Effects of temperature and aldehyde fixation on tissue water diffusion properties, studied in an erythrocyte ghost tissue model

Ex vivo biological sample imaging can complement in vivo MRI studies. Since ex vivo studies are typically performed at room temperature, and samples are frequently preserved by fixation, it is important to understand how environmental and chemical changes dictated by ex vivo studies alter the physical and MR properties of a sample. Diffusion and relaxation time measurements were used to assess the effects of temperature change and aldehyde fixation on the biophysical and MR properties of a model biological tissue comprised of erythrocyte ghosts suspended in buffer or agarose gel. Sample temperature was varied between 10°C and 37°C. Diffusion MRI data were analyzed with a biophysically appropriate two‐compartment exchange model. Temperature change resulted in a complex alteration of water diffusion properties due to the compartmental nature of tissues and alteration in membrane permeability. Formaldehyde, Karnovsky's solution, and glutaraldehyde all caused statistically significant changes to the biophysical and MR properties of the samples. Fixation caused large decreases in water proton T2, which was restored to near prefixation values by washing free fixative from the samples. Water membrane permeability was also significantly altered by fixation. This study demonstrates that relating in vivo MR data to chemically fixed ex vivo data requires an understanding of the effects of sample preparation. Magn Reson Med, 2006. © 2006 Wiley‐Liss, Inc.

[1]  E. Stejskal Use of Spin Echoes in a Pulsed Magnetic‐Field Gradient to Study Anisotropic, Restricted Diffusion and Flow , 1965 .

[2]  J. E. Tanner,et al.  Spin diffusion measurements : spin echoes in the presence of a time-dependent field gradient , 1965 .

[3]  A. L. V. Geet Calibration of the methanol and glycol nuclear magnetic resonance thermometers with a static thermistor probe , 1968 .

[4]  R. Mills,et al.  Self-diffusion in normal and heavy water in the range 1-45.deg. , 1973 .

[5]  P. G. Wood [27] Preparation of white resealable erythrocyte ghosts , 1987 .

[6]  Preparation of white resealable erythrocyte ghosts. , 1987, Methods in enzymology.

[7]  R E Latchaw,et al.  Anatomy of the brainstem: correlation of in vitro MR images with histologic sections. , 1989, AJNR. American journal of neuroradiology.

[8]  G Benga,et al.  On measuring the diffusional water permeability of human red blood cells and ghosts by nuclear magnetic resonance. , 1990, Journal of biochemical and biophysical methods.

[9]  M. Tovi,et al.  Measurements of T1 and T2 over time in formalin-fixed human whole-brain specimens. , 1992, Acta radiologica.

[10]  R. Ideker,et al.  Magnetic resonance imaging of chronic myocardial infarcts in formalin-fixed human autopsy hearts. , 1994, Circulation.

[11]  B. Dardzinski,et al.  Temperature Dependent Change of Apparent Diffusion Coefficient of Water in Normal and Ischemic Brain of Rats , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[12]  A. Leroy-Willig,et al.  Simultaneous measurements of diffusion and transverse relaxation in exercising skeletal muscle. , 1995, Magnetic resonance imaging.

[13]  G. Maurer,et al.  NMR Spectroscopic and Densimetric Study of Reaction Kinetics of Formaldehyde Polymer Formation in Water, Deuterium Oxide, and Methanol , 1995 .

[14]  R M Henkelman,et al.  Integrated analysis of diffusion and relaxation of water in blood , 1998, Magnetic resonance in medicine.

[15]  E Falk,et al.  Effects of temperature and histopathologic preparation on the size and morphology of atherosclerotic carotid arteries as imaged by MRI , 1999, Journal of magnetic resonance imaging : JMRI.

[16]  R L Winslow,et al.  Direct histological validation of diffusion tensor MRI in formaldehyde‐fixed myocardium , 2000, Magnetic resonance in medicine.

[17]  T. Zeuthen How water molecules pass through aquaporins. , 2001, Trends in biochemical sciences.

[18]  L. Hedlund,et al.  Morphologic phenotyping with MR microscopy: the visible mouse. , 2002, Radiology.

[19]  S. Blackband,et al.  MR microscopy and high resolution small animal MRI: applications in neuroscience research , 2002, Progress in Neurobiology.

[20]  S. Blackband,et al.  Ex vivo High-Resolution Magnetic Resonance Imaging of the Brain in Joubert's Syndrome , 2002, Journal of child neurology.

[21]  Stephen J Blackband,et al.  Human erythrocyte ghosts: Exploring the origins of multiexponential water diffusion in a model biological tissue with magnetic resonance , 2002, Magnetic resonance in medicine.

[22]  T. Mareci,et al.  Anatomical Studies in the Rodent Brain and Spinal Cord: Applications of Magnetic Resonance Microscopy , 2002 .

[23]  L. Hedlund,et al.  Magnetic resonance histology for morphologic phenotyping , 2002, Journal of magnetic resonance imaging : JMRI.

[24]  P. Hof,et al.  Cytoarchitecture of the human cerebral cortex: MR microscopy of excised specimens at 9.4 Tesla. , 2002, AJNR. American journal of neuroradiology.

[25]  Sheng-Kwei Song,et al.  Relative indices of water diffusion anisotropy are equivalent in live and formalin‐fixed mouse brains , 2003, Magnetic resonance in medicine.

[26]  Hao Huang,et al.  Three-dimensional anatomical characterization of the developing mouse brain by diffusion tensor microimaging , 2003, NeuroImage.

[27]  Edith V. Sullivan,et al.  Postmortem MR imaging of formalin-fixed human brain , 2004, NeuroImage.

[28]  Hsiao-Fang Liang,et al.  Formalin fixation alters water diffusion coefficient magnitude but not anisotropy in infarcted brain , 2005, Magnetic resonance in medicine.

[29]  Susumu Mori,et al.  Magnetic Resonance Diffusion Tensor Microimaging Reveals a Role for Bcl-x in Brain Development and Homeostasis , 2005, The Journal of Neuroscience.