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首页> 外文期刊>Brain research bulletin >Arginine vasopressin attenuates dysfunction of hippocampal theta and gamma oscillations in chronic cerebral hypoperfusion via V1a receptor
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Arginine vasopressin attenuates dysfunction of hippocampal theta and gamma oscillations in chronic cerebral hypoperfusion via V1a receptor

机译:Aginine vasopressin通过V1A受体衰减慢性脑低渗和慢性脑低血灌注中的海马θ和γ振荡的功能障碍

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Chronic cerebral hypoperfusion (CCH) is associated with cognitive decline in aging, Alzheimer's disease and vascular dementia. Neural oscillations and their interactions support brain communication and involve in cognitive function. Although arginine vasopressin (AVP) has been linked to spatial learning and memory, the effects of AVP on CCH in terms of the hippocampal neural network is unknown. Here we investigated the dynamics of neural oscillations in the hippocampus in a rat model of permanent bilateral carotid arteries occlusion (two-vessel occlusion, 2VO) under urethane-anesthesia. Hypertonic saline (5.3%) was injected intraperitoneally to induce the endogenous AVP, and SR49059 was used as V1a receptor (an AVP receptor) antagonist. The results showed that AVP partly changed CA3 Schaffer collateral (CA3-SC) power distribution in the rat model of 2VO via V1a receptor, increased theta synchrony between CA3-SC and CA1 areas, enhanced. CA3-SC theta-middle gamma phase-phase coupling, and improved spatial learning and memory performance. Biochemical fractionation further confirmed the recovery effect on N-methyl-D-aspartate receptor subunit 2B (NR2B) and postsynaptic density protein 95 (PSD-95) surface expressions after hypertonic saline injection, suggesting a possible molecular mechanism in the hippocampus. The findings shed light on a functional role of endogenous AVP from a neural network perspective that AVP improves theta synchronization and accurate coordination of theta-gamma coupling probably through upregulating NR2B and PSD-95 expressions, and further promotes neural communication in the hippocampus to some extent. As a result, the impairment of spatial learning and memory induced by CCH is significantly alleviated.
机译:慢性脑低渗(CCH)与老龄化,阿尔茨海默病和血管痴呆的认知下降有关。神经振荡及其相互作用支持大脑通信并涉及认知功能。虽然精氨酸血管加压素(AVP)已与空间学习和记忆相关联,但AVP在海马神经网络方面的CCH的影响是未知的。在这里,我们研究了在氨基甲酸酯麻醉下的永久性双侧颈动脉闭塞(两血管闭塞,2VO)大鼠模型中神经振荡中的神经振荡动态。高渗盐水(5.3%)腹膜内注射以诱导内源性AVP,SR49059用作V1A受体(AVP受体)拮抗剂。结果表明,AVP通过V1A受体进行了大鼠2VO大鼠模型中的Ca3 Schafer抵押品(CA3-SC)功率分布,增加了Ca3-SC和CA1区域之间的Theta同步,增强。 CA3-SCθ-中间伽马相位耦合,以及改善的空间学习和内存性能。生物化学分级进一步证实了高渗盐水注射后对N-甲基-D-天冬氨酸受体亚基2B(NR2B)和突触后密度蛋白质95(PSD-95)表面表达的回收效果,表达了海马可能的分子机制。从神经网络角度来看,AVP可能通过上调NR2B和PSD-95表达,AVP改善了AVP的内源性AVP的功能作用,提高了Theta-Gamma偶联的同步和精确协调,并在一定程度上进一步促进海马中的神经通信。结果,CCH引起的空间学习和记忆的减值显着减轻了。

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