An in vivo implementation of the MEX MRI for myelin fraction of mice brain.


Journal

Magma (New York, N.Y.)
ISSN: 1352-8661
Titre abrégé: MAGMA
Pays: Germany
ID NLM: 9310752

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 28 04 2021
accepted: 26 07 2021
revised: 11 07 2021
pubmed: 7 8 2021
medline: 13 4 2022
entrez: 6 8 2021
Statut: ppublish

Résumé

Magnetization EXchange (MEX) sequence measures a signal linearly dependent on the myelin proton fraction by selective suppression of water magnetization and a recovery period. Varying the recovery period enables extraction of the percentile fraction of myelin bound protons. We aim to demonstrate the MEX sequence sensitivity to the fraction of protons associated with myelin in mice brain, in vivo. The cuprizone mouse model was used to manipulate the myelin content. Mice fed cuprizone (n = 15) and normal chow (n = 8) were imaged in vivo using MEX sequence. MR images were segmented into corpus callosum and internal capsule (white matter) and cortical gray matter, and fitted to the recovery equation. Results were analyzed with correlation to MWF and histopathology. The extracted parameters show significant differences in the corpus callosum between the cuprizone and control groups. The cuprizone group exhibited reduced myelin fraction 26.5% (P < 0.01). The gray matter values were less affected, with 13.5% reduction (P < 0.05); no changes were detected in the internal capsule. Results were validated by MWF scans and good correlation to the histology analysis (R The results of this first in vivo implementation of the MEX sequence provide a quantitative measure of demyelination in brain white matter.

Identifiants

pubmed: 34357453
doi: 10.1007/s10334-021-00950-z
pii: 10.1007/s10334-021-00950-z
doi:

Substances chimiques

Protons 0
Cuprizone 5N16U7E0AO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

267-276

Subventions

Organisme : Israel Science Foundation
ID : 1585/17
Organisme : United States - Israel Binational Science Foundation
ID : 2013253

Informations de copyright

© 2021. European Society for Magnetic Resonance in Medicine and Biology (ESMRMB).

