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海马体中间神经元通过血清素门控离子通道被激活。

Hippocampal interneurons are excited via serotonin-gated ion channels.

作者信息

McMahon L L, Kauer J A

机构信息

Department of Neurobiology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Neurophysiol. 1997 Nov;78(5):2493-502. doi: 10.1152/jn.1997.78.5.2493.

Abstract

Hippocampal interneurons are excited via serotonin-gated ion channels. J. Neurophysiol. 78: 2493-2502, 1997. Serotonergic neurons of the median raphe nucleus heavily innervate hippocampal GABAergic interneurons located in stratum radiatum of area CA1, suggesting that this strong subcortical projection may modulate interneuron excitability. Using whole cell patch-clamp recording from interneurons in brain slices, we tested the effects of serotonin (5-HT) on the physiological properties of these interneurons. Serotonin produces a rapid inward current that persists when synaptic transmission is blocked by tetrodotoxin and cobalt, and is unaffected by ionotropic glutamate and gamma-aminobutyric acid (GABA) receptor antagonists. The 5-HT-induced current was independent of G-protein activation. Pharmacological evidence indicates that 5-HT directly excites these interneurons through activation of 5-HT3 receptors. At membrane potentials negative to -55 mV, the current-voltage (I-V) relationship of the 5-HT current displays a region of negative slope conductance. Therefore the response of interneurons to 5-HT strongly depends on membrane potential and increases greatly as cells are depolarized. Removal of extracellular calcium, but not magnesium, increases the amplitude of 5-HT-induced currents and removes the region of negative slope conductance, thereby linearizing the I-V relationship. The axons of 5-HT-responsive interneurons ramify widely within CA1; some of these interneurons also project to and arborize extensively in the dentate gyrus. The organization of these inhibitory connections strongly suggests that these cells regulate excitability of both CA1 pyramidal cells and dentate granule cells. As our results indicate that 5-HT may mediate fast excitatory synaptic transmission onto these interneurons, serotonergic inputs can simultaneously modulate the output of both hippocampus and dentate gyrus.

摘要

海马体中间神经元通过5-羟色胺门控离子通道被激活。《神经生理学杂志》78: 2493 - 2502, 1997年。中缝正中核的5-羟色胺能神经元大量支配位于CA1区辐射层的海马体GABA能中间神经元,这表明这种强大的皮层下投射可能调节中间神经元的兴奋性。我们使用脑片中间神经元的全细胞膜片钳记录技术,测试了5-羟色胺(5-HT)对这些中间神经元生理特性的影响。5-羟色胺产生一种快速内向电流,当突触传递被河豚毒素和钴阻断时该电流持续存在,并且不受离子型谷氨酸和γ-氨基丁酸(GABA)受体拮抗剂的影响。5-HT诱导的电流与G蛋白激活无关。药理学证据表明,5-HT通过激活5-HT3受体直接兴奋这些中间神经元。在膜电位负于-55 mV时,5-HT电流的电流-电压(I-V)关系呈现负斜率电导区域。因此,中间神经元对5-HT的反应强烈依赖于膜电位,并且随着细胞去极化而大幅增加。去除细胞外钙而非镁会增加5-HT诱导电流的幅度并消除负斜率电导区域,从而使I-V关系线性化。对5-HT有反应的中间神经元的轴突在CA1区内广泛分支;其中一些中间神经元还投射到齿状回并在其中广泛分支。这些抑制性连接的组织强烈表明这些细胞调节CA1锥体细胞和齿状回颗粒细胞的兴奋性。由于我们的结果表明5-HT可能介导对这些中间神经元的快速兴奋性突触传递,5-羟色胺能输入可以同时调节海马体和齿状回的输出。

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