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Neonatal seizures are different from adult seizures, and many antiepileptic drugs that are effective in adults often fail to treat neonates. Here, we report that gluconate inhibits neonatal seizure by inhibiting CLC-3 chloride channels. We detect a voltage-dependent outward rectifying Cl current mediated by CLC-3 Cl channels in early developing brains but not adult mouse brains. Blocking CLC-3 Cl channels by gluconate inhibits seizure activity both in neonatal brain slices and in neonatal animals with in vivo EEG recordings. Consistently, neonatal neurons of CLC-3 knockout mice lack the outward rectifying Cl current and show reduced epileptiform activity upon stimulation. Mechanistically, we demonstrate that activation of CLC-3 Cl channels alters intracellular Cl homeostasis and enhances GABA excitatory activity. Our studies suggest that gluconate can suppress neonatal seizure activities through inhibiting CLC-3 Cl channels in developing brains.
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http://dx.doi.org/10.1186/s13041-019-0465-0 | DOI Listing |
Biochim Biophys Acta Mol Basis Dis
September 2025
Gynecology and Obstetrics, The First Affiliated Hospital of Ningbo University, Ningbo 315000, China. Electronic address:
Cervical cancer is one of the most prevalent types of cancer among women. Nowadays, surgery is still the primary treatment for cervical cancer. Cisplatin was regarded as the standard medication for non-surgical therapy.
View Article and Find Full Text PDFNat Struct Mol Biol
July 2025
Structural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
The trafficking and activity of endosomes relies on the exchange of chloride ions and protons by members of the CLC family of chloride channels and transporters; mutations of the genes encoding these transporters are associated with numerous diseases. Despite their critical roles, the mechanisms by which CLC transporters are regulated are poorly understood. Here we show that two related accessory β-subunits, TMEM9 and TMEM9B, directly interact with ClC-3, ClC-4 and ClC-5.
View Article and Find Full Text PDFBrain
July 2025
Institute of Biological Information Processing, IBI-1, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
CLCN3 and CLCN4 encode the endosomal 2Cl-/H+ exchangers ClC-3 and ClC-4, which are highly expressed within the central nervous system, including hippocampal formation. Pathogenic variants recently found in these genes have given rise to the rare CLCN3- and CLCN4-neurodevelopmental conditions, characterised by a range of neurological and neuropsychiatric complications, such as global developmental delay, intellectual disability as a core feature, seizures, behavioural issues, and brain abnormalities. The mechanisms by which ClC-3 and ClC-4 regulate neuronal function and viability, as well as the molecular pathways affected in CLCN3- and CLCN4-related neurodevelopmental conditions, remain unknown.
View Article and Find Full Text PDFInt Immunopharmacol
May 2025
Department of Pathology and Pathophysiology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. Electronic address:
Polarization of microglia has attracted great attention in ischemic stroke. Emerging evidence suggests that chloride channel 3 (ClC-3) is involved in inflammatory responses and stroke. However, the link between ClC-3 and polarization of microglia in ischemic stroke remains unclear.
View Article and Find Full Text PDFFront Nutr
March 2025
Department of Hematology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Introduction: Certain chloride channels and H/Cl antiporters, such as chloride channel 3 (ClC-3), are expressed at the apical pole of thyrocytes, facilitating iodide (I) efflux. However, the relationship between ClC-3 and I uptake remains unclear. Additionally, whether ClC-3 and reactive oxygen species (ROS) regulate sodium-iodide symporter (NIS) expression and localization under excessive I conditions remain underexplored.
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