The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
MR imaging of the amide‐proton transfer effect and the pH‐insensitive nuclear overhauser effect at 9.4 T
Open accessAbstract
The amide proton transfer (APT) effect has emerged as a unique endogenous molecular imaging contrast mechanism with great clinical potentials. However, in vivo quantitative mapping of APT using the conventional asymmetry analysis is difficult due to the confounding nuclear Overhauser effect (NOE) and the asymmetry of the magnetization transfer effect. Here, we showed that the asymmetry of magnetization transfer contrast from immobile macromolecules is highly significant, and the wide spectral separation associated with a high magnetic field of 9.4 T delineates APT and NOE peaks in a Z‐spectrum. Therefore, high‐resolution apparent APT and NOE maps can be obtained from measurements at three offsets. The apparent APT value was greater in gray matter compared to white matter in normal rat brain and was sensitive to tissue acidosis and correlated well with apparent diffusion coefficient in the rat focal ischemic brain. In contrast, no ischemia‐induced contrast was observed in the apparent NOE map. The concentration dependence and the pH insensitivity of NOE were confirmed in phantom experiments. Our results demonstrate that in vivo apparent APT and NOE maps can be easily obtained at high magnetic fields and the pH‐insensitive NOE may be a useful indicator of mobile macromolecular contents. Magn Reson Med, 2013. © 2012 Wiley Periodicals, Inc.
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Cites
Kumar, A., Ernst, R. R., & Wüthrich, K. (1980) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(80)90695-6 · Cited by 1,905
Bothner-By, A. A., Stephens, R. L., Lee, J., Warren, C. D., & Jeanloz, R. W. (1984) · Journal of the American Chemical Society · doi:10.1021/ja00315a069 · Cited by 1,654
Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo
Wolff, S. D., & Balaban, R. S. (1989) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910100113 · Cited by 1,482
Ward, K. M., Aletras, A. H., & Balaban, R. S. (2000) · Journal of Magnetic Resonance · doi:10.1006/jmre.1999.1956 · Cited by 1,429
Using the amide proton signals of intracellular proteins and peptides to detect pH effects in MRI
Zhou, J., Payen, J.-F., Wilson, D. A., Traystman, R. J., & van Zijl, P. C. M. (2003) · Nature Medicine · doi:10.1038/nm907 · Cited by 1,198
Chemical exchange saturation transfer (CEST): what is in a name and what isn't?
van Zijl, P. C. M., & Yadav, N. N. (2011) · Magnetic Resonance in Medicine · doi:10.1002/mrm.22761 · Cited by 1,155
Experimental studies of ischemic brain edema
Koizumi, J.-I., Yoshida, Y., Nakazawa, T., & Ooneda, G. (1986) · Nosotchu · doi:10.3995/jstroke.8.1 · Cited by 996
Magnetization transfer in MRI: a review
Henkelman, R. M., Stanisz, G. J., & Graham, S. J. (2001) · NMR in Biomedicine · doi:10.1002/nbm.683 · Cited by 921
Koizumi, J. (1986) · Medical Entomology and Zoology · Cited by 762
Kim, M., Gillen, J., Landman, B. A., Zhou, J., & van Zijl, P. C. M. (2009) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21873 · Cited by 691
Dousset, V, Grossman, R. I., Ramer, K. N., Schnall, M. D., Young, L. H., Gonzalez-Scarano, F., Lavi, E., & Cohen, J. A. (1992) · Radiology · doi:10.1148/radiology.182.2.1732968 · Cited by 690
Ling, W., Regatte, R. R., Navon, G., & Jerschow, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707666105 · Cited by 533
Zhou, J., Tryggestad, E., Wen, Z., Lal, B., Zhou, T., Grossman, R., Wang, S., Yan, K., Fu, D.-X., Ford, E., et al. (2011) · Nature Medicine · doi:10.1038/nm.2268 · Cited by 526
Practical data acquisition method for human brain tumor amide proton transfer (APT) imaging
Zhou, J., Blakeley, J. O., Hua, J., Kim, M., Laterra, J., Pomper, M. G., & van Zijl, P. C. M. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21712 · Cited by 338
Detection of the Ischemic Penumbra Using pH-Weighted MRI
Sun, P. Z., Zhou, J., Sun, W., Huang, J., & van Zijl, P. C. (2007) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600424 · Cited by 334
