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Activation of axonal Kv7 channels in human peripheral nerve by flupirtine but not placebo - therapeutic potential for peripheral neuropathies: results of a randomised controlled trial.
- Source :
-
Journal of translational medicine [J Transl Med] 2013 Feb 08; Vol. 11, pp. 34. Date of Electronic Publication: 2013 Feb 08. - Publication Year :
- 2013
-
Abstract
- Background: Flupirtine is an analgesic with muscle-relaxing properties that activates Kv7 potassium channels. Kv7 channels are expressed along myelinated and unmyelinated peripheral axons where their activation is expected to reduce axonal excitability and potentially contribute to flupirtine's clinical profile.<br />Trial Design: To investigate the electrical excitability of peripheral myelinated axons following orally administered flupirtine, in-vitro experiments on isolated peripheral nerve segments were combined with a randomised, double-blind, placebo-controlled, phase I clinical trial (RCT).<br />Methods: Threshold tracking was used to assess the electrical excitability of myelinated axons in isolated segments of human sural nerve in vitro and motoneurones to abductor pollicis brevis (APB) in situ in healthy subjects. In addition, the effect of flupirtine on ectopic action potential generation in myelinated axons was examined using ischemia of the lower arm.<br />Results: Flupirtine (3-30 μM) shortened the relative refractory period and increased post-conditioned superexcitability in human myelinated axons in vitro. Similarly, in healthy subjects the relative refractory period of motoneurones to APB was reduced 2 hours after oral flupirtine but not following placebo. Whether this effect was due to a direct action of flupirtine on peripheral axons or temperature could not be resolved. Flupirtine (200 mg p.o.) also reduced ectopic axonal activity induced by 10 minutes of lower arm ischemia. In particular, high frequency (ca. 200 Hz) components of EMG were reduced in the post-ischemic period. Finally, visual analogue scale ratings of sensations perceived during the post-ischemic period were reduced following flupirtine (200 mg p.o.).<br />Conclusions: Clinical doses of flupirtine reduce the excitability of peripheral myelinated axons.<br />Trial Registration: ClinicalTrials registration is NCT01450865.
- Subjects :
- Administration, Oral
Aged
Aged, 80 and over
Axons drug effects
Axons pathology
Double-Blind Method
Electromyography
Female
Humans
Ischemia
Male
Middle Aged
Muscle Relaxants, Central therapeutic use
Myelin Sheath drug effects
Myelin Sheath metabolism
Peripheral Nervous System Diseases drug therapy
Sural Nerve physiology
Aminopyridines therapeutic use
Axons metabolism
KCNQ1 Potassium Channel metabolism
Peripheral Nerves drug effects
Peripheral Nervous System Diseases metabolism
Sural Nerve drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1479-5876
- Volume :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of translational medicine
- Publication Type :
- Academic Journal
- Accession number :
- 23394517
- Full Text :
- https://doi.org/10.1186/1479-5876-11-34