Literature DB >> 15867950

Retigabine: chemical synthesis to clinical application.

G Blackburn-Munro1, W Dalby-Brown, N R Mirza, J D Mikkelsen, R E Blackburn-Munro.   

Abstract

Retigabine [D23129; N-(2-amino-4-(4-fluorobenzylamino)-phenyl)carbamic acid ethyl ester] is an antiepileptic drug with a recently described novel mechanism of action that involves opening of neuronal K(V)7.2-7.5 (formerly KCNQ2-5) voltage-activated K(+) channels. These channels (primarily K(V)7.2/7.3) enable generation of the M-current, a subthreshold K(+) current that serves to stabilize the membrane potential and control neuronal excitability. In this regard, retigabine has been shown to have a broad-spectrum of activity in animal models of electrically-induced (amygdala-kindling, maximal electroshock) and chemically-induced (pentylenetetrazole, picrotoxin, NMDA) epileptic seizures. These encouraging results suggest that retigabine may also prove useful in the treatment of other diseases associated with neuronal hyperexcitability. Neuropathic pain conditions are characterized by pathological changes in sensory pathways, which favor action potential generation and enhanced pain transmission. Although sometimes difficult to treat with conventional analgesics, antiepileptics can relieve some symptoms of neuropathic pain. A number of recent studies have reported that retigabine can relieve pain-like behaviors (hyperalgesia and allodynia) in animal models of neuropathic pain. Neuronal activation within several key structures within the CNS can also be observed in various animal models of anxiety. Moreover, amygdala-kindled rats, which have a lowered threshold for neuronal activation, also display enhanced anxiety-like responses. Retigabine dose-dependently reduces unconditioned anxiety-like behaviors when assessed in the mouse marble burying test and zero maze. Early clinical studies have indicated that retigabine is rapidly absorbed and distributed, and is resistant to first pass metabolism. Tolerability is good in humans when titrated up to its therapeutic dose range (600-1200 mg/day). No tolerance, dependence or withdrawal potential has been reported, although adverse effects can include mild dizziness, headache, nausea and somnolence. Thus, retigabine may prove to be useful in the treatment of a diverse range of disease states in which neuronal hyperexcitability is a common underlying factor.

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Year:  2005        PMID: 15867950      PMCID: PMC6741764          DOI: 10.1111/j.1527-3458.2005.tb00033.x

Source DB:  PubMed          Journal:  CNS Drug Rev        ISSN: 1080-563X


  38 in total

1.  Expression and function of the K+ channel KCNQ genes in human arteries.

Authors:  Fu Liang Ng; Alison J Davis; Thomas A Jepps; Maksym I Harhun; Shuk Yin Yeung; Andrew Wan; Marcus Reddy; David Melville; Antonio Nardi; Teck K Khong; Iain A Greenwood
Journal:  Br J Pharmacol       Date:  2011-01       Impact factor: 8.739

2.  Electrophysiological Phenotype Characterization of Human iPSC-Derived Neuronal Cell Lines by Means of High-Density Microelectrode Arrays.

Authors:  Silvia Ronchi; Alessio Paolo Buccino; Gustavo Prack; Sreedhar Saseendran Kumar; Manuel Schröter; Michele Fiscella; Andreas Hierlemann
Journal:  Adv Biol (Weinh)       Date:  2021-01-14

Review 3.  Diverse mechanisms of antiepileptic drugs in the development pipeline.

Authors:  Michael A Rogawski
Journal:  Epilepsy Res       Date:  2006-04-18       Impact factor: 3.045

Review 4.  Kv7 channels: interaction with dopaminergic and serotonergic neurotransmission in the CNS.

Authors:  Henrik H Hansen; Olivier Waroux; Vincent Seutin; Thomas J Jentsch; Susana Aznar; Jens D Mikkelsen
Journal:  J Physiol       Date:  2008-01-03       Impact factor: 5.182

Review 5.  Action potential initiation and propagation: upstream influences on neurotransmission.

Authors:  G J Kress; S Mennerick
Journal:  Neuroscience       Date:  2008-03-19       Impact factor: 3.590

6.  A study of subunit selectivity, mechanism and site of action of the delta selective compound 2 (DS2) at human recombinant and rodent native GABA(A) receptors.

Authors:  M L Jensen; K A Wafford; A R Brown; D Belelli; J J Lambert; N R Mirza
Journal:  Br J Pharmacol       Date:  2013-03       Impact factor: 8.739

Review 7.  Voltage-gated potassium channels at the crossroads of neuronal function, ischemic tolerance, and neurodegeneration.

Authors:  Niyathi Hegde Shah; Elias Aizenman
Journal:  Transl Stroke Res       Date:  2013-11-19       Impact factor: 6.829

8.  Chronic Pharmacological Increase of Neuronal Activity Improves Sensory-Motor Dysfunction in Spinal Muscular Atrophy Mice.

Authors:  Christian M Simon; Beatriz Blanco-Redondo; Jannik M Buettner; John G Pagiazitis; Emily V Fletcher; Josiane K Sime Longang; George Z Mentis
Journal:  J Neurosci       Date:  2020-11-20       Impact factor: 6.167

9.  Discovery of Aromatic Carbamates that Confer Neuroprotective Activity by Enhancing Autophagy and Inducing the Anti-Apoptotic Protein B-Cell Lymphoma 2 (Bcl-2).

Authors:  Nihar Kinarivala; Ronak Patel; Rose-Mary Boustany; Abraham Al-Ahmad; Paul C Trippier
Journal:  J Med Chem       Date:  2017-11-22       Impact factor: 7.446

Review 10.  Voltage-gated potassium channels as therapeutic targets.

Authors:  Heike Wulff; Neil A Castle; Luis A Pardo
Journal:  Nat Rev Drug Discov       Date:  2009-12       Impact factor: 84.694

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