4.5 Article

LOCAL KNOCKDOWN OF THE NAV1.6 SODIUM CHANNEL REDUCES PAIN BEHAVIORS, SENSORY NEURON EXCITABILITY, AND SYMPATHETIC SPROUTING IN RAT MODELS OF NEUROPATHIC PAIN

Journal

NEUROSCIENCE
Volume 291, Issue -, Pages 317-330

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2015.02.010

Keywords

spontaneous activity; ectopic activity; Scn8a; sympathetic sprouting; allodynia; spinal nerve ligation

Categories

Funding

  1. NIH - United States [NS55860, NS45594]

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In the spinal nerve ligation (SNL) model of neuropathic pain, as in other pain models, abnormal spontaneous activity of myelinated sensory neurons occurs early and is essential for establishing pain behaviors and other pathologies. Sympathetic sprouting into the dorsal root ganglion (DRG) is observed after SNL, and sympathectomy reduces pain behavior. Sprouting and spontaneous activity may be mutually reinforcing: blocking neuronal activity reduces sympathetic sprouting, and sympathetic spouts functionally increase spontaneous activity in vitro. However, most studies in this field have used nonspecific methods to block spontaneous activity, methods that also block evoked and normal activity. In this study, we injected small inhibitory (si) RNA directed against the Na(V)1.6 sodium channel isoform into the DRG before SNL. This isoform can mediate high-frequency repetitive firing, like that seen in spontaneously active neurons. Local knockdown of Na(V)1.6 markedly reduced mechanical pain behaviors induced by SNL, reduced sympathetic sprouting into the ligated sensory ganglion, and blocked abnormal spontaneous activity and other measures of hyperexcitability in myelinated neurons in the ligated sensory ganglion. Immunohistochemical experiments showed that sympathetic sprouting preferentially targeted Na(V)1.6-positive neurons. Under these experimental conditions, Na(V)1.6 knockdown did not prevent or strongly alter single evoked action potentials, unlike previous less specific methods used to block spontaneous activity. Na(V)1.6 knockdown also reduced pain behaviors in another pain model, chronic constriction of the sciatic nerve, provided the model was modified so that the lesion site was relatively close to the siRNA-injected lumbar DRGs. The results highlight the relative importance of abnormal spontaneous activity in establishing both pain behaviors and sympathetic sprouting, and suggest that the Na(V)1.6 isoform may have value as a therapeutic target. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

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