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内源性组胺在行走过程中促进海马体的长时程增强。

Endogenous histamine facilitates long-term potentiation in the hippocampus during walking.

机构信息

Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada.

出版信息

J Neurosci. 2010 Jun 9;30(23):7845-52. doi: 10.1523/JNEUROSCI.1127-10.2010.

Abstract

Long-term potentiation (LTP) in hippocampal CA1 depends on the behavioral state of LTP induction. We hypothesize that histaminergic activity in the septohippocampal system, which is active during walking compared with other behavioral states, is responsible for the behavioral dependence of LTP. Field basal-dendritic EPSPs of CA1 pyramidal cells were recorded in freely behaving rats, and LTP was induced by a single 200 Hz stimulation train (0.5 s duration). Basal-dendritic LTP was facilitated when induced during walking compared with awake immobility (IMM) or rapid-eye-movement sleep. The facilitation of basal-dendritic LTP during walking was abolished by lesion of tuberomammillary nucleus (TMN) neurons with orexin-saporin or by intramedial-septal infusion of the H(1) histaminergic blocker triprolidine but not the H(2) histaminergic blocker cimetidine. Conversely, histamine infusion in the medial septum enhanced the basal-dendritic LTP induced during IMM to a magnitude similar to that induced during walking. Basal-dendritic LTP induced during walking was not further enhanced by intraseptal histamine infusion. Combined with the previous result that behavior-dependent LTP is mediated by cholinergic septohippocampal neurons, we conclude that the facilitation of basal-dendritic LTP in CA1 during walking was mediated by TMN histaminergic afferents acting on H(1) receptors in the medial septum, which may then enhance cholinergic and noncholinergic inputs to the hippocampus.

摘要

长时程增强(LTP)在海马 CA1 区依赖于 LTP 诱导的行为状态。我们假设,与其他行为状态相比,在行走期间活跃的隔海马系统中的组胺能活性是 LTP 行为依赖性的原因。在自由活动的大鼠中记录 CA1 锥体神经元的基底树突 EPSP,并通过单次 200 Hz 刺激(0.5 s 持续时间)诱导 LTP。与清醒不动(IMM)或快速眼动睡眠相比,在行走期间诱导时基底树突 LTP 得到促进。用 orexin-saporin 损伤结节乳头核(TMN)神经元或用 H(1)组胺能阻滞剂三普洛吡啶而非 H(2)组胺能阻滞剂西咪替丁在中隔内输注可消除行走时基底树突 LTP 的促进作用。相反,在中隔内输注组胺增强了在 IMM 期间诱导的基底树突 LTP,其幅度与在行走期间诱导的相似。在行走期间,在中隔内给予组胺不能进一步增强基底树突 LTP。结合先前的结果,即行为依赖性 LTP 由胆碱能隔海马神经元介导,我们得出结论,行走时 CA1 中基底树突 LTP 的促进作用是由 TMN 组胺能传入纤维通过作用于中隔内的 H(1)受体介导的,这可能增强海马的胆碱能和非胆碱能传入。

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