Overexpression of P2X3 and P2X7 receptors and TRPV1 channels in adrenomedullary Chromaffin cells in a rat model of neuropathic pain

We have tested the hypothesis that neuropathic pain acting as a stressor drives functional plasticity in the sympathoadrenal system. The relation between neuropathic pain and adrenal medulla function was studied with behavioral, immunohistochemical and electrophysiological techniques in rats subject...

Full description

Bibliographic Details
Authors: Arribas-Blázquez, Marina, Olivos-Oré, Luis Alcides, Barahona, María Victoria, Sánchez de la Muela, Mercedes, Solar Fernández, Virginia, Jiménez, Esperanza, Gualix, Javier, McIntosh, J. Michel, Ferrer-Montiel, Antonio, Miras-Portugal, María Teresa, Artalejo, Antonio R.
Format: article
Publication Date:2019
Country:España
Institution:Universidad Autónoma de Madrid
Repository:Biblos-e Archivo. Repositorio Institucional de la UAM
Language:English
OAI Identifier:oai:repositorio.uam.es:10486/691521
Online Access:http://hdl.handle.net/10486/691521
https://dx.doi.org/10.3390/ijms20010155
Access Level:Open access
Keyword:P2X3 receptors
P2X7 receptors
TRPV1 channels
α9 nicotinic acetylcholine receptors
Neuropathic pain
Chromaffin cells
Adrenal medulla
Stress
Medicina
Description
Summary:We have tested the hypothesis that neuropathic pain acting as a stressor drives functional plasticity in the sympathoadrenal system. The relation between neuropathic pain and adrenal medulla function was studied with behavioral, immunohistochemical and electrophysiological techniques in rats subjected to chronic constriction injury of the sciatic nerve. In slices of the adrenal gland from neuropathic animals, we have evidenced increased cholinergic innervation and spontaneous synaptic activity at the splanchnic nerve–chromaffin cell junction. Likewise, adrenomedullary chromaffin cells displayed enlarged acetylcholine-evoked currents with greater sensitivity to -conotoxin RgIA, a selective blocker of 9 subunit-containing nicotinic acetylcholine receptors, as well as increased exocytosis triggered by voltage-activated Ca2+ entry. Altogether, these adaptations are expected to facilitate catecholamine output into the bloodstream. Last, but most intriguing, functional and immunohistochemical data indicate that P2X3 and P2X7 purinergic receptors and transient receptor potential vanilloid-1 (TRPV1) channels are overexpressed in chromaffin cells from neuropathic animals. These latter observations are reminiscent of molecular changes characteristic of peripheral sensitization of nociceptors following the lesion of a peripheral nerve, and suggest that similar phenomena can occur in other tissues, potentially contributing to behavioral manifestations of neuropathic pain