期刊
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
卷 67, 期 1, 页码 145-150出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0091-3057(00)00320-8
关键词
anxiety; cimetidine; compound 48/80; histamine receptors; light/dark test; mepyramine; thioperamide
Experimental anxiety in mice was evaluated using a light/dark test at 60 min after injection of various histaminergics. Thioperamide, a histamine H-3 receptor inhibitor (5-20 mg/kg, intraperitoneal [IPI), Compound 48/80, a mast cell degranulator (0.1-10 mug/2 mul, intracerebroventricularly [ICV]), mepyramine, a histamine H-1 receptor antagonist (0.1-10 mug/2 mul, ICV) or cimetidine, a histamine Hz receptor antagonist (0.1 - 10 mug/2 mul, ICV) alone did not affect the locomotive activity, the time spent in the light zone, and number of shuttle crossings in the light/clark test. However, the time spent in the light zone and the number of shuttle crossings significantly decreased only when cimetidine (0.1-10 mug/2 mul, ICV) was co-treated with either thioperamide (10 mg/10 ml/kg, IF) or Compound 48/80 (1.0 mug/2 mul, ICV). The decrease in these behavioral parameters suggests induced experimental anxiety in mice. The experimental anxiety was antagonized by mepyramine (10 mug/2 CL1, ICV). These results suggest that not only neuronal histamine release induced by thioperamide but also nonneuronal (mast cells) histamine release induced by Compound 48/80 play an important role in inducing experimental anxiety via postsynaptic H1 and H-2 receptors. In addition, it is likely that the anxiety may be mediated by the stimulation of H-1 receptors, while H-2 receptors may inhibit the anxiety produced by the activation of H-1 receptors. (C) 2000 Elsevier Science Inc. All rights reserved.
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