Literature DB >> 9169448

A novel tetrodotoxin-sensitive, voltage-gated sodium channel expressed in rat and human dorsal root ganglia.

L Sangameswaran1, L M Fish, B D Koch, D K Rabert, S G Delgado, M Ilnicka, L B Jakeman, S Novakovic, K Wong, P Sze, E Tzoumaka, G R Stewart, R C Herman, H Chan, R M Eglen, J C Hunter.   

Abstract

Dorsal root ganglion neurons express a wide repertoire of sodium channels with different properties. Here, we report the cloning from rat, dorsal root ganglia (DRG), cellular expression, and functional analysis of a novel tetrodotoxin-sensitive peripheral sodium channel (PN), PN1. PN1 mRNA is expressed in many different tissues. Within the rat DRG, both the mRNA and PN1-like immunoreactivity are present in small and large neurons. The abundance of sodium channel mRNAs in rat DRG is rBI > PN1 >/= PN3 >>> rBIII by quantitative reverse transcription-polymerase chain reaction analysis. Data from reverse transcription-polymerase chain reaction and sequence analyses of human DRG and other human tissues suggest that rat PN1 is an ortholog of the human neuroendocrine channel. In Xenopus oocytes, PN1 exhibits kinetics that are similar to rBIIa sodium currents and is inhibited by tetrodotoxin with an IC50 of 4.3 +/- 0.92 nM. Unlike rBIIa, the inactivation kinetics of PN1 are not accelerated by the coexpression of the beta-subunits.

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Year:  1997        PMID: 9169448     DOI: 10.1074/jbc.272.23.14805

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  86 in total

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8.  Electrophysiological properties of sodium current subtypes in small cells from adult rat dorsal root ganglia.

Authors:  A M Rush; M E Bräu; A A Elliott; J R Elliott
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9.  The sodium channel blocker RS100642 reverses down-regulation of the sodium channel alpha-subunit Na(v) 1.1 expression caused by transient ischemic brain injury in rats.

Authors:  C Yao; A J Williams; X-C M Lu; R A Price; B S Cunningham; R Berti; F C Tortella; J R Dave
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10.  Down regulation of sodium channel Na(v)1.1 expression by veratridine and its reversal by a novel sodium channel blocker, RS100642, in primary neuronal cultures.

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Journal:  Neurotox Res       Date:  2003       Impact factor: 3.911

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