Literature DB >> 26050032

The GABAA Receptor as a Therapeutic Target for Neurodevelopmental Disorders.

Sien Braat1, R Frank Kooy2.   

Abstract

Intellectual disability, autism spectrum disorder, and epilepsy are prime examples of neurodevelopmental disorders that collectively affect a significant percentage of the world population. Recent technological breakthroughs allowed the elucidation of the genetic causes of many of these disorders. As neurodevelopmental disorders are genetically heterogeneous, the development of rational therapy is extremely challenging. Fortunately, many causative genes are interconnected and cluster in specific cellular pathways. Targeting a common node in such a network would allow us to interfere with a series of related neurodevelopmental disorders at once. Here, we argue that the GABAergic system is disturbed in many neurodevelopmental disorders, including fragile X syndrome, Rett syndrome, and Dravet syndrome, and is a key candidate target for therapeutic intervention. Many drugs that modulate the GABAergic system have already been tested in animal models with encouraging outcomes and are readily available for clinical trials.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26050032     DOI: 10.1016/j.neuron.2015.03.042

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  105 in total

Review 1.  Genetic studies in intellectual disability and related disorders.

Authors:  Lisenka E L M Vissers; Christian Gilissen; Joris A Veltman
Journal:  Nat Rev Genet       Date:  2015-10-27       Impact factor: 53.242

2.  Inhibitory interneurons mediate autism-associated behaviors via 4E-BP2.

Authors:  Shane Wiebe; Anmol Nagpal; Vinh T Truong; Jeehyun Park; Agnieszka Skalecka; Alexander J He; Karine Gamache; Arkady Khoutorsky; Ilse Gantois; Nahum Sonenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2019-08-19       Impact factor: 11.205

3.  Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome.

Authors:  Jonathan W Lovelace; Maham Rais; Arnold R Palacios; Xinghao S Shuai; Steven Bishay; Otilia Popa; Patricia S Pirbhoy; Devin K Binder; David L Nelson; Iryna M Ethell; Khaleel A Razak
Journal:  Cereb Cortex       Date:  2020-03-14       Impact factor: 5.357

4.  Developmental timing and critical windows for the treatment of psychiatric disorders.

Authors:  Oscar Marín
Journal:  Nat Med       Date:  2016-10-26       Impact factor: 53.440

5.  Rapid Throughput Analysis of GABAA Receptor Subtype Modulators and Blockers Using DiSBAC1(3) Membrane Potential Red Dye.

Authors:  Atefeh Mousavi Nik; Brandon Pressly; Vikrant Singh; Shane Antrobus; Susan Hulsizer; Michael A Rogawski; Heike Wulff; Isaac N Pessah
Journal:  Mol Pharmacol       Date:  2017-04-20       Impact factor: 4.436

Review 6.  Emerging connections between cerebellar development, behaviour and complex brain disorders.

Authors:  Aaron Sathyanesan; Joy Zhou; Joseph Scafidi; Detlef H Heck; Roy V Sillitoe; Vittorio Gallo
Journal:  Nat Rev Neurosci       Date:  2019-05       Impact factor: 34.870

7.  Arbaclofen in Children and Adolescents with Autism Spectrum Disorder: A Randomized, Controlled, Phase 2 Trial.

Authors:  Jeremy Veenstra-VanderWeele; Edwin H Cook; Bryan H King; Peter Zarevics; Maryann Cherubini; Karen Walton-Bowen; Mark F Bear; Paul P Wang; Randall L Carpenter
Journal:  Neuropsychopharmacology       Date:  2016-10-17       Impact factor: 7.853

8.  Deficits in the activity of presynaptic γ-aminobutyric acid type B receptors contribute to altered neuronal excitability in fragile X syndrome.

Authors:  Ji-Yong Kang; Jayashree Chadchankar; Thuy N Vien; Michelle I Mighdoll; Thomas M Hyde; Robert J Mather; Tarek Z Deeb; Menelas N Pangalos; Nicholas J Brandon; John Dunlop; Stephen J Moss
Journal:  J Biol Chem       Date:  2017-02-17       Impact factor: 5.157

9.  Decreased surface expression of the δ subunit of the GABAA receptor contributes to reduced tonic inhibition in dentate granule cells in a mouse model of fragile X syndrome.

Authors:  Nianhui Zhang; Zechun Peng; Xiaoping Tong; A Kerstin Lindemeyer; Yliana Cetina; Christine S Huang; Richard W Olsen; Thomas S Otis; Carolyn R Houser
Journal:  Exp Neurol       Date:  2017-08-16       Impact factor: 5.330

10.  Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.

Authors:  Wei-Hsiang Huang; Casey J Guenthner; Jin Xu; Tiffany Nguyen; Lindsay A Schwarz; Alex W Wilkinson; Or Gozani; Howard Y Chang; Mehrdad Shamloo; Liqun Luo
Journal:  Neuron       Date:  2016-09-29       Impact factor: 17.173

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