Literature DB >> 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.

A A Sleeper1, T R Cummins, S D Dib-Hajj, W Hormuzdiar, L Tyrrell, S G Waxman, J A Black.   

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.

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Year:  2000        PMID: 11007885      PMCID: PMC6772759     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  63 in total

1.  Rescue of alpha-SNS sodium channel expression in small dorsal root ganglion neurons after axotomy by nerve growth factor in vivo.

Authors:  S D Dib-Hajj; J A Black; T R Cummins; A M Kenney; J D Kocsis; S G Waxman
Journal:  J Neurophysiol       Date:  1998-05       Impact factor: 2.714

2.  Localization of the tetrodotoxin-resistant sodium channel NaN in nociceptors.

Authors:  J Fjell; P Hjelmström; W Hormuzdiar; M Milenkovic; F Aglieco; L Tyrrell; S Dib-Hajj; S G Waxman; J A Black
Journal:  Neuroreport       Date:  2000-01-17       Impact factor: 1.837

3.  Dependence of GAP43 (B50, F1) transport on axonal regeneration in rat dorsal root ganglion neurons.

Authors:  M A Bisby
Journal:  Brain Res       Date:  1988-08-16       Impact factor: 3.252

4.  Axotomy upregulates the anterograde transport and expression of brain-derived neurotrophic factor by sensory neurons.

Authors:  J R Tonra; R Curtis; V Wong; K D Cliffer; J S Park; A Timmes; T Nguyen; R M Lindsay; A Acheson; P S DiStefano
Journal:  J Neurosci       Date:  1998-06-01       Impact factor: 6.167

5.  Injury-associated induction of GAP-43 expression displays axon branch specificity in rat dorsal root ganglion neurons.

Authors:  D J Schreyer; J H Skene
Journal:  J Neurobiol       Date:  1993-07

6.  Peripheral but not central axotomy promotes axonal outgrowth and induces alterations in neuropeptide synthesis in the nodose ganglion of the rat.

Authors:  M Reimer; M Kanje
Journal:  Eur J Neurosci       Date:  1999-10       Impact factor: 3.386

7.  Upregulation of a silent sodium channel after peripheral, but not central, nerve injury in DRG neurons.

Authors:  J A Black; T R Cummins; C Plumpton; Y H Chen; W Hormuzdiar; J J Clare; S G Waxman
Journal:  J Neurophysiol       Date:  1999-11       Impact factor: 2.714

8.  Axotomy increases the excitability of dorsal root ganglion cells with unmyelinated axons.

Authors:  J M Zhang; D F Donnelly; X J Song; R H Lamotte
Journal:  J Neurophysiol       Date:  1997-11       Impact factor: 2.714

9.  Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH.

Authors:  F Lehmann-Horn; G Küther; K Ricker; P Grafe; K Ballanyi; R Rüdel
Journal:  Muscle Nerve       Date:  1987-05       Impact factor: 3.217

10.  NaN, a novel voltage-gated Na channel, is expressed preferentially in peripheral sensory neurons and down-regulated after axotomy.

Authors:  S D Dib-Hajj; L Tyrrell; J A Black; S G Waxman
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-21       Impact factor: 11.205

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  43 in total

1.  Glycosylation alters steady-state inactivation of sodium channel Nav1.9/NaN in dorsal root ganglion neurons and is developmentally regulated.

Authors:  L Tyrrell; M Renganathan; S D Dib-Hajj; S G Waxman
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

2.  En masse in vitro functional profiling of the axonal mechanosensitivity of sensory neurons.

Authors:  Dmitry Usoskin; Misha Zilberter; Sten Linnarsson; Jens Hjerling-Leffler; Per Uhlén; Tibor Harkany; Patrik Ernfors
Journal:  Proc Natl Acad Sci U S A       Date:  2010-08-24       Impact factor: 11.205

3.  A single sodium channel mutation produces hyper- or hypoexcitability in different types of neurons.

Authors:  Anthony M Rush; Sulayman D Dib-Hajj; Shujun Liu; Theodore R Cummins; Joel A Black; Stephen G Waxman
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-15       Impact factor: 11.205

4.  Depolarization and electrical stimulation enhance in vitro and in vivo sensory axon growth after spinal cord injury.

Authors:  Ioana Goganau; Beatrice Sandner; Norbert Weidner; Karim Fouad; Armin Blesch
Journal:  Exp Neurol       Date:  2017-11-26       Impact factor: 5.330

5.  TREK2 expressed selectively in IB4-binding C-fiber nociceptors hyperpolarizes their membrane potentials and limits spontaneous pain.

Authors:  Cristian Acosta; Laiche Djouhri; Roger Watkins; Carol Berry; Kirsty Bromage; Sally N Lawson
Journal:  J Neurosci       Date:  2014-01-22       Impact factor: 6.167

Review 6.  Sodium channels and pain: from toxins to therapies.

Authors:  Fernanda C Cardoso; Richard J Lewis
Journal:  Br J Pharmacol       Date:  2017-09-02       Impact factor: 8.739

7.  Nerve injury increases brain-derived neurotrophic factor levels to suppress BK channel activity in primary sensory neurons.

Authors:  Xue-Hong Cao; Shao-Rui Chen; Li Li; Hui-Lin Pan
Journal:  J Neurochem       Date:  2012-04-12       Impact factor: 5.372

8.  Glial-derived neurotrophic factor upregulates expression of functional SNS and NaN sodium channels and their currents in axotomized dorsal root ganglion neurons.

Authors:  T R Cummins; J A Black; S D Dib-Hajj; S G Waxman
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

9.  Bilateral downregulation of Nav1.8 in dorsal root ganglia of rats with bone cancer pain induced by inoculation with Walker 256 breast tumor cells.

Authors:  Xue-Rong Miao; Xiao-Fei Gao; Jing-Xiang Wu; Zhi-Jie Lu; Zhang-Xiang Huang; Xiao-Qing Li; Cheng He; Wei-Feng Yu
Journal:  BMC Cancer       Date:  2010-05-20       Impact factor: 4.430

10.  Blockade of Nav1.8 currents in nociceptive trigeminal neurons contributes to anti-trigeminovascular nociceptive effect of amitriptyline.

Authors:  Jingyao Liang; Xiaoyan Liu; Meiyan Pan; Wei Dai; Zhao Dong; Xiaolin Wang; Ruozhuo Liu; Jianquan Zheng; Shengyuan Yu
Journal:  Neuromolecular Med       Date:  2013-11-30       Impact factor: 3.843

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