Modern neuroimaging such as fMRI and PET has opened up enormously exciting frontiers for studying brain function and human behavior. Understanding the relation between the imaging signals and the underlying brain physiology has become increasingly important and urgent. Although tremendous insights about neurovascular coupling have been gained, it is still elusive of the quantitative relation between brain metabolic energy and neuronal activity (i.e., neurometabolic coupling). Particularly important and intensely debated question is how much increases of cerebral metabolic rate of oxygen (CMRO2) are needed, or can be provided by brain for supporting task-evoked neuronal activity. The major challenge in this regard is the lack of a fast, noninvasive and quantitative method able to directly image absolute CMRO2 at both basal and activated brain states. The high-field 17O MRS imaging (MRSI) approach for imaging CMRO2 which has been successfully developed by us over the first funding cycle could overcome this hurdle. This innovative and unique approach offers a golden opportunity for studying the neurometabolic coupling and its impact on brain function. A large body of our preliminary results has not only demonstrated the feasibility, reliability and applicability of this 17O-based CMRO2 imaging approach, but also provided crucial evidence showing the importance and possible mechanism of cerebral oxidative metabolism for supporting brain energy at rest and during activation. These findings lead us to hypothesize that cerebral oxidative metabolism should be the major energy source for both resting and activated brain due to the tight neurometabolic coupling;however, its capacity might be limited which in large is used for intrinsic brain activity at rest;thus, there exist a strong correlation between task-evoked CMRO2 change and baseline CMRO2, and an energy compensation mechanism for utilizing brain energy during brain activation with optimal efficacy. This central hypothesis will be examined in the cat brain through four testable hypotheses and four specific aims by using 17O-based CMRO2 imaging approach combined with other established approaches including electrophysiology recording. This research will (i) highlight the importance of cerebral oxidative metabolism at both baseline and activated brain states;(ii) elucidate the mechanism of cerebral bioenergetics associated with neuronal activity and brain function;and (iii) provide the neurophysiology basis for modern neuroimaging techniques. Relevance to public health: This research could provide new insights about crucial impact of cerebral oxidative metabolism on the brain disorders and dysfunctions associated with oxidative metabolism abnormality. The success in developing the 17O-based CMRO2 imaging modality will further enhance the ability of MR technology in neuroscience discovery and potentially in diagnosis of brain diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS041262-09
Application #
7874450
Study Section
Medical Imaging Study Section (MEDI)
Program Officer
Jacobs, Tom P
Project Start
2001-04-01
Project End
2012-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
9
Fiscal Year
2010
Total Cost
$465,320
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Zhu, Xiao-Hong; Chen, Wei (2018) In vivo X-Nuclear MRS Imaging Methods for Quantitative Assessment of Neuroenergetic Biomarkers in Studying Brain Function and Aging. Front Aging Neurosci 10:394
Zhu, Xiao-Hong; Chen, Wei (2017) In vivo17O MRS imaging - Quantitative assessment of regional oxygen consumption and perfusion rates in living brain. Anal Biochem 529:171-178
Einstein, Samuel A; Weegman, Bradley P; Kitzmann, Jennifer P et al. (2017) Noninvasive assessment of tissue-engineered graft viability by oxygen-17 magnetic resonance spectroscopy. Biotechnol Bioeng 114:1118-1121
Wiesner, Hannes M; Balla, Dávid Z; Shajan, G et al. (2016) (17)O relaxation times in the rat brain at 16.4 tesla. Magn Reson Med 75:1886-93
Taylor, Jennifer M; Zhu, Xiao-Hong; Zhang, Yi et al. (2015) Dynamic correlations between hemodynamic, metabolic, and neuronal responses to acute whole-brain ischemia. NMR Biomed 28:1357-65
Wang, Xiao; Zhu, Xiao-Hong; Zhang, Yi et al. (2015) Simultaneous Imaging of CBF Change and BOLD with Saturation-Recovery-T1 Method. PLoS One 10:e0122563
Zhu, Xiao-Hong; Lu, Ming; Lee, Byeong-Yeul et al. (2015) In vivo NAD assay reveals the intracellular NAD contents and redox state in healthy human brain and their age dependences. Proc Natl Acad Sci U S A 112:2876-81
Lu, Ming; Zhu, Xiao-Hong; Zhang, Yi et al. (2014) Intracellular redox state revealed by in vivo (31) P MRS measurement of NAD(+) and NADH contents in brains. Magn Reson Med 71:1959-72
Lu, Ming; Chen, Wei; Zhu, Xiao-Hong (2014) Field dependence study of in vivo brain (31) P MRS up to 16.4?T. NMR Biomed 27:1135-41
Zhu, Xiao-Hong; Chen, James M; Tu, Tsang-Wei et al. (2013) Simultaneous and noninvasive imaging of cerebral oxygen metabolic rate, blood flow and oxygen extraction fraction in stroke mice. Neuroimage 64:437-47

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