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Tricyclic antidepressant desipramine induces stereospecific opiate binding and lipid modifications in rat glioma C6 cells
Authors:S Albouz  B Tocqué  JJ Hauw  JM Boutry  F Le Saux  R Bourdon  N Baumann
Institution:1. INSERM U.134, Laboratoire de Neurochimie, Hôpital Fernand-Widal, Paris, France;2. Laboratoire de Neuropathologie Charles Foix, Hôpital de la Salpêtrière Hôpital Fernand-Widal, Paris, France;3. Laboratoire de Biochimie- Toxicologie, Hôpital Fernand-Widal, Paris, France
Abstract:Incubation for 48 hours of C6 glioma cell cultures with 10?4M tricyclic antidepressant desipramine gave rise to a quantitative increase of total lipids and to qualitative modifications of glycosphingolipids involving detection by thin-layer chromatography of spots migrating according to cerebroside and sulfatide and presence of an abnormal ganglioside pattern. These lipid modifications were associated with the appearance of stereospecific binding of opiates (dihydromorphine) with a dissociation constant of 30–60 nM. These results favor an important role of lipids in opioid receptor function.
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