胆碱能基底前脑神经元调节血管动力学和脑脊液通量

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Kai-Hsiang Chuang, Xiaoqing Alice Zhou, Ying Xia, Zengmin Li, Lei Qian, Eamonn Eeles, Grace Ngiam, Jurgen Fripp, Elizabeth J. Coulson
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引用次数: 0

摘要

脑废物通过脑脊液(CSF)途径清除,即淋巴系统,其功能障碍可能是许多脑部疾病的基础。先前的研究表明,通过血氧水平依赖(BOLD)功能磁共振成像(fMRI)测量的相干血管振荡与脑脊液流入相结合,驱动流体通量。然而,这种耦合是如何调节的,它是否介导废物清除,以及它为什么受到损害仍然不清楚。在这里,我们证明胆碱能神经元调节BOLD-CSF偶联和淋巴功能。我们发现BOLD-CSF偶联与老年人皮质胆碱能活性相关。雌性小鼠基底前脑胆碱能神经元的损伤损害了淋巴外排和相关的BOLD-CSF偶联、动脉搏动和淋巴内流的变化。乙酰胆碱酯酶抑制剂主要通过外周机制改变这些动力学。我们的研究结果表明,胆碱能损失通过神经血管机制损害淋巴功能,可能导致病理性废物积累。这可能为开发淋巴功能障碍的诊断和治疗提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cholinergic basal forebrain neurons regulate vascular dynamics and cerebrospinal fluid flux

Cholinergic basal forebrain neurons regulate vascular dynamics and cerebrospinal fluid flux

Brain waste is cleared via a cerebrospinal fluid (CSF) pathway, the glymphatic system, whose dysfunction may underlie many brain conditions. Previous studies show coherent vascular oscillation, measured by blood oxygenation level-dependent (BOLD) fMRI, couples with CSF inflow to drive fluid flux. Yet, how this coupling is regulated, whether it mediates waste clearance, and why it is impaired remain unclear. Here we demonstrate that cholinergic neurons modulate BOLD-CSF coupling and glymphatic function. We find BOLD-CSF coupling correlates cortical cholinergic activity in aged humans. Lesioning basal forebrain cholinergic neurons in female mice impairs glymphatic efflux and associated changes in BOLD-CSF coupling, arterial pulsation and glymphatic influx. An acetylcholinesterase inhibitor alters these dynamics, primarily through peripheral mechanisms. Our results suggest cholinergic loss impairs glymphatic function by a neurovascular mechanism, potentially contributing to pathological waste accumulation. This may provide a basis for developing diagnostics and treatments for glymphatic dysfunction.

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来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
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