» Articles » PMID: 35088129

Electrophysiological Characterization of Ectopic Spontaneous Discharge in Axotomized and Intact Fibers Upon Nerve Transection: a Role in Spontaneous Pain?

Overview
Journal Pflugers Arch
Specialty Physiology
Date 2022 Jan 28
PMID 35088129
Authors
Affiliations
Soon will be listed here.
Abstract

Many patients experience positive symptoms after traumatic nerve injury. Despite the increasing number of experimental studies in models of peripheral neuropathy and the knowledge acquired, most of these patients lack an effective treatment for their chronic pain. One possible explanation might be that most of the preclinical studies focused on the development of mechanical or thermal allodynia/hyperalgesia, neglecting that most of the patients with peripheral neuropathies complain mostly about spontaneous forms of pains. Here, we summarize the aberrant electrophysiological behavior of peripheral nerve fibers recorded in experimental models, the underlying pathophysiological mechanisms, and their relationship with the symptoms reported by patients. Upon nerve section, axotomized but also intact fibers develop ectopic spontaneous activity. Most interestingly, a proportion of axotomized fibers might present receptive fields in the skin far beyond the site of damage, indicative of a functional cross talk between neuromatose and intact fibers. All these features can be linked with some of the symptoms that neuropathic patients experience. Furthermore, we spotlight the consequence of primary afferents with different patterns of spontaneous discharge on the neural code and its relationship with chronic pain states. With this article, readers will be able to understand the pathophysiological mechanisms that might underlie some of the symptoms that experience neuropathic patients, with a special focus on spontaneous pain.

Citing Articles

Spinal neuromodulation using ultra low frequency waveform inhibits sensory signaling to the thalamus and preferentially reduces aberrant firing of thalamic neurons in a model of neuropathic pain.

Jones M, Matthews L, Lempka S, Verma N, Harris J, McMahon S Front Neurosci. 2025; 18:1512950.

PMID: 39897953 PMC: 11783389. DOI: 10.3389/fnins.2024.1512950.


The Intrinsic Neuronal Activation of the CXCR4 Signaling Axis Is Associated with a Pro-Regenerative State in Cervical Primary Sensory Neurons Conditioned by a Sciatic Nerve Lesion.

Dubovy P, Hradilova-Svizenska I, Brazda V, Jambrichova A, Svobodova V, Joukal M Int J Mol Sci. 2025; 26(1.

PMID: 39796050 PMC: 11720091. DOI: 10.3390/ijms26010193.


Human dorsal root ganglia are either preserved or completely lost after deafferentation by brachial plexus injury.

Sodmann A, Degenbeck J, Aue A, Schindehutte M, Schlott F, Arampatzi P Br J Anaesth. 2024; 133(6):1250-1262.

PMID: 39393999 PMC: 11589459. DOI: 10.1016/j.bja.2024.09.004.


Ultraconformable cuff implants for long-term bidirectional interfacing of peripheral nerves at sub-nerve resolutions.

Carnicer-Lombarte A, Boys A, Guemes A, Gurke J, Velasco-Bosom S, Hilton S Nat Commun. 2024; 15(1):7523.

PMID: 39214981 PMC: 11364531. DOI: 10.1038/s41467-024-51988-1.


Exaptation and Evolutionary Adaptation in Nociceptor Mechanisms Driving Persistent Pain.

Walters E Brain Behav Evol. 2023; 98(6):314-330.

PMID: 38035556 PMC: 10922759. DOI: 10.1159/000535552.


References
1.
Ackerley R, Watkins R . Microneurography as a tool to study the function of individual C-fiber afferents in humans: responses from nociceptors, thermoreceptors, and mechanoreceptors. J Neurophysiol. 2018; 120(6):2834-2846. DOI: 10.1152/jn.00109.2018. View

2.
ADRIAN E . The impulses produced by sensory nerve-endings: Part 4. Impulses from Pain Receptors. J Physiol. 1926; 62(1):33-51. PMC: 1514880. DOI: 10.1113/jphysiol.1926.sp002334. View

3.
Ali Z, Ringkamp M, Hartke T, Chien H, Flavahan N, Campbell J . Uninjured C-fiber nociceptors develop spontaneous activity and alpha-adrenergic sensitivity following L6 spinal nerve ligation in monkey. J Neurophysiol. 1999; 81(2):455-66. DOI: 10.1152/jn.1999.81.2.455. View

4.
Allodi I, Udina E, Navarro X . Specificity of peripheral nerve regeneration: interactions at the axon level. Prog Neurobiol. 2012; 98(1):16-37. DOI: 10.1016/j.pneurobio.2012.05.005. View

5.
Amir R, Devor M . Axonal cross-excitation in nerve-end neuromas: comparison of A- and C-fibers. J Neurophysiol. 1992; 68(4):1160-6. DOI: 10.1152/jn.1992.68.4.1160. View