Quantitative activity-induced manganese-dependent MRI for characterizing cortical layers in the primary somatosensory cortex of the rat

被引:2
作者
Auffret, Matthieu [1 ]
Samim, Idrees [1 ]
Lepore, Mario [1 ]
Gruetter, Rolf [1 ]
Just, Nathalie [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Ctr Imagerie Biomed Anim Imaging & Technol Core C, Lab Funct & Metab Imaging LIFMET, CH-1015 Lausanne, Switzerland
关键词
Manganese; Histograms; Barrel cortex; Thalamus; Cortical layers; RESONANCE-IMAGING MEMRI; BARREL CORTEX; ENHANCED MRI; WHISKER STIMULATION; PYRAMIDAL NEURONS; DENDRITIC CALCIUM; BOLD FMRI; ACTIVATION; RESPONSES;
D O I
10.1007/s00429-014-0933-3
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The ability of Mn2+ to follow Ca2+ pathways upon stimulation transform them into remarkable surrogate markers of neuronal activity using activity-induced manganese-dependent MRI (AIM-MRI). In the present study, a precise follow-up of physiological parameters during MnCl2 and mannitol infusions improved the reproducibility of AIM-MRI allowing in-depth evaluation of the technique. Pixel-by-pixel T-1 data were investigated using histogram distributions in the barrel cortex (BC) and the thalamus before and after Mn2+ infusion, after blood brain barrier opening and after BC activation. Mean BC T-1 values dropped significantly upon trigeminal nerve (TGN) stimulation (-38 %, P = 0.02) in accordance with previous literature findings. T-1 histogram distributions showed that 34 % of T-1s in the range 600-1500 ms after Mn2+ + mannitol infusions shifted to 50-350 ms after TGN stimulation corresponding to a twofold increase of the percentage of pixels with the lowest T-1s in BC. Moreover, T-1 changes in response to stimulation increased significantly from superficial cortical layers (I-III) to deeper layers (V-VI). Cortical cytoarchitecture detection during a functional paradigm was performed extending the potential of AIM-MRI. Quantitative AIM-MRI could thus offer a means to interpret local neural activity across cortical layers while identification of the role of calcium dynamics in vivo during brain activation could play a key role in resolving neurovascular coupling mechanisms.
引用
收藏
页码:695 / 707
页数:13
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