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(17)16.4特斯拉下大鼠大脑中的O弛豫时间。

(17)O relaxation times in the rat brain at 16.4 tesla.

作者信息

Wiesner Hannes M, Balla Dávid Z, Shajan G, Scheffler Klaus, Uğurbil Kâmil, Chen Wei, Uludağ Kâmil, Pohmann Rolf

机构信息

High-Field Magnetic Resonance Center, Max Planck Institute for Biological Cybernetics, Tübingen, Germany.

Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota Medical School, Minneapolis, Minnesota, USA.

出版信息

Magn Reson Med. 2016 May;75(5):1886-93. doi: 10.1002/mrm.25814. Epub 2015 Jun 22.

Abstract

PURPOSE

Measurement of the cerebral metabolic rate of oxygen (CMRO2 ) by means of direct imaging of the (17) O signal can be a valuable tool in neuroscientific research. However, knowledge of the longitudinal and transverse relaxation times of different brain tissue types is required, which is difficult to obtain because of the low sensitivity of natural abundance H2 (17) O measurements.

METHODS

Using the improved sensitivity at a field strength of 16.4 Tesla, relaxation time measurements in the rat brain were performed in vivo and postmortem with relatively high spatial resolutions, using a chemical shift imaging sequence.

RESULTS

In vivo relaxation times of rat brain were found to be T1 = 6.84 ± 0.67 ms and T2 * = 1.77 ± 0.04 ms. Postmortem H2 (17) O relaxometry at enriched concentrations after inhalation of (17) O2 showed similar T2 * values for gray matter (1.87 ± 0.04 ms) and white matter, significantly longer than muscle (1.27 ± 0.05 ms) and shorter than cerebrospinal fluid (2.30 ± 0.16 ms).

CONCLUSION

Relaxation times of brain H2 (17) O were measured for the first time in vivo in different types of tissues with high spatial resolution. Because the relaxation times of H2 (17) O are expected to be independent of field strength, our results should help in optimizing the acquisition parameters for experiments also at other MRI field strengths.

摘要

目的

通过对¹⁷O信号进行直接成像来测量脑氧代谢率(CMRO₂),这在神经科学研究中可能是一种有价值的工具。然而,需要了解不同脑组织类型的纵向和横向弛豫时间,由于天然丰度H₂¹⁷O测量的低灵敏度,这很难获得。

方法

利用在16.4特斯拉场强下提高的灵敏度,使用化学位移成像序列,在大鼠脑内和死后以相对高的空间分辨率进行弛豫时间测量。

结果

发现大鼠脑内的弛豫时间为T1 = 6.84 ± 0.67毫秒,T2* = 1.77 ± 0.04毫秒。吸入¹⁷O₂后在富集浓度下进行的死后H₂¹⁷O弛豫测量显示,灰质(1.87 ± 0.04毫秒)和白质的T2*值相似,明显长于肌肉(1.27 ± 0.05毫秒)且短于脑脊液(2.30 ± 0.16毫秒)。

结论

首次在体内以高空间分辨率测量了不同类型脑组织中脑H₂¹⁷O的弛豫时间。由于预计H₂¹⁷O的弛豫时间与场强无关,我们的结果应有助于优化在其他MRI场强下实验的采集参数。

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