通过对神经和血液动力学信号的宽视场光学绘图研究急性应激对诱发皮层连接性的影响

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Hayeon Kim, Haebin Jeong, Jiyoung Lee, Jaeseung Yei, Minah Suh
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引用次数: 0

摘要

单次暴露于应激可诱发神经元的功能变化,从而可能导致急性应激障碍或创伤后应激障碍。在这项研究中,我们利用体内宽视场光学映射同时测量了整个皮层区域的神经钙信号和血液动力学反应。我们发现,在急性应激条件下,大脑皮层对胡须刺激的映射发生了改变。特别是,相对于躯体感觉皮层的桶状场(S1BF),前部皮层(初级/次级运动、躯体感觉前肢皮层)的胼胝体投射减弱了。相反,后部皮层相对于 S1BF 的投射大部分保持不变或偶尔增强。此外,皮层内连接的变化与皮层间连接的变化相反。因此,S1BF 与前部皮层的连接加强了,而与后部皮层的连接却减弱了。这表明,众所周知的桶状皮层投射路线得到了加强。总之,我们的活体广域光学绘图研究表明,一次急性应激可影响整个大脑网络,同时影响神经和血液动力学反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effects of Acute Stress on Evoked-cortical Connectivity through Wide-field Optical Mapping of Neural and Hemodynamic Signals.

A single exposure to stress can induce functional changes in neurons, potentially leading to acute stress disorder or post-traumatic stress disorder. In this study, we used in vivo wide-field optical mapping to simultaneously measure neural calcium signals and hemodynamic responses over the whole cortical area. We found that cortical mapping to whisker stimuli was altered under acute stress conditions. In particular, callosal projections in the anterior cortex (primary/secondary motor, somatosensory forelimb cortex) relative to barrel field (S1BF) of somatosensory cortex were weakened. On the contrary, the projections in posterior cortex relative to S1BF were mostly unchanged or were only occasionally strengthened. In addition, changes in intra-cortical connection were opposite to those in inter-cortical connection. Thus, the S1BF connections to the anterior cortex were strengthened while those to the posterior cortex were weakened. This suggests that the well-known barrel cortex projection route was enhanced. In summary, our in vivo wide-field optical mapping study indicates that a single acute stress can impact whole-brain networks, affecting both neural and hemodynamic responses.

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来源期刊
Experimental Neurobiology
Experimental Neurobiology Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.30
自引率
4.20%
发文量
29
期刊介绍: Experimental Neurobiology is an international forum for interdisciplinary investigations of the nervous system. The journal aims to publish papers that present novel observations in all fields of neuroscience, encompassing cellular & molecular neuroscience, development/differentiation/plasticity, neurobiology of disease, systems/cognitive/behavioral neuroscience, drug development & industrial application, brain-machine interface, methodologies/tools, and clinical neuroscience. It should be of interest to a broad scientific audience working on the biochemical, molecular biological, cell biological, pharmacological, physiological, psychophysical, clinical, anatomical, cognitive, and biotechnological aspects of neuroscience. The journal publishes both original research articles and review articles. Experimental Neurobiology is an open access, peer-reviewed online journal. The journal is published jointly by The Korean Society for Brain and Neural Sciences & The Korean Society for Neurodegenerative Disease.
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