Références

Mehta RC, Pike GB, Enzmann DR (1996) Magnetization transfer magnetic resonance imaging: a clinical review. Top Magn Reson Imaging 8(4):214–230
doi: 10.1097/00002142-199608000-00002
van Zijl PCM, Lam WW, Xu J, Knutsson L, Stanisz GJ (2018) Magnetization transfer contrast and chemical exchange saturation transfer MRI. Features and analysis of the field-dependent saturation spectrum. Neuroimage 168:222–241. https://doi.org/10.1016/j.neuroimage.2017.04.045
doi: 10.1016/j.neuroimage.2017.04.045 pubmed: 28435103
McKeithan LJ, Lyttle BD, Box BA et al (2019) 7T quantitative magnetization transfer (qMT) of cortical gray matter in multiple sclerosis correlates with cognitive impairment. Neuroimage 203:116190. https://doi.org/10.1016/j.neuroimage.2019.116190
doi: 10.1016/j.neuroimage.2019.116190 pubmed: 31525497
Dortch RD, Li K, Gochberg DF et al (2011) Quantitative magnetization transfer imaging in human brain at 3 T via selective inversion recovery. Magn Reson Med 66(5):1346–1352. https://doi.org/10.1002/mrm.22928
doi: 10.1002/mrm.22928 pubmed: 21608030 pmcid: 3285505
Gochberg DF, Kennan RP, Gore JC (1997) Quantitative studies of magnetization transfer by selective excitation and T1 recovery. Magn Reson Med 38(2):224–231. https://doi.org/10.1002/mrm.1910380210
doi: 10.1002/mrm.1910380210 pubmed: 9256101
Dortch RD, Bagnato F, Gochberg DF, Gore JC, Smith SA (2018) Optimization of selective inversion recovery magnetization transfer imaging for macromolecular content mapping in the human brain. Magn Reson Med 80(5):1824–1835. https://doi.org/10.1002/mrm.27174
doi: 10.1002/mrm.27174 pubmed: 29573356 pmcid: 6107392
Wilhelm MJ, Ong HH, Wehrli SL et al (2012) Direct magnetic resonance detection of myelin and prospects for quantitative imaging of myelin density. Proc Natl Acad Sci USA 109(24):9605–9610. https://doi.org/10.1073/pnas.1115107109
doi: 10.1073/pnas.1115107109 pubmed: 22628562 pmcid: 3386098
Du J, Ma G, Li S et al (2014) Ultrashort echo time (UTE) magnetic resonance imaging of the short T2 components in white matter of the brain using a clinical 3T scanner. Neuroimage 87:32–41. https://doi.org/10.1016/j.neuroimage.2013.10.053
doi: 10.1016/j.neuroimage.2013.10.053 pubmed: 24188809
Campbell JSW, Leppert IR, Narayanan S et al (2018) Promise and pitfalls of g-ratio estimation with MRI. Neuroimage 182:80–96. https://doi.org/10.1016/j.neuroimage.2017.08.038
doi: 10.1016/j.neuroimage.2017.08.038 pubmed: 28822750
Stikov N, Campbell JSW, Stroh T et al (2015) In vivo histology of the myelin g-ratio with magnetic resonance imaging. Neuroimage 118:397–405. https://doi.org/10.1016/j.neuroimage.2015.05.023
doi: 10.1016/j.neuroimage.2015.05.023 pubmed: 26004502
Laule C, Vavasour IM, Kolind SH et al (2007) Magnetic resonance imaging of myelin. Neurotherapeutics 4(3):460–484. https://doi.org/10.1016/j.nurt.2007.05.004
doi: 10.1016/j.nurt.2007.05.004 pubmed: 17599712 pmcid: 7479725
Laule C, Moore GRW (2018) Myelin water imaging to detect demyelination and remyelination and its validation in pathology. Brain Pathol 28(5):750–764. https://doi.org/10.1111/bpa.12645
doi: 10.1111/bpa.12645 pubmed: 30375119 pmcid: 8028667
Alonso-Ortiz E, Levesque IR, Pike GB (2015) MRI-based myelin water imaging: a technical review. Magn Reson Med 73(1):70–81. https://doi.org/10.1002/mrm.25198
doi: 10.1002/mrm.25198 pubmed: 24604728
Leandrou S, Petroudi S, Kyriacou PA, Reyes-Aldasoro CC, Pattichis CS (2018) Quantitative MRI Brain studies in mild cognitive impairment and Alzheimer’s disease: a methodological review. IEEE Rev Biomed Eng 11:97–111. https://doi.org/10.1109/RBME.2018.2796598
doi: 10.1109/RBME.2018.2796598 pubmed: 29994606
