Intrinsic optical signal imaging: concurrent assessment of retinal structure and physiological function(报告时间:2012年11月6日上午9:00-11

发布时间:2012-11-05

学术报告


报告题目:
Intrinsic optical signal imaging: concurrent assessment of retinal structure and physiological function
人:Xincheng Yao, Associate Professor of Biomedical Engineering and Vision Sciences, University of Alabama at Birmingham (UAB)
报告时间:11月6日上午9:00-11:00
报告地点:中科院遗传发育所B210报告厅
报告人简介:Xincheng Yao, PhD is an Associate Professor of Biomedical Engineering and Vision Sciences, University of Alabama at Birmingham (UAB). Dr. Yao received his PhD in Optics from the Institute of Physics, Chinese Academy of Sciences in 2001. He worked at Los Alamos National Laboratory as a Postdoctoral Researcher (2001-2004) and Technical Staff Member (2004-2006), and served CFD Research Corporation as a Senior Research Scientist (2006-2007). He joined UAB as an Assistant Professor in 2007, and was appointed as an Associate Professor in 2012. His research interests include biomedical optics instrumentation, functional imaging of the retina, experimental bio-physics of neural systems and pancreatic islets.
讲座摘要:Many eye diseases, such as age-related macular degeneration (AMD), diabetic retinopathy (DR) and glaucoma, involve pathological changes of photo-receptors and/or inner retinal neurons. Given complex structure and delicate function of the retina, both structural and functional measurements are important for retinal diagnosis and treatment evaluation. Since 2004, we have established several imaging approaches, including functional optical coherence tomography (OCT) and confocal microscopy, to investigate transient intrinsic optical signal (IOS) changes in stimulus activated animal (frog and mouse) retinas. High-spatial (μm) and high-temporal (ms) resolution imaging revealed fast IOSs with time courses comparable to retinal electrophysiological kinetics. Fast IOS imaging promises a noninvasive method for concurrent assessment of retinal structure and physiological function. Using mutant mouse retinas and laser-injured frog eyes, we have recently demonstrated the feasibility of IOS mapping of lo-calized retinal dysfunctions.

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