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Abstract #2274

Diffusion fMRI of mouse optic nerve with antidromic electrical stimulation

Tsen-Hsuan (Abby) Lin1, Willaim M Spees1,2, Michael Wallendorf3, Yen-Yu Ian Shih4, Anne H Cross2,5, and Sheng-Kwei Song1,2,6

1Radiology, Washington University School of Medicine, St. Louis, MO, United States, 2The Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO, United States, 3Biostatistics, Washington University School of Medicine, St. Louis, MO, United States, 4Neurology, The University of North Carolina in Chapel Hill, NC, United States, 5Neurology, Washington University School of Medicine, St. Louis, MO, United States, 6Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, United States

Previously, we have successfully employed diffusion fMRI (dfMRI) to assess impaired axonal function in experimental autoimmune encephalomyelitis (EAE) mice undergoing visual stimulation. However, the prior dfMRI experiments cannot resolve contributions from retinal dysfunction to the decreased dfMRI changes observed in EAE mice. To address this shortcoming, we implanted an MR-compatible tungsten electrode at lateral geniculate nucleus (LGN) to perform antidromic stimulation of optic nerves. We demonstrated perpendicular apparent diffusion coefficient decreased with antidromic electrical stimulation at LGN bypassing visual input through retina.

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