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SCN10A Mutation in a Patient with Erythromelalgia Enhances C-Fiber Activity Dependent Slowing

Kist, Andreas M. (author)
Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany.;Max Planck Inst Neurobiol, Martinsried, Germany.
Sagafos, Dagrun (author)
Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway.
Rush, Anthony M. (author)
AstraZeneca R&D, Sodertalje, Sweden.;Metrion Biosci, Bldg B501,Babraham Res Campus, Cambridge CB22 3AT, England.
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Neacsu, Cristian (author)
Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany.
Eberhardt, Esther (author)
Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany.;Univ Erlangen Nurnberg, Dept Anesthesiol, Erlangen, Germany.
Schmidt, Roland (author)
Uppsala universitet,Klinisk neurofysiologi
Lunden, Lars Kristian (author)
Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway.
Orstavik, Kristin (author)
Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway.
Kaluza, Luisa (author)
RWTH Aachen Univ Hosp, Inst Physiol, Aachen, Germany.
Meents, Jannis (author)
RWTH Aachen Univ Hosp, Inst Physiol, Aachen, Germany.
Zhang, Zhiping (author)
AstraZeneca R&D, Sodertalje, Sweden.
Carr, Thomas Hedley (author)
AstraZeneca R&D, Cambridge, England.
Salter, Hugh (author)
Karolinska Institutet
Malinowsky, David (author)
AstraZeneca R&D, Sodertalje, Sweden.;Sybicon, Huddinge, Sweden.
Wollberg, Patrik (author)
AstraZeneca R&D, Sodertalje, Sweden.;GE Healthcare, Life Sci, Bjorkgatan 30, SE-75323 Uppsala, Sweden.
Krupp, Johannes (author)
AstraZeneca R&D, Sodertalje, Sweden.;Ipsen Innovat, 5 Ave Canada, F-91940 Les Ulis, France.
Kleggetveit, Inge Petter (author)
Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway.
Schmelz, Martin (author)
Jorum, Ellen (author)
Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway.
Lampert, Angelika (author)
Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany.;RWTH Aachen Univ Hosp, Inst Physiol, Aachen, Germany.
Namer, Barbara (author)
Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany.;Heidelberg Univ, Dept Anesthesiol Mannheim, Mannheim, Germany.
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Univ Erlangen Nurnberg, Inst Physiol & Pathophysiol, Erlangen, Germany;Max Planck Inst Neurobiol, Martinsried, Germany. Oslo Univ Hosp, Rikshosp, Dept Neurol, Clin Neurophysiol Sect, Oslo, Norway. (creator_code:org_t)
2016-09-06
2016
English.
In: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 11:9
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Gain-of-function mutations in the tetrodotoxin (TTX) sensitive voltage-gated sodium channel (Nav) Nav1.7 have been identified as a key mechanism underlying chronic pain in inherited erythromelalgia. Mutations in TTX resistant channels, such as Nav1.8 or Nav1.9, were recently connected with inherited chronic pain syndromes. Here, we investigated the effects of the p.M650K mutation in Nav1.8 in a 53 year old patient with erythromelalgia by micro-neurography and patch-clamp techniques. Recordings of the patient's peripheral nerve fibers showed increased activity dependent slowing (ADS) in CMi and less spontaneous firing compared to a control group of erythromelalgia patients without Nav mutations. To evaluate the impact of the p. M650K mutation on neuronal firing and channel gating, we performed current and voltage-clamp recordings on transfected sensory neurons (DRGs) and neuroblastoma cells. The p. M650K mutation shifted steady-state fast inactivation of Nav1.8 to more hyperpolarized potentials and did not significantly alter any other tested gating behaviors. The AP half-width was significantly broader and the stimulated action potential firing rate was reduced for M650K transfected DRGs compared to WT. We discuss the potential link between enhanced steady state fast inactivation, broader action potential width and the potential physiological consequences.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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