Literature DB >> 29197650

KCC2, epileptiform synchronization, and epileptic disorders.

Graziella Di Cristo1, Patricia N Awad2, Shabnam Hamidi3, Massimo Avoli4.   

Abstract

The K+-Cl- co-transporter KCC2 is a neuron-specific, Cl- extruder that uses K+ gradient for maintaining low intracellular [Cl-]. It is indeed well established that sustaining an outwardly-directed electrochemical Cl- gradient across the neuronal membrane is fundamental for a proper function of postsynaptic GABAA receptor signaling. In particular, studies in the last two decades have shown that KCC2 activity is important to maintain a hyperpolarizing GABAergic neurotransmission. Conversely, low KCC2 activity should lead to depolarizing, and under specific conditions, excitatory GABAergic transmission. Not surprisingly given the critical role of KCC2 in regulating the inhibitory drive, alterations in its expression levels and activity are linked with epilepsy. Here, we will first summarize data regarding the role of KCC2 in epileptiform synchronization. Next, we will review evidence indicating that KCC2 expression and function are altered in chronic epileptic disorders, both in the developing and adult brain. We will also go through recent findings regarding the molecular mechanisms underlying the changes in KCC2 activity that occur following seizures. Finally, we will consider the modulation of KCC2 function as a potential, novel therapeutic target for the treatment of epileptic disorders. Crown
Copyright © 2017. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Context-specific; Epilepsy; GABA; Juvenile; KCC2; Pathology-specific; Seizures

Mesh:

Substances:

Year:  2017        PMID: 29197650     DOI: 10.1016/j.pneurobio.2017.11.002

Source DB:  PubMed          Journal:  Prog Neurobiol        ISSN: 0301-0082            Impact factor:   11.685


  22 in total

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Review 2.  G protein-coupled receptors in acquired epilepsy: Druggability and translatability.

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3.  Low-voltage fast seizures in humans begin with increased interneuron firing.

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4.  ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual Disability.

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Review 5.  Preclinical insights into therapeutic targeting of KCC2 for disorders of neuronal hyperexcitability.

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Journal:  Transl Psychiatry       Date:  2018-11-29       Impact factor: 6.222

7.  Loss of MicroRNA-137 Impairs the Homeostasis of Potassium in Neurons via KCC2.

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8.  ER stress-induced modulation of neural activity and seizure susceptibility is impaired in a fragile X syndrome mouse model.

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Journal:  Neurobiol Dis       Date:  2021-07-23       Impact factor: 7.046

9.  Ketogenic Diet Provided During Three Months Increases KCC2 Expression but Not NKCC1 in the Rat Dentate Gyrus.

Authors:  Leticia Granados-Rojas; Karina Jerónimo-Cruz; Tarsila Elizabeth Juárez-Zepeda; Miguel Tapia-Rodríguez; Armando R Tovar; Rodolfo Rodríguez-Jurado; Liliana Carmona-Aparicio; Noemí Cárdenas-Rodríguez; Elvia Coballase-Urrutia; Matilde Ruíz-García; Pilar Durán
Journal:  Front Neurosci       Date:  2020-07-07       Impact factor: 4.677

10.  KCC2 Regulates Dendritic Spine Formation in a Brain-Region Specific and BDNF Dependent Manner.

Authors:  Patricia Nora Awad; Clara Akofa Amegandjin; Joanna Szczurkowska; Josianne Nuñes Carriço; Antônia Samia Fernandes do Nascimento; Elie Baho; Bidisha Chattopadhyaya; Laura Cancedda; Lionel Carmant; Graziella Di Cristo
Journal:  Cereb Cortex       Date:  2018-11-01       Impact factor: 5.357

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