Ben-Eliezer N, Sodickson DK, Block KT (2015) Rapid and accurate T2 mapping from multi-spin-echo data using Bloch-simulation-based reconstruction. Magn Reson Med 73(2):809–817. https://doi.org/10.1002/mrm.25156
doi: 10.1002/mrm.25156 pubmed: 24648387
Eliav U, Navon G (2017) The role of magnetization transfer in the observed contrast in T1weighted imaging under clinical setups. NMR Biomed 30(12):e3792. https://doi.org/10.1002/nbm.3792
doi: 10.1002/nbm.3792
Edzes HT, Samulski ET (1978) The measurement of cross-relaxation effects in the proton NMR spin-lattice relaxation of water in biological systems: hydrated collagen and muscle. J Magn Reson 31(2):207–229. https://doi.org/10.1016/0022-2364(78)90185-3
doi: 10.1016/0022-2364(78)90185-3
Morrison C, Mark HR (1995) A model for magnetization transfer in tissues. Magn Reson Med 33(4):475–482. https://doi.org/10.1002/mrm.1910330404
doi: 10.1002/mrm.1910330404 pubmed: 7776877
Callaghan PT (1991) Principles of nuclear magnetic resonance microscopy. Med Phys. https://doi.org/10.1118/1.596918
doi: 10.1118/1.596918
Bydder GM, Hajnal JV, Young IR (1998) MRI: Use of the inversion recovery pulse sequence. Clin Radiol 53(3):159–176. https://doi.org/10.1016/S0009-9260(98)80096-2
doi: 10.1016/S0009-9260(98)80096-2 pubmed: 9528866
Gochberg DF, Gore JC (2007) Quantitative magnetization transfer imaging via selective inversion recovery with short repetition times. Magn Reson Med 57(2):437–441. https://doi.org/10.1002/mrm.21143
doi: 10.1002/mrm.21143 pubmed: 17260381 pmcid: 2634834
Torkildsen A, Brunborg LA, Myhr KM, Bø L (2008) The cuprizone model for demyelination. Acta Neurol Scand 117(SUPPL 188):72–76. https://doi.org/10.1111/j.1600-0404.2008.01036.x
doi: 10.1111/j.1600-0404.2008.01036.x
Matsushima GK, Morell P (2006) The neurotoxicant, cuprizone, as a model to study demyelination and remyelination in the central nervous system. Brain Pathol 11(1):107–116. https://doi.org/10.1111/j.1750-3639.2001.tb00385.x
doi: 10.1111/j.1750-3639.2001.tb00385.x pmcid: 8098267
Teklad Custom Diets (2016) Research models and services teklad custom diets cuprizone diets: a trusted tool for neuroscience research https://www.mendeley.com/catalogue/f2ef99c6-
Ding S, Guo Y, Chen X et al (2021) Demyelination and remyelination detected in an alternative cuprizone mouse model of multiple sclerosis with 7.0 T multiparameter magnetic resonance imaging. Sci Rep 11(1):1–11. https://doi.org/10.1038/s41598-021-90597-6
doi: 10.1038/s41598-021-90597-6
Mullin AP, Cui C, Wang Y et al (2017) rHIgM22 enhances remyelination in the brain of the cuprizone mouse model of demyelination. Neurobiol Dis 105:142–155. https://doi.org/10.1016/J.NBD.2017.05.015
doi: 10.1016/J.NBD.2017.05.015 pubmed: 28576706
Steelman AJ, Thompson JP, Li J (2012) Demyelination and remyelination in anatomically distinct regions of the corpus callosum following cuprizone intoxication. Neurosci Res 72(1):32–42. https://doi.org/10.1016/J.NEURES.2011.10.002
doi: 10.1016/J.NEURES.2011.10.002 pubmed: 22015947
Wang Z, Baharani A, Wei Z et al (2021) Low field magnetic stimulation promotes myelin repair and cognitive recovery in chronic cuprizone mouse model. Clin Exp Pharmacol Physiol 48(8):1090–1102. https://doi.org/10.1111/1440-1681.13490
doi: 10.1111/1440-1681.13490 pubmed: 33638234
Saskia Hübner N, Mechling AE, Lee HL et al (2017) The connectomics of brain demyelination: Functional and structural patterns in the cuprizone mouse model. Neuroimage 146:1–18. https://doi.org/10.1016/J.NEUROIMAGE.2016.11.008
doi: 10.1016/J.NEUROIMAGE.2016.11.008
Eliav U, Ronen I, Halock K, Kim DSNGM (2007) Magnetization exchange (MEX) MRI: a clinically viable protein-based imaging method. ISMRM-ESMRMB meeting. Springer, Berlin
