Literature DB >> 22805230

The use of aminopyridines in neurological disorders.

Saam Sedehizadeh1, Michael Keogh, Paul Maddison.   

Abstract

Aminopyridines are members of a family of monoamino and diamino derivatives of pyridine, and their principal mechanism of action is dose-dependent blockade of voltage-gated potassium channels, in particular, fast voltage-gated potassium channels. To date, only 2 main broad-spectrum potassium channel blockers, 4-aminopyridine (4-AP) and 3,4-diaminopyridine (3,4-DAP), have been used as investigational new drugs in various neurological diseases. More recently, licensed versions of these compounds including dalfampridine extended release (Fampyra, Biogen Idec) for the improvement of walking in adult patients with multiple sclerosis, and amifampridine (Firdapse, Biomarin Europe Ltd) for the treatment of Lambert-Eaton myasthenic syndrome have been released, and the costs associated with using these new products highlights the importance of evaluating the clinically meaningful treatment effects of these drugs.The current review summarizes the evidence of aminopyridine use in neurological conditions and in particular presents a systematic review of all randomized trials of 3,4-DAP in Lambert-Eaton myasthenic syndrome to determine the efficacy of this treatment using meta-analysis of clinical and electrophysiological end points.

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Year:  2012        PMID: 22805230     DOI: 10.1097/WNF.0b013e31825a68c5

Source DB:  PubMed          Journal:  Clin Neuropharmacol        ISSN: 0362-5664            Impact factor:   1.592


  9 in total

1.  Targeting ion channels for the treatment of autoimmune neuroinflammation.

Authors:  Stefan Bittner; Sven G Meuth
Journal:  Ther Adv Neurol Disord       Date:  2013-09       Impact factor: 6.570

Review 2.  Lambert-Eaton myasthenic syndrome: mouse passive-transfer model illuminates disease pathology and facilitates testing therapeutic leads.

Authors:  Stephen D Meriney; Tyler B Tarr; Kristine S Ojala; Man Wu; Yizhi Li; David Lacomis; Adolfo Garcia-Ocaña; Mary Liang; Guillermo Valdomir; Peter Wipf
Journal:  Ann N Y Acad Sci       Date:  2017-11-10       Impact factor: 5.691

3.  4-aminopyridine improves lower urinary tract symptoms in a patient with benign prostatic hyperplasia and downbeat nystagmus syndrome.

Authors:  Michael Strupp; Katharina Feil; Stanislavs Bardins; Raphaela Waidelich
Journal:  Int Neurourol J       Date:  2014-12-29       Impact factor: 2.835

4.  Complete reversal of Lambert-Eaton myasthenic syndrome synaptic impairment by the combined use of a K+ channel blocker and a Ca2+ channel agonist.

Authors:  Tyler B Tarr; David Lacomis; Stephen W Reddel; Mary Liang; Guillermo Valdomir; Michael Frasso; Peter Wipf; Stephen D Meriney
Journal:  J Physiol       Date:  2014-07-11       Impact factor: 5.182

5.  New Cav2 calcium channel gating modifiers with agonist activity and therapeutic potential to treat neuromuscular disease.

Authors:  Man Wu; Hayley V White; Blake A Boehm; Christopher J Meriney; Kaylan Kerrigan; Michael Frasso; Mary Liang; Erika M Gotway; Madeleine R Wilcox; Jon W Johnson; Peter Wipf; Stephen D Meriney
Journal:  Neuropharmacology       Date:  2017-12-12       Impact factor: 5.250

Review 6.  Synaptic Pathophysiology and Treatment of Lambert-Eaton Myasthenic Syndrome.

Authors:  Tyler B Tarr; Peter Wipf; Stephen D Meriney
Journal:  Mol Neurobiol       Date:  2014-09-09       Impact factor: 5.590

7.  Inverse Modulation of Neuronal Kv12.1 and Kv11.1 Channels by 4-Aminopyridine and NS1643.

Authors:  Marlen Dierich; Saskia Evers; Bettina U Wilke; Michael G Leitner
Journal:  Front Mol Neurosci       Date:  2018-01-30       Impact factor: 5.639

8.  4-aminopyridine does not enhance flocculus function in tottering, a mouse model of vestibulocerebellar dysfunction and ataxia.

Authors:  John S Stahl; Zachary C Thumser
Journal:  PLoS One       Date:  2013-02-25       Impact factor: 3.240

9.  Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels.

Authors:  Xueyong Wang; Steven R A Burke; Robert J Talmadge; Andrew A Voss; Mark M Rich
Journal:  J Gen Physiol       Date:  2020-05-04       Impact factor: 4.086

  9 in total

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