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在乳头体上区微量注射卡巴胆碱可抑制CA1锥体细胞的突触兴奋性。

Microinjection of carbachol in the supramammillary region suppresses CA1 pyramidal cell synaptic excitability.

作者信息

Jiang Fengli, Khanna Sanjay

机构信息

Department of Physiology (MD9), Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

出版信息

Hippocampus. 2006;16(10):891-905. doi: 10.1002/hipo.20219.

Abstract

Previous studies have established that the posterior hypothalamus-supramammillary (SUM) region is involved in the control of the hippocampal theta rhythm and also modulates the synaptic excitation of hippocampal neurons. Particularly, the medial but not lateral SUM region mediates reticular stimulation-induced suppression of CA1 pyramidal cell synaptic excitation to Schaffer collateral stimulation. In the present study using urethane anesthetized rats, we have investigated the effect of direct chemical stimulation of the posterior hypothalamus-SUM region on CA1 pyramidal cell excitability. It was observed that microinjection of the cholinergic muscarinic receptor agonist, carbachol (0.1 microl, concentration of either 0.0052, 0.156, or 0.625 microg/microl), evoked concentration-dependent suppression of CA1 pyramidal cell excitability that was dissociated from theta activation. Further, carbachol microinjection preferentially recruited the lateral SUM region when compared with the medial SUM and the posterior hypothalamic regions. In this context, the shortest latencies to suppression at the lowest concentration of carbachol and the strongest suppression at higher concentrations were observed with lateral microinjections. The carbachol-induced suppression was attenuated by inactivation of the medial septal region by microinjection of procaine (0.5 microl, 20% w/v). These results underscore a possible role for cholinergic mechanisms in the lateral SUM region in modulation of CA1 pyramidal cell synaptic excitation via the medial septal region. Furthermore, the present findings when juxtaposed with the medial SUM mediation of reticularly-elicited suppression suggest a medial-lateral topographic organization of the SUM region in modulation of CA1 excitability.

摘要

以往的研究已经证实,下丘脑后部-乳头体上核(SUM)区域参与海马θ节律的控制,并且还调节海马神经元的突触兴奋性。特别地,SUM区域的内侧而非外侧介导网状刺激诱导的对CA1锥体细胞对沙氏侧支刺激的突触兴奋性的抑制。在本研究中,我们使用乌拉坦麻醉的大鼠,研究了直接化学刺激下丘脑后部-SUM区域对CA1锥体细胞兴奋性的影响。我们观察到,微量注射胆碱能毒蕈碱受体激动剂卡巴胆碱(0.1微升,浓度分别为0.0052、0.156或0.625微克/微升),可引起与θ激活无关的CA1锥体细胞兴奋性的浓度依赖性抑制。此外,与内侧SUM和下丘脑后部区域相比,微量注射卡巴胆碱优先激活外侧SUM区域。在这种情况下,外侧微量注射在最低浓度卡巴胆碱时观察到抑制的最短潜伏期,在较高浓度时观察到最强的抑制。通过微量注射普鲁卡因(0.5微升,20% w/v)使内侧隔区失活,可减弱卡巴胆碱诱导的抑制。这些结果强调了外侧SUM区域胆碱能机制通过内侧隔区调节CA1锥体细胞突触兴奋性的可能作用。此外,本研究结果与内侧SUM介导的网状刺激诱导的抑制相结合,提示SUM区域在内侧-外侧拓扑组织中对CA1兴奋性的调节作用。

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