Electrophysiological and transcriptomic correlates of neuropathic pain in human dorsal root ganglion neurons

Robert Y. North(Baylor College of Medicine), Yan Li(The University of Texas MD Anderson Cancer Center), Pradipta Ray(The University of Texas at Dallas), Laurence D. Rhines(The University of Texas MD Anderson Cancer Center), Claudio E. Tatsui(The University of Texas MD Anderson Cancer Center), Ganesh Rao(The University of Texas MD Anderson Cancer Center), Caj A. Johansson(The University of Texas Health Science Center at Houston), Hongmei Zhang(The University of Texas MD Anderson Cancer Center), Yeun Hee Kim(The University of Texas at Dallas), Bo Zhang(The University of Texas at Dallas), Gregory Dussor(The University of Texas at Dallas), Tae Hoon Kim(The University of Texas at Dallas), Theodore J. Price(The University of Texas at Dallas), Patrick M. Dougherty(The University of Texas MD Anderson Cancer Center)
Brain
February 25, 2019
Cited by 297Open Access
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Abstract

Neuropathic pain encompasses a diverse array of clinical entities affecting 7-10% of the population, which is challenging to adequately treat. Several promising therapeutics derived from molecular discoveries in animal models of neuropathic pain have failed to translate following unsuccessful clinical trials suggesting the possibility of important cellular-level and molecular differences between animals and humans. Establishing the extent of potential differences between laboratory animals and humans, through direct study of human tissues and/or cells, is likely important in facilitating translation of preclinical discoveries to meaningful treatments. Patch-clamp electrophysiology and RNA-sequencing was performed on dorsal root ganglia taken from patients with variable presence of radicular/neuropathic pain. Findings establish that spontaneous action potential generation in dorsal root ganglion neurons is associated with radicular/neuropathic pain and radiographic nerve root compression. Transcriptome analysis suggests presence of sex-specific differences and reveals gene modules and signalling pathways in immune response and neuronal plasticity related to radicular/neuropathic pain that may suggest therapeutic avenues and that has the potential to predict neuropathic pain in future cohorts.


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