Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518791PMC
http://dx.doi.org/10.1186/s13041-019-0465-0DOI Listing

Publication Analysis

Top Keywords

clc-3 channels
16
developing brains
12
inhibiting clc-3
12
seizure activity
8
clc-3 chloride
8
chloride channels
8
gluconate inhibits
8
neonatal seizure
8
outward rectifying
8
rectifying current
8

Similar Publications

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 PDF

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 PDF

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 PDF

ClC-3-depedent polarization of microglia protects against cerebral ischemic injury in mice.

Int 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 PDF

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.

View Article and Find Full Text PDF