Stanisz GJ, Kecojevic A, Bronskill MJ, Henkelman RM (1999) Characterizing white matter with magnetization transfer and T2. Magn Reson Med 42(6):1128–1136. https://doi.org/10.1002/(SICI)1522-2594(199912)42:6%3c1128::AID-MRM18%3e3.0.CO;2-9
doi: 10.1002/(SICI)1522-2594(199912)42:6<1128::AID-MRM18>3.0.CO;2-9 pubmed: 10571935
Leibfritz D, Dreher W (2001) Magnetization transfer MRS. NMR Biomed 14(2):65–76. https://doi.org/10.1002/nbm.681
doi: 10.1002/nbm.681 pubmed: 11320534
Smith SA, Edden RAE, Farrell JAD, Barker PB, Van Zijl PCM (2008) Measurement of T
doi: 10.1002/mrm.21596 pubmed: 18581383 pmcid: 2887301
van Gelderen P, Jiang X, Duyn JH (2016) Effects of magnetization transfer on T1 contrast in human brain white matter. Neuroimage 128:85–95. https://doi.org/10.1016/j.neuroimage.2015.12.032
doi: 10.1016/j.neuroimage.2015.12.032 pubmed: 26724780
Fatouros PP, Marmarou A (1999) Use of magnetic resonance imaging for in vivo measurements of water content in human brain: method and normal values. J Neurosurg 90(1):109–115. https://doi.org/10.3171/jns.1999.90.1.0109
doi: 10.3171/jns.1999.90.1.0109 pubmed: 10413163
Edzes H, Nature ES (1977) Cross relaxation and spin diffusion in the proton NMR of hydrated collagen. Springer, Berlin. https://doi.org/10.1038/265521a0
doi: 10.1038/265521a0
Eliav U, Navon G (2002) Multiple quantum filtered NMR studies of the interaction between collagen and water in the tendon. J Am Chem Soc 124(12):3125–3132
doi: 10.1021/ja011791n
Dula AN, Gochberg DF, Valentine HL, Valentine WM, Does MD (2010) Multiexponential T2, magnetization transfer, and quantitative histology in white matter tracts of rat spinal cord. Magn Reson Med 63(4):902–909. https://doi.org/10.1002/mrm.22267
doi: 10.1002/mrm.22267 pubmed: 20373391 pmcid: 2852261
Hiremath MM, Saito Y, Knapp GW, Ting JP-Y, Suzuki K, Matsushima GK (1998) Microglial/macrophage accumulation during cuprizone-induced demyelination in C57BL/6 mice. J Neuroimmunol 92(1–2):38–49. https://doi.org/10.1016/S0165-5728(98)00168-4
doi: 10.1016/S0165-5728(98)00168-4 pubmed: 9916878
Dorr AE, Lerch JP, Spring S, Kabani N, Henkelman RM (2008) High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice. Neuroimage 42(1):60–69. https://doi.org/10.1016/j.neuroimage.2008.03.037
doi: 10.1016/j.neuroimage.2008.03.037 pubmed: 18502665
Bjarnason TA, Mitchell JR (2010) AnalyzeNNLS: magnetic resonance multiexponential decay image analysis. J Magn Reson 206(2):200–204. https://doi.org/10.1016/j.jmr.2010.07.008
doi: 10.1016/j.jmr.2010.07.008 pubmed: 20688549
Hibbits N, Yoshino J, Le TQ, Armstrong RC (2012) Astrogliosis during acute and chronic cuprizone demyelination and implications for remyelination. ASN Neuro 4(6):AN20120062. https://doi.org/10.1042/AN20120062
doi: 10.1042/AN20120062
Turati L, Moscatelli M, Mastropietro A et al (2015) In vivo quantitative magnetization transfer imaging correlates with histology during de- and remyelination in cuprizone-treated mice. NMR Biomed 28(3):327–337. https://doi.org/10.1002/nbm.3253
doi: 10.1002/nbm.3253 pubmed: 25639498

Auteurs

Ella Wilczynski (E)

Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv, Israel.

Efrat Sasson (E)

School of Chemistry, Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, Israel.

Uzi Eliav (U)

School of Chemistry, Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, Israel.

Gil Navon (G)

School of Chemistry, Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, Israel.

Uri Nevo (U)

Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv, Israel. nevouri@tauex.tau.ac.il.
Sagol School of Neuroscience, Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel. nevouri@tauex.tau.ac.il.

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