Volume 363, Issue 4 pp. 517-531
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Adenosine A1 receptors are located predominantly on axons in the rat hippocampal formation

Thomas H. Swanson M. D.

Corresponding Author

Thomas H. Swanson M. D.

Department of Neurology, The Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195

Department of Neuroscience Research, The Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195

NC3–163, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44129Search for more papers by this author
Judith A. Drazba

Judith A. Drazba

Department of Neuroscience Research, The Research Institute, The Cleveland Clinic Foundation, Cleveland, Ohio 44195

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Scott A. Rivkees

Scott A. Rivkees

Wells Center for Pediatric Research, Departments of Pediatric Endocrinology, Biochemistry, Molecular Biology, and Neurobiology, Riley Hospital, Indiana University, Indianapolis, Indiana 46202–5225

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First published: 25 December 1995
Citations: 72

Abstract

The nucleoside adenosine exerts potent biological effects via specific receptors, including the inhibitory Al adenosine receptor (A1AR). In the hippocampus A1ARs play an important role in regulating neuronal activity. However, the cellular sites of hippocampal A1ARs are undefined. Using in situ hybridization, receptor autoradiography, and single- and double-label immunocytochemistry techniques, we have characterized the cellular sites of A1AR expression in the rat hippocampus. In situ hybridization and receptor autoradiography studies revealed strikingly different patterns of labeling. In situ hybridization studies revealed heaviest labeling of cell bodies in the granular layer of the dentate gyrus and the pyramidal layers of Ammon's horn. In contrast, using [3H] we observed heavy specific labeling over the neuropil in the dentate hilus stratum moleculare, stratum lacunosum-inoleculare, stratum radiatum, and stratum oriens, and little labeling over cell bodies. Using single-label immunocytochemistry, A1AR immunoreactivity was found to be heaviest over fibers in regions corresponding with heavy [3H] labeling. Double-label florescent confocal microscopy was then used to determine the identity of labeled fibers. A1AR immunoreactivity was found to co-localize with SMI-31 that labels axons, but not with MAP2a, b that labels cell bodies and dendrites, orwith synaptophysin that labels synapses. These data identify axons as the predominant site of A1AR expression in hippocampus. Activation of A1ARs may be a powerful mechanism by which adenosine alters axonal transmission to inhibit neurotransmitter release. © 1995 Wiley-Liss, Inc.

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