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Painful peripheral nerve injury decreases calcium current in axotomized sensory neurons. Anesthesiology 2006 Jul;105(1):160-8

Date

07/01/2006

Pubmed ID

16810008

Pubmed Central ID

PMC3725035

DOI

10.1097/00000542-200607000-00026

Scopus ID

2-s2.0-33746874473 (requires institutional sign-in at Scopus site)   60 Citations

Abstract

BACKGROUND: Reports of Ca(2+) current I(Ca) loss after injury to peripheral sensory neurons do not discriminate between axotomized and spared neurons. The spinal nerve ligation model separates axotomized from spared neurons innervating the same site. The authors hypothesized that I(Ca) loss is a result of neuronal injury, so they compared axotomized L5 dorsal root ganglion neurons to spared L4 neurons, as well as neurons from rats undergoing skin incision alone.

METHODS: After behavioral testing, dissociated neurons from L4 and L5 dorsal root ganglia were studied in both current and voltage patch clamp modes. The biophysical consequence of I(Ca) loss on the action potential was confirmed using selective I(Ca) antagonists. Data were grouped into small, medium, and large cells for comparison.

RESULTS: Reduced I(Ca) was predominantly a consequence of axotomy (L5 after spinal nerve ligation) and was most evident in small and medium neurons. ICa losses were associated with action potential prolongation in small and medium cells, whereas the amplitude and duration of after hyperpolarization was reduced in medium and large neurons. Blockade with Ca(2+) channel antagonists showed that action potential prolongation and after hyperpolarization diminution were alike, attributable to the loss of I(Ca).

CONCLUSION: Axotomy is required for I(Ca) loss. I(Ca) loss correlated with changes in the biophysical properties of sensory neuron membranes during action potential generation, which were due to I(Ca) loss leading to decreased outward Ca(2+)-sensitive K currents. Taken together, these results suggest that neuropathic pain may be mediated, in part, by loss of I(Ca) and the cellular processes dependent on Ca(2+).

Author List

McCallum JB, Kwok WM, Sapunar D, Fuchs A, Hogan QH

Authors

Quinn H. Hogan MD Professor in the Anesthesiology department at Medical College of Wisconsin
Wai-Meng Kwok PhD Professor in the Anesthesiology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Action Potentials
Animals
Axotomy
Calcium
In Vitro Techniques
Male
Neurons, Afferent
Pain
Peripheral Nerve Injuries
Peripheral Nerves
Peripheral Nervous System Diseases
Rats
Rats, Sprague-Dawley