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海马体内的紧张性抑制影响福尔马林疼痛诱导的锥体细胞抑制,但不影响大鼠背侧CA1区的兴奋。

Intra-hippocampal tonic inhibition influences formalin pain-induced pyramidal cell suppression, but not excitation in dorsal field CA1 of rat.

作者信息

Zheng F, Khanna S

机构信息

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Blk MD9, 2 Medical Drive, Singapore 117597, Singapore.

出版信息

Brain Res Bull. 2008 Dec 16;77(6):374-81. doi: 10.1016/j.brainresbull.2008.09.004. Epub 2008 Oct 11.

Abstract

It has been hypothesized that intra-hippocampal GABAergic inhibitory interneurons mediate formalin pain-induced suppression of dorsal hippocampal CA1 pyramidal cell discharge. The present study performed on anaesthetized rats tested the hypothesis by disrupting GABAergic mechanisms with intra-hippocampal administration of the GABA(A) receptor antagonist bicuculline methiodide, applied either dorsally into the pyramidal cell layer and stratum oriens (dorsal-bicuculline) or ventrally into the region of apical dendrites (ventral-bicuculline). It was found that ventral-, but not dorsal-bicuculline attenuated formalin-induced suppression of pyramidal cell extracellular discharge. The antagonism was selective in such a way that the excitation of pyramidal cell was unaffected. Interestingly, ventral-bicuculline strongly disinhibited CA1 pyramidal cells and shifted the distribution of their spontaneous discharge to values higher than the control group. However, dorsal-bicuculline disinhibited the local CA1 interneurons that were strongly excited on injection of formalin. Overall, the findings favour the notion that tonic GABA(A) receptor mechanisms located in the region of apical dendrites facilitate formalin-induced pyramidal cell suppression by masking the background excitatory drive impinging on the pyramidal cells. Interestingly, both the attenuation of formalin-induced inhibition and facilitation of basal discharge of CA1 pyramidal cells by ventral-bicuculline are similar to the effects seen previously with the destruction of medial septal cholinergic neurons. This convergence of effects strengthens the proposal that the network of medial septal cholinergic neurons and hippocampal GABAergic interneurons influence formalin pain-induced CA1 pyramidal cell suppression. In addition, the data point to a non-overlapping excitatory drive whose strength is unaffected by the inhibitory drive that underpins formalin suppression.

摘要

有假说认为,海马体内的γ-氨基丁酸(GABA)能抑制性中间神经元介导了福尔马林疼痛诱导的背侧海马CA1锥体细胞放电抑制。本研究在麻醉大鼠身上进行,通过海马内注射GABA(A)受体拮抗剂甲硫酸荷包牡丹碱来破坏GABA能机制,从而验证这一假说。甲硫酸荷包牡丹碱分别背侧注入锥体细胞层和原层(背侧-荷包牡丹碱)或腹侧注入顶端树突区域(腹侧-荷包牡丹碱)。结果发现,腹侧而非背侧的荷包牡丹碱减弱了福尔马林诱导的锥体细胞胞外放电抑制。这种拮抗作用具有选择性,即锥体细胞的兴奋不受影响。有趣的是,腹侧-荷包牡丹碱强烈地解除了对CA1锥体细胞的抑制,并将其自发放电分布转移到高于对照组的值。然而,背侧-荷包牡丹碱解除了局部CA1中间神经元的抑制,这些中间神经元在注射福尔马林时会强烈兴奋。总体而言,这些发现支持这样一种观点,即位于顶端树突区域的持续性GABA(A)受体机制通过掩盖作用于锥体细胞的背景兴奋性驱动,促进了福尔马林诱导的锥体细胞抑制。有趣的是,腹侧-荷包牡丹碱对福尔马林诱导的抑制的减弱以及对CA1锥体细胞基础放电的促进,都与之前内侧隔区胆碱能神经元破坏时所观察到的效应相似。这些效应的趋同强化了这样一种观点,即内侧隔区胆碱能神经元网络和海马GABA能中间神经元影响福尔马林疼痛诱导的CA1锥体细胞抑制。此外,数据表明存在一种不重叠的兴奋性驱动,其强度不受支撑福尔马林抑制的抑制性驱动的影响。

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