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Guanosine 5′-(γ-[35S]Thio)triphosphate Autoradiography Allows Selective Detection of Histamine H3 Receptor-Dependent G Protein Activation in Rat Brain Tissue Sections
Authors:Jarmo T Laitinen  Marianne Jokinen
Abstract:Abstract: Histamine elicits its biological effects via three distinct G protein-coupled receptors, termed H1, H2, and H3. We have used guanosine 5′-(γ-35S]thio)triphosphate (GTPγ35S]) autoradiography to localize histamine receptor-dependent G protein activation in rat brain tissue sections. Initial studies revealed that in basal conditions, adenosine was present in tissue sections in sufficient concentrations to generate an adenosine A1 receptor-dependent GTPγ35S] signal in several brain regions. All further incubations therefore contained 8-cyclopentyl-1,3-dipropylxanthine (10 µM), a selective A1 receptor antagonist. Histamine elicited dose-dependent increments in GTPγ35S] binding to discrete anatomical structures, most notably the caudate putamen, cerebral cortex, and substantia nigra. The overall anatomical pattern of the histamine-evoked binding response closely reflects the known distribution of H3 binding sites and was faithfully mimicked by Nα-methylhistamine, (R)-α-methylhistamine, and immepip, three H3-selective agonists. In all regions examined, the GTPγ35S] signal was reversed with thioperamide and clobenpropit, two potent H3-selective antagonists, whereas mepyramine, a specific H1 antagonist, and cimetidine, a prototypic H2 antagonist, proved ineffective. These data indicate that in rat brain tissue sections, GTPγ35S] autoradiography selectively detects H3 receptor-dependent signaling in response to histamine stimulation. As the existing evidence suggests that GTPγ35S] autoradiography preferentially reveals responses to Gi/o-coupled receptors, our data indicate that most, if not all, central H3 binding sites represent functional receptors coupling to Gi/o, the inhibitory class of G proteins. Besides allowing more detailed studies on H3 receptor signaling within anatomically restricted regions of the CNS, GTPγ35S] autoradiography offers a novel approach for functional in vitro screening of H3 ligands.
Keywords:Adenosine A1 receptors  Autoradiography  Basal ganglia  Histamine H3 receptors  Receptor-G protein coupling  Substantia nigra
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