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Acute modulation of the cholinergic system in the mouse brain detected by pharmacological resting-state functional MRI

机译:药理学静息态功能MRI检测到的小鼠大脑胆碱能系统的急性调节

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Introduction: The cholinergic system is involved in learning and memory and is affected in neurodegenerative disorders such as Alzheimer's disease. The possibility of non-invasively detecting alterations of neurotransmitter systems in the mouse brain would greatly improve early diagnosis and treatment strategies. The hypothesis of this study is that acute modulation of the cholinergic system might be reflected as altered functional connectivity (FC) and can be measured using pharmacological resting-state functional MRI (rsfMRI). Material and methods: Pharmacological rsfMRI was performed on a 9.4 T MRI scanner (Bruker BioSpec, Germany) using a gradient echo EPI sequence. All mice were sedated with medetomidine. C57BL/6 mice (N = 15/group) were injected with either saline, the cholinergic antagonist scopolamine, or methyl-scopolamine, after which rsfMRI was acquired. For an additional group (N = 8), rsfMRI scans of the same mouse were acquired first at baseline, then after the administration of scopolamine and finally after the additional injection of the cholinergic agonist milameline. Contextual memory was evaluated with the same setup as the pharmacological rsfMRI using the passive avoidance behavior test. Results: Scopolamine induced a dose-dependent decrease of FC between brain regions involved in memory. Scopolamine-induced FC deficits could be recovered completely by milameline for FC between the hippocampus-thalamus, cingulate-retrosplenial, and visual-retrosplenial cortex. FC between the cingulate-rhinal, cingulate-visual and visual-rhinal cortex could not be completely recovered by milameline. This is consistent with the behavioral outcome, where milameline only partially recovered scopolamine-induced contextual memory deficits. Methyl-scopolamine administered at the same dose as scopolamine did not affect FC in the brain. Conclusion: The results of the current study are important for future studies in mouse models of neurodegenerative disorders, where pharmacological rsfMRI may possibly be used as a non-invasive read-out tool to detect alterations of neurotransmitter systems induced by pathology or treatment. (C) 2015 The Authors. Published by Elsevier Inc.
机译:简介:胆碱能系统参与学习和记忆,并受神经退行性疾病(例如阿尔茨海默氏病)的影响。非侵入性检测小鼠大脑中神经递质系统变化的可能性将大大改善早期诊断和治疗策略。这项研究的假设是胆碱能系统的急性调节可能反映为功能连接性(FC)的改变,并且可以使用药理静息状态功能MRI(rsfMRI)进行测量。材料和方法:药理学rsfMRI使用梯度回波EPI序列在9.4 T MRI扫描仪(Bruker BioSpec,德国)上进行。用美托咪定对所有小鼠进行镇静。给C57BL / 6小鼠(N = 15 /组)注射生理盐水,胆碱能拮抗剂东pol碱或甲基东sco碱,然后进行rsfMRI检查。对于另一组(N = 8),首先在基线时获取同一只小鼠的rsfMRI扫描图,然后在使用东pol碱后,再额外注射胆碱能激动剂米拉美林后,进行rsfMRI扫描。使用被动回避行为测试,以与药理学rsfMRI相同的设置评估语境记忆。结果:东co碱诱导记忆相关的大脑区域之间FC的剂量依赖性降低。 co胺对海马-丘脑,扣带回-脾小肌和视觉-脾小肌皮质之间的FC可以完全弥补recovered胺引起的FC缺陷。密拉美林不能完全恢复扣带回-皮层,扣带回-皮层和FC-之间。这与行为结果一致,米拉美林仅部分恢复了东pol碱引起的情境记忆缺陷。与东pol碱相同剂量的甲基东sco碱不会影响大脑中的FC。结论:本研究的结果对神经退行性疾病小鼠模型的未来研究非常重要,在该模型中,药理学rsfMRI可能被用作非侵入性读出工具,以检测由病理或治疗引起的神经递质系统的变化。 (C)2015作者。由Elsevier Inc.发布

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