Pregnenolone sulfate activates NMDA receptor channels
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24359434
DOI
10.33549/physiolres.932558
PII: 932558
Knihovny.cz E-resources
- MeSH
- Ion Channel Gating physiology MeSH
- HEK293 Cells MeSH
- Humans MeSH
- Pregnenolone metabolism MeSH
- Receptors, N-Methyl-D-Aspartate metabolism MeSH
- Calcium metabolism MeSH
- Calcium Signaling physiology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Pregnenolone MeSH
- pregnenolone sulfate MeSH Browser
- Receptors, N-Methyl-D-Aspartate MeSH
- Calcium MeSH
Pregnenolone sulfate (PS), an endogenously occurring neurosteroid, has been shown to modulate the activity of several neurotransmitter-gated channels, including the NMDA receptor (NMDAR). NMDARs are glutamate-gated ion channels involved in excitatory synaptic transmission, synaptic plasticity, and excitotoxicity. In this study, we analyzed the effects of PS on calcium signaling in cultured hippocampal neurons and HEK293 cells expressing NMDAR. The cells were loaded with the Ca(2+) sensor Fura-2. In agreement with previous electrophysiological experiments, PS potentiated the increases in intracellular Ca(2+) induced by an exogenous application of glutamate; however, PS also increased intracellular Ca(2+) in the absence of exogenous NMDA agonist. The agonist-independent effect of PS was induced in all neurons studied and in HEK293 cells expressing GluN1/GluN2A-B receptors in a neurosteroid-specific manner. We conclude that PS is an endogenous NMDA agonist that activates the GluN1/GluN2A-B receptors.
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