Literature DB >> 30071271

Novel E815K knock-in mouse model of alternating hemiplegia of childhood.

Ashley R Helseth1, Arsen S Hunanyan1, Syed Adil2, Molly Linabarger2, Monisha Sachdev3, Elie Abdelnour3, Eric Arehart1, Marlee Szabo3, Jordan Richardson3, William C Wetsel4, Ute Hochgeschwender5, Mohamad A Mikati6.   

Abstract

De novo mutations causing dysfunction of the ATP1A3 gene, which encodes the α3 subunit of Na+/K+-ATPase pump expressed in neurons, result in alternating hemiplegia of childhood (AHC). AHC manifests as paroxysmal episodes of hemiplegia, dystonia, behavioral abnormalities, and seizures. The first aim of this study was to characterize a novel knock-in mouse model (Atp1a3E815K+/-, Matoub, Matb+/-) containing the E815K mutation of the Atp1a3 gene recognized as causing the most severe and second most common phenotype of AHC with increased morbidity and mortality as compared to other mutations. The second aim was to investigate the effects of flunarizine, currently the most effective drug used in AHC, to further validate our model and to help address a question with significant clinical implications that has not been addressed in prior studies. Specifically, many E815K patients have clinical decompensation and catastrophic regression after discontinuing flunarizine therapy; however, it is not known whether this is congruent with the natural course of the disease and is a result of withdrawal from an acute beneficial effect, withdrawal from a long-term protective effect or from a detrimental effect of prior flunarizine exposure. Our behavioral and neurophysiological testing demonstrated that Matb+/- mice express a phenotype that bears a strong resemblance to the E815K phenotype in AHC. In addition, these mice developed spontaneous seizures with high incidence of mortality and required fewer electrical stimulations to reach the kindled state as compared to wild-type littermates. Matb+/- mice treated acutely with flunarizine had reduction in hemiplegic attacks as compared with vehicle-treated mice. After withdrawal of flunarizine, Matb+/- mice that had received flunarizine did neither better nor worse, on behavioral tests, than those who had received vehicle. We conclude that: 1) Our mouse model containing the E815K mutation manifests clinical and neurophysiological features of the most severe form of AHC, 2) Flunarizine demonstrated acute anti-hemiplegic effects but not long-term beneficial or detrimental behavioral effects after it was stopped, and 3) The Matb+/- mouse model can be used to investigate the underlying pathophysiology of ATP1A3 dysfunction and the efficacy of potential treatments for AHC.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ATP1A3; Alternating hemiplegia of childhood; Dystonia; E815K; Epilepsy; Flunarizine; Hippocampus; Kindling; Na/K-ATPase

Mesh:

Substances:

Year:  2018        PMID: 30071271     DOI: 10.1016/j.nbd.2018.07.028

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  10 in total

1.  Polysomnography Findings and Sleep Disorders in Children With Alternating Hemiplegia of Childhood.

Authors:  Sujay Kansagra; Ryan Ghusayni; Bassil Kherallah; Talha Gunduz; Melissa McLean; Lyndsey Prange; Richard M Kravitz; Mohamad A Mikati
Journal:  J Clin Sleep Med       Date:  2019-01-15       Impact factor: 4.062

2.  D-DEMØ, a distinct phenotype caused by ATP1A3 mutations.

Authors:  Lyndsey Prange; Milton Pratt; Kristin Herman; Raphael Schiffmann; David M Mueller; Melissa McLean; Mary Moya Mendez; Nicole Walley; Erin L Heinzen; David Goldstein; Vandana Shashi; Arsen Hunanyan; Vijay Pagadala; Mohamad A Mikati
Journal:  Neurol Genet       Date:  2020-08-04

3.  Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.

Authors:  Mary E Moya-Mendez; David M Mueller; Milton Pratt; Melanie Bonner; Courtney Elliott; Arsen Hunanyan; Gary Kucera; Cheryl Bock; Lyndsey Prange; Joan Jasien; Karen Keough; Vandana Shashi; Marie McDonald; Mohamad A Mikati
Journal:  Epilepsy Behav       Date:  2021-01-23       Impact factor: 2.937

4.  Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3Mashl/+, Mouse Model of Alternating Hemiplegia of Childhood.

