Larkin Timothy J, Bubb William A, Kuchel Philip W
School of Molecular and Microbial Biosciences, University of Sydney, Australia.
Magn Reson Med. 2008 Apr;59(4):707-11. doi: 10.1002/mrm.21546.
The (1)H magic angle spinning (MAS) NMR spectrum of water in erythrocyte suspensions shows peaks from each of the intracellular and extracellular water pools. The splitting is a true chemical shift and is brought about by the elimination of water exchange under MAS conditions due to physical separation of the two water populations. The size of the chemical shift difference is determined by the concentration of intracellular protein affecting the average extent of hydrogen bonding of water. We present here a model of the chemical shift behavior for water in erythrocytes under normal high-resolution NMR conditions based on results from MAS experiments on these cells exposed to different pH and osmotic conditions. The model accurately predicts the chemical shift of water for a static sample, and the results demonstrate that in high-resolution NMR experiments the chemical shift of water will appear to be invariant if differences in magnetic susceptibility across the cell membrane are minimal (<10% of the magnetic susceptibility of water). Thus, changes in the shape and chemical shift of the water resonance are not due to pH changes in the physiological range. The findings are fundamental to an interpretation of the mechanism of chemical shift effects on the water resonance that may occur in functional MRI.
红细胞悬液中水的氢(¹H)魔角旋转(MAS)核磁共振谱显示了细胞内和细胞外水池中各自的峰。这种分裂是真正的化学位移,是由于在MAS条件下,两种水体因物理分离而消除了水交换所致。化学位移差异的大小由影响水氢键平均程度的细胞内蛋白质浓度决定。基于对这些细胞在不同pH和渗透压条件下进行的MAS实验结果,我们在此提出了正常高分辨率核磁共振条件下红细胞中水的化学位移行为模型。该模型准确预测了静态样品中水的化学位移,结果表明,在高分辨率核磁共振实验中,如果跨细胞膜的磁化率差异最小(<水磁化率的10%),水的化学位移将似乎不变。因此,水共振的形状和化学位移变化并非由于生理范围内的pH变化。这些发现对于解释功能磁共振成像中可能发生的水共振化学位移效应机制至关重要。