## Abstract The aim of the present study was to find out if a cell line of glial origin possesses sigma and/or phencyclidine (PCP) binding sites. Binding of [^3^H]1,3‐di‐o‐tolyl‐guanidine (DTG), a highly selective ligand for sigma binding sites, and of [^3^H]N‐[1‐(2‐thienyl)cyclohexyl] piperidine (
[3H]spiperone binding sites in rat primary glial cultures, C6 glioma, and B104 neuroblastoma
✍ Scribed by J. A. Severson; J. S. de Vellis; C. E. Finch
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 333 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0360-4012
No coin nor oath required. For personal study only.
✦ Synopsis
Binding sites for [iH]spiperone were detected on membranes from primary glial cultures from neonatal rat cortex and striatum and from the C6 glioma cells.
['HISpiperone binding was displacable by d-butaclamol. However, competition studies suggest that ['Hlspiperone binding to primary glial cultures was mainly to serotonergic sites, and binding to the C6 glioma was alpha-adrenergic. No specific binding was detected to membranes from B 104 neuroblastoma cells. Although [?H]spiperone binding to glial sites on whole striatum under generally used conditions is small (about lo%), the striatal glial hyperactivity that is often associated with neuronal degeneration could lead to an overestimation of presumed neuronal binding sites for dopaminergic ligands.
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