In vivo Manganese-enhanced MRI for Visuotopic Brain Mapping

被引:0
|
作者
Chan, Kevin C. [1 ]
Wu, Ed X. [1 ]
机构
[1] Univ Hong Kong, Lab Biomed Imaging & Signal Proc, Hong Kong, Hong Kong, Peoples R China
来源
2012 ANNUAL INTERNATIONAL CONFERENCE OF THE IEEE ENGINEERING IN MEDICINE AND BIOLOGY SOCIETY (EMBC) | 2012年
关键词
MOUSE VISUAL-CORTEX; OCULAR DOMINANCE PLASTICITY; RETINAL GANGLION-CELLS; SUPERIOR COLLICULUS; CHRONIC GLAUCOMA; RAT MODEL; CORTICAL AREAS; OPTIC-NERVE; CONNECTIONS; SYSTEM;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study explored the feasibility of localized manganese-enhanced MRI (MEMRI) via 3 different routes of Mn2+ administrations for visuotopic brain mapping of retinal, callosal, cortico-subcortical, transsynaptic and horizontal connections in normal adult rats. Upon fractionated intravitreal Mn2+ injection, Mn enhancements were observed in the contralateral superior colliculus (SC) and lateral geniculate nucleus (LGN) by 45-60% at 1-3 days after initial Mn2+ injection and in the contralateral primary visual cortex (V1) by about 10% at 2-3 days after initial Mn2+ injection. Direct, single-dose Mn2+ injection to the LGN resulted in Mn enhancement by 13-21% in V1 and 8-11% in SC of the ipsilateral hemisphere at 8 to 24 hours after Mn2+ administration. Intracortical, single-dose Mn2+ injection to the visual cortex resulted in Mn enhancement by 53-65% in ipsilateral LGN, 15-26% in ipsilateral SC, 32-34% in the splenium of corpus callosum and 17-25% in contralateral V1/V2 transition zone at 8 to 24 hours after Mn2+ administration. Notably, some patchy patterns were apparent near the V1/V2 border of the contralateral hemisphere. Laminar-specific horizontal cortical connections were also observed in the ipsilateral hemisphere. The current results demonstrated the sensitivity of MEMRI for assessing the neuroarchitecture of the visual brains in vivo without depth-limitation, and may possess great potentials for studying the basic neural components and connections in the visual system longitudinally during development, plasticity, pharmacological interventions and genetic modifications.
引用
收藏
页码:2279 / 2282
页数:4
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