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NKCC1Chloride Importer Antagonists Attenuate Many Neurological and Psychiatric Disorders

Journal

TRENDS IN NEUROSCIENCES
Volume 40, Issue 9, Pages 536-554

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tins.2017.07.001

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Funding

  1. Bettencourt Schuller Foundation (Paris, France)
  2. AMU-AMIdex (Marseille France)
  3. Simons Foundation for Autism (USA)

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In physiological conditions, adult neurons have low intracellular Cl- [(Cl-) I] levels underlying the gamma-aminobutyric acid (GABA) ergic inhibitory drive. In contrast, neurons have high (Cl (-)) I levels and excitatory GABA actions in a wide range of pathological conditions including spinal cord lesions, chronic pain, brain trauma, cerebrovascular infarcts, autism, Rett and Down syndrome, various types of epilepsies, and other genetic or environmental insults. The diuretic highly specific NKCC1 chloride importer antagonist bumetanide (PubChem CID: 2461) efficiently restores low (Cl-) I levels and attenuates many disorders in experimental conditions and in some clinical trials. Here, I review the mechanisms of action, therapeutic effects, promises, and pitfalls of bumetanide.

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