Effect of endogenous histamine in the ventral hippocampus on fear memory deficits induced by scopolamine as evaluated by step-through avoidance response in rats

In the present study, the effects of endogenous histamine in the ventral hippocampus on fear memory deficits induced by scopolamine were investigated as evaluated by step-through avoidance response in adult male rats. Bilateral ventral hippocampal injection of scopolamine (i.h., 2, 5 μg/site) signif...

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Veröffentlicht in:Physiology & behavior 2006-04, Vol.87 (4), p.687-693
Hauptverfasser: Yu, Chaoyang, Shen, Yao, Xu, Lisha, Zhu, Yuanyuan, Zhuge, Zhenbin, Huang, Yuwen, Henk, Timmerman, Rob, Leurs, Wei, Erqing, Chen, Zhong
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Sprache:eng
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Zusammenfassung:In the present study, the effects of endogenous histamine in the ventral hippocampus on fear memory deficits induced by scopolamine were investigated as evaluated by step-through avoidance response in adult male rats. Bilateral ventral hippocampal injection of scopolamine (i.h., 2, 5 μg/site) significantly produced depressant effects on the active avoidance response in a dose-dependent manner. Histamine H 3-antagonist clobenpropit (5, 10 μg/site) significantly ameliorated the fear memory deficits induced by scopolamine in a dose-dependent manner. Its procognitive effect was completely antagonized by immepip (10 μg/site), a selective histamine H 3-agonist. Both histamine H 1-antagonist pyrilamine and H 2-antagonist cimetidine, also inhibited the procognitive effects of clobenpropit. Additionally, the procognitive effects of clobenpropit on the fear memory deficits induced by scopolamine were significantly potentiated by intraperitoneal (i.p.) injection of histidine, a precursor of histamine, but markedly reversed by i.h. injection of α-fluoromethylhistidine (FMH, 10 μg/site), a selective and potent histidine decarboxylase inhibitor. It is concluded that the increased endogenous histamine release in the ventral hippocampus ameliorates the scopolamine-induced fear memory deficits, and its action is mainly mediated by histamine presynaptic H 3-receptors and postsynaptic H 1- and H 2-receptors.
ISSN:0031-9384
1873-507X
DOI:10.1016/j.physbeh.2006.01.004