Literature DB >> 25221437

Translating cerebellar Purkinje neuron physiology to progress in dominantly inherited ataxia.

Ravi Chopra1, Vikram G Shakkottai1.   

Abstract

The cerebellum is an important structure for accurate control and timing of movement, and Purkinje neurons in the cerebellar cortex are key players in cerebellar motor control. Cerebellar dysfunction can result in ataxia, a disorder characterized by postural instability, gait disturbances and motor incoordination. Cerebellar ataxia is a symptom of a number of conditions, and the emerging evidence that Purkinje neuron dysfunction, in particular, abnormal Purkinje neuron repetitive firing, is a major driver of motor dysfunction in a subset of dominantly inherited ataxias is dicussed. Abnormalities in Purkinje neuron excitability that are observed in mouse models of each of these disorders, and where appropriate describe studies linking particular ion channels to aberrant excitability are also discussed. Common mechanisms of dysfunction and speculate about potential therapeutic targets, suggesting that Purkinje neuron firing abnormalities are a novel target for improving motor dysfunction in patients with some forms of dominantly inherited ataxia are proposed.

Entities:  

Keywords:  Purkinje neuron; atrophy; cerebellum; dominantly inherited ataxia; intrinsic excitability; ion channel; pacemaking; polyglutamine disorder; spinocerebellar ataxia

Year:  2014        PMID: 25221437      PMCID: PMC4159172          DOI: 10.2217/fnl.14.6

Source DB:  PubMed          Journal:  Future Neurol        ISSN: 1479-6708


  46 in total

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Authors:  Timothy O'Leary; Alex H Williams; Jonathan S Caplan; Eve Marder
Journal:  Proc Natl Acad Sci U S A       Date:  2013-06-24       Impact factor: 11.205

Review 2.  Machado-Joseph disease/spinocerebellar ataxia type 3.

Authors:  Henry Paulson
Journal:  Handb Clin Neurol       Date:  2012

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Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1968-09       Impact factor: 2.714

4.  The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract.

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Journal:  Hum Mol Genet       Date:  2001-01-01       Impact factor: 6.150

Review 5.  Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives.

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Journal:  Mol Neurobiol       Date:  2012-09-21       Impact factor: 5.590

6.  Disruption of the olivo-cerebellar circuit by Purkinje neuron-specific ablation of BK channels.

Authors:  Xiaowei Chen; Yury Kovalchuk; Helmuth Adelsberger; Horst A Henning; Matthias Sausbier; Georg Wietzorrek; Peter Ruth; Yosef Yarom; Arthur Konnerth
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-21       Impact factor: 11.205

Review 7.  The core Dravet syndrome phenotype.

Authors:  Charlotte Dravet
Journal:  Epilepsia       Date:  2011-04       Impact factor: 5.864

8.  In vivo evidence of cerebellar atrophy and cerebral white matter loss in Huntington disease.

Authors:  C Fennema-Notestine; S L Archibald; M W Jacobson; J Corey-Bloom; J S Paulsen; G M Peavy; A C Gamst; J M Hamilton; D P Salmon; T L Jernigan
Journal:  Neurology       Date:  2004-09-28       Impact factor: 9.910

Review 9.  Pathways to motor incoordination: the inherited ataxias.

Authors:  Franco Taroni; Stefano DiDonato
Journal:  Nat Rev Neurosci       Date:  2004-08       Impact factor: 34.870

10.  FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons.

Authors:  Vikram G Shakkottai; Maolei Xiao; Lin Xu; Michael Wong; Jeanne M Nerbonne; David M Ornitz; Kelvin A Yamada
Journal:  Neurobiol Dis       Date:  2008-10-01       Impact factor: 5.996

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  15 in total

1.  Atrophic degeneration of cerebellum impairs both the reactive and the proactive control of movement in the stop signal paradigm.

Authors:  Giusy Olivito; Emiliano Brunamonti; Silvia Clausi; Pierpaolo Pani; Francesca R Chiricozzi; Margherita Giamundo; Marco Molinari; Maria Leggio; Stefano Ferraina
Journal:  Exp Brain Res       Date:  2017-07-17       Impact factor: 1.972

2.  Protein kinase C activity is a protective modifier of Purkinje neuron degeneration in cerebellar ataxia.

Authors:  Ravi Chopra; Aaron H Wasserman; Stefan M Pulst; Chris I De Zeeuw; Vikram G Shakkottai
Journal:  Hum Mol Genet       Date:  2018-04-15       Impact factor: 6.150

3.  ATXN1-CIC Complex Is the Primary Driver of Cerebellar Pathology in Spinocerebellar Ataxia Type 1 through a Gain-of-Function Mechanism.

Authors:  Maxime W C Rousseaux; Tyler Tschumperlin; Hsiang-Chih Lu; Elizabeth P Lackey; Vitaliy V Bondar; Ying-Wooi Wan; Qiumin Tan; Carolyn J Adamski; Jillian Friedrich; Kirk Twaroski; Weili Chen; Jakub Tolar; Christine Henzler; Ajay Sharma; Aleksandar Bajić; Tao Lin; Lisa Duvick; Zhandong Liu; Roy V Sillitoe; Huda Y Zoghbi; Harry T Orr
Journal:  Neuron       Date:  2018-03-08       Impact factor: 17.173

4.  Structural cerebellar correlates of cognitive functions in spinocerebellar ataxia type 2.

Authors:  G Olivito; M Lupo; C Iacobacci; S Clausi; S Romano; M Masciullo; M Molinari; M Cercignani; M Bozzali; M Leggio
Journal:  J Neurol       Date:  2018-01-22       Impact factor: 4.849

Review 5.  Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2.

Authors:  Polina A Egorova; Ilya B Bezprozvanny
Journal:  Neurotherapeutics       Date:  2019-10       Impact factor: 7.620

Review 6.  Polyglutamine spinocerebellar ataxias - from genes to potential treatments.

Authors:  Henry L Paulson; Vikram G Shakkottai; H Brent Clark; Harry T Orr
Journal:  Nat Rev Neurosci       Date:  2017-08-17       Impact factor: 34.870

Review 7.  Precision medicine in spinocerebellar ataxias: treatment based on common mechanisms of disease.

Authors:  David D Bushart; Geoffrey G Murphy; Vikram G Shakkottai
Journal:  Ann Transl Med       Date:  2016-01

8.  A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia.

Authors:  Marie Coutelier; Iulia Blesneac; Arnaud Monteil; Marie-Lorraine Monin; Kunie Ando; Emeline Mundwiller; Alfredo Brusco; Isabelle Le Ber; Mathieu Anheim; Anna Castrioto; Charles Duyckaerts; Alexis Brice; Alexandra Durr; Philippe Lory; Giovanni Stevanin
Journal:  Am J Hum Genet       Date:  2015-10-08       Impact factor: 11.025

9.  Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2.

Authors:  James M Dell'Orco; Stefan M Pulst; Vikram G Shakkottai
Journal:  Hum Mol Genet       Date:  2017-10-15       Impact factor: 6.150

10.  A Chlorzoxazone-Baclofen Combination Improves Cerebellar Impairment in Spinocerebellar Ataxia Type 1.

Authors:  David D Bushart; Haoran Huang; Luke J Man; Logan M Morrison; Vikram G Shakkottai
Journal:  Mov Disord       Date:  2020-11-05       Impact factor: 10.338

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