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1 Institute of Neurobiology and Institute of Clinical Neuroscience, Göteborg University, Göteborg, Sweden; and 2 Neuropharmacologie, Institut National de la Santé et de la Recherche Médicale U114, Collège de France, Paris, France
Astrocytes represent a major target for endothelins (ETs), a family of peptides that have potent and multiple effects on signal transduction pathways and can be released by several cell types in the brain. In the present study we have investigated the involvement of different ET receptor subtypes on intercellular dye diffusion, intracellular Ca2+ homeostasis, and intercellular Ca2+ signaling in cultured rat astrocytes from hippocampus and striatum. Depending on the ET concentration and the receptor involved, ET-1- and ET-3-induced intracellular Ca2+ increases with different response patterns. Both ET-1 and ET-3 are powerful inhibitors of gap junctional permeability and intercellular Ca2+ signaling. The nonselective ET receptor agonist sarafotoxin S6b and the ETB receptor-selective agonist IRL 1620 mimicked these inhibitions. The ET-3 effects were only marginally affected by an ETA receptor antagonist but completely blocked by an ETB receptor antagonist. However, the ET-1-induced inhibition of gap junctional dye transfer and intercellular Ca2+ signaling was only marginally blocked by ETA or ETB receptor-selective antagonists but fully prevented when these antagonists were applied together. The ET-induced inhibition of gap junction permeability and intercellular Ca2+ signaling indicates that important changes in the function of astroglial communication might occur when the level of ETs in the brain is increased.
endothelins; cultured astrocytes; gap junctions; calcium waves
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