Authors:  Arsen S Hunanyan; Boris Kantor; Ram S Puranam; Courtney Elliott; Angela McCall; Justin Dhindsa; Promila Pagadala; Keri Wallace; Jordan Poe; Talha Gunduz; Aravind Asokan; Dwight D Koeberl; Mai K ElMallah; Mohamad A Mikati
Journal:  Hum Gene Ther       Date:  2021-02-12       Impact factor: 5.695

5.  Alternating Hemiplegia of Childhood: A Series of Genetically Confirmed Four Cases from Southern India with Review of Published Literature.

Authors:  Naveen Kumar Bhardwaj; Vykuntaraju K Gowda; Ashwin Vivek Sardesai
Journal:  J Pediatr Genet       Date:  2020-08-13

6.  Alternating Hemiplegia of Childhood: gastrointestinal manifestations and correlation with neurological impairments.

Authors:  Milton Pratt; Julie Uchitel; Nancy McGreal; Kelly Gordon; Lyndsey Prange; Melissa McLean; Richard J Noel; Blaire Rikard; Mary K Rogers Boruta; Mohamad A Mikati
Journal:  Orphanet J Rare Dis       Date:  2020-09-03       Impact factor: 4.123

7.  Decreased content of ascorbic acid (vitamin C) in the brain of knockout mouse models of Na+,K+-ATPase-related neurologic disorders.

Authors:  Keiko Ikeda; Adriana A Tienda; Fiona E Harrison; Kiyoshi Kawakami
Journal:  PLoS One       Date:  2021-02-05       Impact factor: 3.240

8.  ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.

Authors:  Mary E Moya-Mendez; Chiagoziem Ogbonna; Jordan E Ezekian; Michael B Rosamilia; Lyndsey Prange; Caridad de la Uz; Jeffrey J Kim; Taylor Howard; John Garcia; Robert Nussbaum; Rebecca Truty; Thomas E Callis; Emily Funk; Matthew Heyes; Guy de Lisle Dear; Michael P Carboni; Salim F Idriss; Mohamad A Mikati; Andrew P Landstrom
Journal:  J Am Heart Assoc       Date:  2021-08-28       Impact factor: 5.501

9.  Genetically altered animal models for ATP1A3-related disorders.

Authors:  Hannah W Y Ng; Jennifer A Ogbeta; Steven J Clapcote
Journal:  Dis Model Mech       Date:  2021-10-06       Impact factor: 5.732

10.  Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.

Authors:  Simona Balestrini; Mohamad A Mikati; Reyes Álvarez-García-Rovés; Michael Carboni; Arsen S Hunanyan; Bassil Kherallah; Melissa McLean; Lyndsey Prange; Elisa De Grandis; Alessandra Gagliardi; Livia Pisciotta; Michela Stagnaro; Edvige Veneselli; Jaume Campistol; Carmen Fons; Leticia Pias-Peleteiro; Allison Brashear; Charlotte Miller; Raquel Samões; Vesna Brankovic; Quasar S Padiath; Ana Potic; Jacek Pilch; Aikaterini Vezyroglou; Ann M E Bye; Andrew M Davis; Monique M Ryan; Christopher Semsarian; Georgina Hollingsworth; Ingrid E Scheffer; Tiziana Granata; Nardo Nardocci; Francesca Ragona; Alexis Arzimanoglou; Eleni Panagiotakaki; Inês Carrilho; Claudio Zucca; Jan Novy; Karolina Dzieżyc; Marek Parowicz; Maria Mazurkiewicz-Bełdzińska; Sarah Weckhuysen; Roser Pons; Sergiu Groppa; Daniel S Sinden; Geoffrey S Pitt; Andrew Tinker; Michael Ashworth; Zuzanna Michalak; Maria Thom; J Helen Cross; Rosaria Vavassori; Juan P Kaski; Sanjay M Sisodiya
Journal:  Neurology       Date:  2020-09-10       Impact factor: 11.800

  10 in total

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