Dorsal root ganglion stimulation of injured sensory neurons in rats rapidly eliminates their spontaneous activity and relieves spontaneous pain
| Autor: | Guoliang Yu, Christina M Mecca, Michael S. Gold, Bin Pan, Ian Segel, Quinn H. Hogan, Dongman Chao |
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| Rok vydání: | 2021 |
| Předmět: |
Sensory Receptor Cells
business.industry Stimulation Nerve injury Sensory neuron Article Ganglion Rats Anesthesiology and Pain Medicine medicine.anatomical_structure Allodynia Spinal Nerves Neurology Dorsal root ganglion Hyperalgesia Ganglia Spinal Neuropathic pain medicine Animals Neuralgia Neurology (clinical) medicine.symptom business Neuroscience |
| Zdroj: | Pain |
| ISSN: | 1872-6623 |
| Popis: | Dorsal root ganglion field stimulation (GFS) relieves evoked and spontaneous neuropathic pain by use-dependent blockade of impulse trains through the sensory neuron T-junction, which becomes complete within less than 1 minute for C-type units, also with partial blockade of Aδ units. We used this tool in the spinal nerve ligation (SNL) rat model to selectively block sensory neuron spontaneous activity (SA) of axotomized neurons at the fifth lumbar (L5) level vs blockade of units at the L4 level that remain uninjured but exposed to inflammation. In vivo dorsal root single-unit recordings after SNL showed increased SA in L5 units but not L4 units. Ganglion field stimulation blocked this SA. Ganglion field stimulation delivered at the L5 dorsal root ganglion blocked mechanical hyperalgesia behavior, mechanical allodynia, and ongoing spontaneous pain indicated by conditioned place preference, whereas GFS at L4 blocked evoked pain behavior but not spontaneous pain. In vivo single-unit recordings of spinal cord dorsal horn (DH) wide-dynamic-range neurons showed elevated SA after SNL, which was reduced by GFS at the L5 level but not by GFS at the L4 level. In addition, L5 GFS, but not L4 GFS, increased mechanical threshold of DH units during cutaneous mechanical stimulation, while L5 GFS exceeded L4 GFS in reducing evoked firing rates. Our results indicate that SA in injured neurons supports increased firing of DH wide-dynamic-range neurons, contributing to hyperalgesia, allodynia, and ongoing pain. Ganglion field stimulation analgesic effects after nerve injury are at least partly attributable to blocking propagation of this SA. |
| Databáze: | OpenAIRE |
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