A Model for Magnetization Transfer in Tissues
Morrison, C., & Mark Henkelman, R. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910330404 · Cited by 305
van Zijl, P. C. M., Zhou, J., Mori, N., Payen, J., Wilson, D., & Mori, S. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10398 · Cited by 230
Hua, J., Jones, C. K., Blakeley, J., Smith, S. A., van Zijl, P. C. M., & Zhou, J. (2007) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21387 · Cited by 222
Jones, C. K., Polders, D., Hua, J., Zhu, H., Hoogduin, H. J., Zhou, J., Luijten, P., & van Zijl, P. C. M. (2012) · Magnetic Resonance in Medicine · doi:10.1002/mrm.23141 · Cited by 209
Characterization of macromolecule resonances in the 1H NMR spectrum of rat brain
Behar, K. L., & Ogino, T. (1993) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910300107 · Cited by 204
Morrison, C., Stanisz, G., & Henkelman, R. M. (1995) · Journal of Magnetic Resonance, Series B · doi:10.1006/jmrb.1995.1111 · Cited by 174
Magnetic resonance imaging of the Amine–Proton EXchange (APEX) dependent contrast
Jin, T., Wang, P., Zong, X., & Kim, S.-G. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.014 · Cited by 169
Self-citationProton transfer ratio, lactate, and intracellular pH in acute cerebral ischemia
Jokivarsi, K. T., Gröhn, H. I., Gröhn, O. H. J., & Kauppinen, R. A. (2007) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21181 · Cited by 138
Simplified quantitative description of amide proton transfer (APT) imaging during acute ischemia
Sun, P. Z., Zhou, J., Huang, J., & van Zijl, P. C. M. (2007) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21151 · Cited by 136
Li, A. X., Hudson, R. H. E., Barrett, J. W., Jones, C. K., Pasternak, S., & Bartha, R. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21752 · Cited by 112
Proton NMR spectroscopy of solvent‐saturable resonances: A new approach to study pH effects in Situ
Mori, S., Eleff, S. M., Pilatus, U., Mori, N., & van Zijl, P. C. M. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910400105 · Cited by 111
Scheidegger, R., Vinogradov, E., & Alsop, D. C. (2011) · Magnetic Resonance in Medicine · doi:10.1002/mrm.22912 · Cited by 102
Kuo, Y., Herlihy, A. H., So, P., Bhakoo, K. K., & Bell, J. D. (2005) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.20285 · Cited by 99
Magnetization transfer phenomenon in the human brain at 7 T
Mougin, O. E., Coxon, R., Pitiot, A., & Gowland, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.08.022 · Cited by 98
Early Experience of Translating pH-Weighted MRI to Image Human Subjects at 3 Tesla
Sun, P. Z., Benner, T., Copen, W. A., & Sorensen, A. G. (2010) · Stroke · doi:10.1161/strokeaha.110.595777 · Cited by 82
Change of the cerebrospinal fluid volume during brain activation investigated by T1ρ-weighted fMRI
Jin, T., & Kim, S. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.047 · Cited by 61
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van Zijl, P. C. M., Lam, W. W., Xu, J., Knutsson, L., & Stanisz, G. J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.04.045 · Cited by 339
Zaiss, M., & Bachert, P. (2013) · Physics in Medicine and Biology · doi:10.1088/0031-9155/58/22/r221 · Cited by 323
Noninvasive Detection of Extracellular pH in Human Benign and Malignant Liver Tumors Using CEST MRI
Tang, Y., Xiao, G., Shen, Z., Zhuang, C., Xie, Y., Zhang, X., Yang, Z., Guan, J., Shen, Y., Chen, Y., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.578985 · Cited by 56
Xiao, P., Huang, J., Han, X., Cheu, J. W. S., Liu, Y., Law, L. H., Lai, J. H. C., Li, J., Park, S. W., Wong, C. C. L., et al. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c10493 · Cited by 14
Metadata
- Authors
- Jin, T., Wang, P., Zong, X., & Kim, S.
- Venue
- Magnetic Resonance in Medicine
- Publisher
- Wiley
- Published
- 2012-05-10
- Volume
- 69
- Issue
- 3
- Pages
- 760-770
- ISSN
- 0740-3194 (ISSN-L)
- 1522-2594
- OpenAlex
- W1969935384
- Cited by
- 273
- References
- 31
- FWCI
- 11.13
- Type
- journal article
- Language
- en
- Open access
- bronze
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