» Articles » PMID: 11007885

Changes in Expression of Two Tetrodotoxin-resistant Sodium Channels and Their Currents in Dorsal Root Ganglion Neurons After Sciatic Nerve Injury but Not Rhizotomy

Overview
Journal J Neurosci
Specialty Neurology
Date 2000 Sep 29
PMID 11007885
Citations 49
Authors
Affiliations
Soon will be listed here.
Abstract

Two TTX-resistant sodium channels, SNS and NaN, are preferentially expressed in c-type dorsal root ganglion (DRG) neurons and have been shown recently to have distinct electrophysiological signatures, SNS producing a slowly inactivating and NaN producing a persistent sodium current with a relatively hyperpolarized voltage-dependence. An attenuation of SNS and NaN transcripts has been demonstrated in small DRG neurons after transection of the sciatic nerve. However, it is not known whether changes in the currents associated with SNS and NaN or in the expression of SNS and NaN channel protein occur after axotomy of the peripheral projections of DRG neurons or whether similar changes occur after transection of the central (dorsal root) projections of DRG neurons. Peripheral and central projections of L4/5 DRG neurons in adult rats were axotomized by transection of the sciatic nerve and the L4 and L5 dorsal roots, respectively. DRG neurons were examined using immunocytochemical and patch-clamp methods 9-12 d after sciatic nerve or dorsal root lesion. Levels of SNS and NaN protein in the two types of injuries were paralleled by their respective TTX-resistant currents. There was a significant decrease in SNS and NaN signal intensity in small DRG neurons after peripheral, but not central, axotomy compared with control neurons. Likewise, there was a significant reduction in slowly inactivating and persistent TTX-resistant currents in these neurons after peripheral, but not central, axotomy compared with control neurons. These results indicate that peripheral, but not central, axotomy results in a reduction in expression of functional SNS and NaN channels in c-type DRG neurons and suggest a basis for the altered electrical properties that are observed after peripheral nerve injury.

Citing Articles

Ion Channel and Transporter Involvement in Chemotherapy-Induced Peripheral Neurotoxicity.

Pozzi E, Terribile G, Cherchi L, Di Girolamo S, Sancini G, Alberti P Int J Mol Sci. 2024; 25(12).

PMID: 38928257 PMC: 11203899. DOI: 10.3390/ijms25126552.


Ropivacaine Promotes Axon Regeneration by Regulating Nav1.8-mediated Macrophage Signaling after Sciatic Nerve Injury in Rats.

Cui Y, Wang X, Xu Y, Cao Y, Luo G, Zhao Z Anesthesiology. 2023; 139(6):782-800.

PMID: 37669448 PMC: 10723771. DOI: 10.1097/ALN.0000000000004761.


High-throughput combined voltage-clamp/current-clamp analysis of freshly isolated neurons.

Ghovanloo M, Tyagi S, Zhao P, Kiziltug E, Estacion M, Dib-Hajj S Cell Rep Methods. 2023; 3(1):100385.

PMID: 36814833 PMC: 9939380. DOI: 10.1016/j.crmeth.2022.100385.


Scorpion Neurotoxin Syb-prII-1 Exerts Analgesic Effect through Nav1.8 Channel and MAPKs Pathway.

Bai F, Song Y, Cao Y, Ban M, Zhang Z, Sun Y Int J Mol Sci. 2022; 23(13).

PMID: 35806068 PMC: 9266357. DOI: 10.3390/ijms23137065.


BmK DKK13, A Scorpion Toxin, Alleviates Pain Behavior in a Rat Model of Trigeminal Neuralgia by Modulating Voltage-Gated Sodium Channels and MAPKs/CREB Pathway.

Yang R, Song Y, Wang H, Chen C, Bai F, Li C Mol Neurobiol. 2022; 59(7):4535-4549.

PMID: 35579847 DOI: 10.1007/s12035-022-02855-x.


References
1.
Tonra J, Curtis R, Wong V, Cliffer K, Park J, Timmes A . Axotomy upregulates the anterograde transport and expression of brain-derived neurotrophic factor by sensory neurons. J Neurosci. 1998; 18(11):4374-83. PMC: 6792814. View

2.
Fjell J, Hjelmstrom P, Hormuzdiar W, Milenkovic M, Aglieco F, Tyrrell L . Localization of the tetrodotoxin-resistant sodium channel NaN in nociceptors. Neuroreport. 2000; 11(1):199-202. DOI: 10.1097/00001756-200001170-00039. View

3.
Reimer M, Kanje M . Peripheral but not central axotomy promotes axonal outgrowth and induces alterations in neuropeptide synthesis in the nodose ganglion of the rat. Eur J Neurosci. 1999; 11(10):3415-23. DOI: 10.1046/j.1460-9568.1999.00757.x. View

4.
Black J, Cummins T, Plumpton C, Chen Y, Hormuzdiar W, Clare J . Upregulation of a silent sodium channel after peripheral, but not central, nerve injury in DRG neurons. J Neurophysiol. 1999; 82(5):2776-85. DOI: 10.1152/jn.1999.82.5.2776. View

5.
Bisby M . Dependence of GAP43 (B50, F1) transport on axonal regeneration in rat dorsal root ganglion neurons. Brain Res. 1988; 458(1):157-61. DOI: 10.1016/0006-8993(88)90509-4. View