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Muscarinic antagonist binding site heterogeneity as evidenced by autoradiography after direct labeling with [3H]-QNB and [3H]-pirenzepine
Authors:J K Wamsley  D R Gehlert  W R Roeske  H I Yamamura
Institution:1. Departments of Psychiatry, Anatomy and Pharmacology University of Utah School of Medicine, Salt Lake City, Utah 84132, USA;2. Departments of Pharmacology, Biochemistry, Psychiatry, Internal Medicine University of Arizona Health Sciences Center, Tucson, Arizona 85724, USA;1. Arizona Research Laboratories University of Arizona Health Sciences Center, Tucson, Arizona 85724, USA
Abstract:Saturable, high affinity binding of tritiated pirenzepine ( 3H]-PZ) was obtained in slide mounted tissue sections prior to performing autoradiographic localization of these binding sites. The binding in tissue sections of rostral rat forebrain gave a KD of 18nM and a Bmax of 51 fmoles/mg tissue. These binding characteristics are similar to those previously obtained in homogenate membrane preparations and indicate the binding is taking place in a similar manner. The distribution of the binding sites labeled with 3H]-PZ represented a subpopulation of those which could be labeled with tritiated quinuclidinyl benzilate ( 3H]-QNB). Thus, 3H]-PZ and 3H]-QNB both label regions of the cerebral cortex, hippocampus, striatum and dorsal horn of the spinal cord, while sites in the cerebellum, nucleus tractus solitarius, facial nucleus and ventral horn of the spinal cord are labeled with 3H]-QNB and not by 3H]-PZ. These observations indicate separate regions of the brain where antagonists bind to subtypes of muscarinic receptors.
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