline, undiminished for >3 hr). In contrast, a long-term decrease in perceived pain (27% below baseline, undiminished for 1 hr) was induced by low-frequency stimulation (LFS) (17 min at 1 Hz). Pain testing with punctate mechanical probes (200 μm diameter) in skin adjacent to the HFS–LFS conditioning skin site revealed a marked twofold to threefold increase in pain sensitivity (secondary hyperalgesia, undiminished for >3 hr) after HFS but also a moderate secondary hyperalgesia (30% above baseline) after strong LFS. Additionally, HFS but not LFS caused pain to light tactile stimuli in adjacent skin (allodynia). In summary, HFS and LFS stimulus protocols that induce LTP or LTD in spinal nociceptive pathways in animal experiments led to similar LTP- and LTD-like changes in human pain perception (long-term hyperalgesia or hypoalgesia) mediated by the conditioned pathway. Additionally, secondary hyperalgesia and allodynia in adjacent skin induced by the HFS protocol and, to a minor extent, also by the LFS protocol, suggested that these perceptual changes encompassed an LTP-like heterosynaptic facilitation of adjacent nociceptive pathways by a hitherto unknown mechanism.
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