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用于计算脑成像的多模光纤内窥镜。

Multimode fiber endoscopes for computational brain imaging.

作者信息

Amitonova Lyubov V

机构信息

Vrije Universiteit Amsterdam, Department of Physics and Astronomy, Amsterdam, The Netherlands.

Advanced Research Center for Nanolithography, Amsterdam, The Netherlands.

出版信息

Neurophotonics. 2024 Sep;11(Suppl 1):S11509. doi: 10.1117/1.NPh.11.S1.S11509. Epub 2024 Mar 6.

Abstract

Advances in imaging tools have always been a pivotal driver for new discoveries in neuroscience. An ability to visualize neurons and subcellular structures deep within the brain of a freely behaving animal is integral to our understanding of the relationship between neural activity and higher cognitive functions. However, fast high-resolution imaging is limited to sub-surface brain regions and generally requires head fixation of the animal under the microscope. Developing new approaches to address these challenges is critical. The last decades have seen rapid progress in minimally invasive endo-microscopy techniques based on bare optical fibers. A single multimode fiber can be used to penetrate deep into the brain without causing significant damage to the overlying structures and provide high-resolution imaging. Here, we discuss how the full potential of high-speed super-resolution fiber endoscopy can be realized by a holistic approach that combines fiber optics, light shaping, and advanced computational algorithms. The recent progress opens up new avenues for minimally invasive deep brain studies in freely behaving mice.

摘要

成像工具的进步一直是神经科学新发现的关键驱动力。能够在自由活动动物的大脑深处可视化神经元和亚细胞结构,对于我们理解神经活动与高级认知功能之间的关系至关重要。然而,快速高分辨率成像仅限于大脑表面以下区域,并且通常需要在显微镜下固定动物头部。开发新方法来应对这些挑战至关重要。在过去几十年中,基于裸光纤的微创内窥技术取得了快速进展。一根单模光纤可用于深入大脑而不会对上覆结构造成重大损伤,并提供高分辨率成像。在这里,我们讨论如何通过结合光纤、光整形和先进计算算法的整体方法来实现高速超分辨率光纤内窥镜检查的全部潜力。最近的进展为在自由活动小鼠中进行微创深部脑研究开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48e3/10917391/327d4b2e2ac9/NPh-011-S11509-g001.jpg

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