Home LiteratureArticle Details
PMID: 15843617 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering.

Weisz CJ, Raike RS, Soria-Jasso LE, Hess EJ

Abstract

Humans with the disorder episodic ataxia type 2 (EA2) and the tottering mouse mutant exhibit episodic attacks induced by emotional and chemical stress. Both the human and mouse disorders result from mutations in CACNA1A, the gene encoding the alpha(1)2.1 subunit of Ca(v)2.1 voltage-gated calcium channels. These mutations predict reduced calcium currents, particularly in cerebellar Purkinje cells, where these channels are most abundant. 4-Aminopyridine (4-AP), a nonselective blocker of K(v) voltage-gated potassium channels, alleviates attacks of ataxia in EA2 patients. To test the specificity of the effect for K(v) channels, aminopyridine analogs were assessed for their ability to ameliorate attacks of dyskinesia in tottering mice. 4-AP and 3,4-diaminopyridine (3,4-DiAP), which have relatively high affinities for K(v) channels, reduced the frequency of restraint- and caffeine-induced attacks. Furthermore, microinjection of 3,4-DiAP into the cerebellum completely blocked attacks in tottering mice. Other aminopyridine analogs reduced attack frequency but, consistent with their lower affinities for K(v) channels, required comparatively higher doses. These results suggest that aminopyridines block tottering mouse attacks via cerebellar K(v) channels. That both stress- and caffeine-induced attacks were blocked by aminopyridines suggests that these triggers act via similar mechanisms. Although 4-AP and 3,4-DiAP were effective in preventing attacks in tottering mice, these compounds did not affect the severity of "breakthrough" attacks that occurred in the presence of a drug. These results suggest that the aminopyridines increase the threshold for attack initiation without mitigating the character of the attack, indicating that attack initiation is mediated by mechanisms that are independent of the neurological phenotype.

MeSH Terms
4-Aminopyridine/administration & dosage,chemistry Analysis of Variance Animals Behavior, Animal Caffeine/adverse effects Calcium Channels, N-Type Calcium Channels, P-Type/genetics Calcium Channels, Q-Type/genetics Cerebellum/drug effects Disease Models, Animal Dose-Response Relationship, Drug Drug Interactions Dyskinesias/etiology,genetics,prevention & control Mice Mice, Inbred C57BL Mice, Neurologic Mutants Microinjections/methods Mutation Potassium Channel Blockers/administration & dosage
Chemicals
Calcium Channels, N-Type Calcium Channels, P-Type Calcium Channels, Q-Type Potassium Channel Blockers voltage-dependent calcium channel (P-Q type) Caffeine 4-Aminopyridine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Weisz Catherine J C
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.
Raike Robert S
Soria-Jasso Luis E
Hess Ellen J
References (34)
34 references, click to expand
  1. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
    Neurology. 1999 Jun 10;52(9):1816-21 PMID: 10371528
  2. Calcium channelopathies in the central nervous system.
    Curr Opin Neurobiol. 1999 Jun;9(3):274-80 PMID: 10395579
  3. A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.
    Neurology. 1999 Jul 13;53(1):38-43 PMID: 10408534
  4. Molecular diversity of K+ channels.
    Ann N Y Acad Sci. 1999 Apr 30;868:233-85 PMID: 10414301
  5. Episodic movement disorders as channelopathies.
    Mov Disord. 2000 May;15(3):429-33 PMID: 10830404
  6. Calcium channel agonists and dystonia in the mouse.
    Mov Disord. 2000 May;15(3):542-51 PMID: 10830422
  7. Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
    Am J Hum Genet. 2001 Mar;68(3):759-64 PMID: 11179022
  8. Highly 4-aminopyridine sensitive delayed rectifier current modulates the excitability of guinea pig cerebellar Purkinje cells.
    Exp Brain Res. 2001 Aug;139(4):419-25 PMID: 11534865
  9. Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
    Lancet. 2001 Sep 8;358(9284):801-7 PMID: 11564488
  10. Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
    Neurology. 2001 Nov 27;57(10):1843-8 PMID: 11723274
  11. Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia.
    J Biol Chem. 2002 Mar 1;277(9):6960-6 PMID: 11742003
  12. Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.
    Pharmacol Biochem Behav. 2002 Oct;73(3):631-7 PMID: 12151038
  13. Treatment of downbeat nystagmus with 3,4-diaminopyridine: a placebo-controlled study.
    Neurology. 2003 Jul 22;61(2):165-70 PMID: 12874393
  14. Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.
    Neuron. 1992 May;8(5):891-7 PMID: 1316765
  15. Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
    Ann Neurol. 2003 Dec;54(6):725-31 PMID: 14681882
  16. Dendritic control of spontaneous bursting in cerebellar Purkinje cells.
    J Neurosci. 2004 Apr 7;24(14):3511-21 PMID: 15071098
  17. Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.
    Neurology. 2004 May 11;62(9):1623-5 PMID: 15136697
  18. Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.
    Ann Neurol. 2004 Aug;56(2):213-20 PMID: 15293273
  19. Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy.
    Neuron. 2004 Aug 5;43(3):387-400 PMID: 15294146
  20. Identification of a mutation in the gene causing hyperkalemic periodic paralysis.
    Cell. 1991 Nov 29;67(5):1021-7 PMID: 1659948
  21. On the active form of 4-aminopyridine: block of K+ currents in rabbit Schwann cells.
    J Physiol. 1991 Feb;433:183-205 PMID: 1841938
  22. Effects of several aminopyridines and analogs on the calcium dependence of synaptic transmission.
    J Pharmacol Exp Ther. 1984 Mar;228(3):573-8 PMID: 6323673
  23. Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels.
    Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10576-80 PMID: 7524096
  24. Episodic ataxias as channelopathies.
    Ann Neurol. 1995 Mar;37(3):285-7 PMID: 7535034
  25. Localization of mRNAs of voltage-dependent Ca(2+)-channels: four subtypes of alpha 1- and beta-subunits in developing and mature rat brain.
    Brain Res Mol Brain Res. 1995 May;30(1):1-16 PMID: 7609630
  26. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.
    Cell. 1994 Jun 17;77(6):863-8 PMID: 8004673
  27. The expression of neuronal voltage-dependent calcium channels in human cerebellum.
    Brain Res Mol Brain Res. 1995 Dec 28;34(2):271-82 PMID: 8750830
  28. A method for determining 4-aminopyridine in plasma: pharmacokinetics in anaesthetized guinea pigs after intravenous administration.
    Biomed Chromatogr. 1996 May-Jun;10(3):111-6 PMID: 8792860
  29. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
    Cell. 1996 Nov 1;87(3):543-52 PMID: 8898206
  30. Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
    Cell. 1996 Nov 15;87(4):607-17 PMID: 8929530
  31. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system.
    Neuromuscul Disord. 1997 Jun;7(4):250-5 PMID: 9196907
  32. Episodic ataxia and channelopathies.
    Brain Dev. 1998 Jan;20(1):9-13 PMID: 9533553
  33. Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse.
    Neuroscience. 1998 Aug;85(3):773-83 PMID: 9639271
  34. Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.
    J Biol Chem. 1998 Dec 25;273(52):34857-67 PMID: 9857013
Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
1529-2401
Published
2005-04-20
Pages
4141-5
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6724952
Subset
IM
Grants
NINDS NIH HHS · R01 NS033592 · United States
NINDS NIH HHS · NS33592 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]