Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI

This study employed simultaneous neuroimaging with positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) to demonstrate the relationship between changes in receptor occupancy measured by PET and changes in brain activity inferred by fMRI. By administering the D2/D3 dopa...

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Main Authors: Sander, Christin Yen-Ming, Rosen, Bruce R., Hooker, Jacob M., Catana, Ciprian, Normandin, Marc D., Alpert, Nathaniel M., Knudsen, Gitte M., Vanduffel, Wim, Mandeville, Joseph B.
Other Authors: Harvard University--MIT Division of Health Sciences and Technology
Format: Article
Language:en_US
Published: National Academy of Sciences (U.S.) 2014
Online Access:http://hdl.handle.net/1721.1/85908
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author Sander, Christin Yen-Ming
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
Normandin, Marc D.
Alpert, Nathaniel M.
Knudsen, Gitte M.
Vanduffel, Wim
Mandeville, Joseph B.
author2 Harvard University--MIT Division of Health Sciences and Technology
author_facet Harvard University--MIT Division of Health Sciences and Technology
Sander, Christin Yen-Ming
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
Normandin, Marc D.
Alpert, Nathaniel M.
Knudsen, Gitte M.
Vanduffel, Wim
Mandeville, Joseph B.
author_sort Sander, Christin Yen-Ming
collection MIT
description This study employed simultaneous neuroimaging with positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) to demonstrate the relationship between changes in receptor occupancy measured by PET and changes in brain activity inferred by fMRI. By administering the D2/D3 dopamine receptor antagonist [[superscript 11]C]raclopride at varying specific activities to anesthetized nonhuman primates, we mapped associations between changes in receptor occupancy and hemodynamics [cerebral blood volume (CBV)] in the domains of space, time, and dose. Mass doses of raclopride above tracer levels caused increases in CBV and reductions in binding potential that were localized to the dopamine-rich striatum. Moreover, similar temporal profiles were observed for specific binding estimates and changes in CBV. Injection of graded raclopride mass doses revealed a monotonic coupling between neurovascular responses and receptor occupancies. The distinct CBV magnitudes between putamen and caudate at matched occupancies approximately matched literature differences in basal dopamine levels, suggesting that the relative fMRI measurements reflect basal D2/D3 dopamine receptor occupancy. These results can provide a basis for models that relate dopaminergic occupancies to hemodynamic changes in the basal ganglia. Overall, these data demonstrate the utility of simultaneous PET/fMRI for investigations of neurovascular coupling that correlate neurochemistry with hemodynamic changes in vivo for any receptor system with an available PET tracer.
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spelling mit-1721.1/859082022-10-01T03:33:37Z Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI Sander, Christin Yen-Ming Rosen, Bruce R. Hooker, Jacob M. Catana, Ciprian Normandin, Marc D. Alpert, Nathaniel M. Knudsen, Gitte M. Vanduffel, Wim Mandeville, Joseph B. Harvard University--MIT Division of Health Sciences and Technology Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Sander, Christin Yen-Ming Rosen, Bruce R. This study employed simultaneous neuroimaging with positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) to demonstrate the relationship between changes in receptor occupancy measured by PET and changes in brain activity inferred by fMRI. By administering the D2/D3 dopamine receptor antagonist [[superscript 11]C]raclopride at varying specific activities to anesthetized nonhuman primates, we mapped associations between changes in receptor occupancy and hemodynamics [cerebral blood volume (CBV)] in the domains of space, time, and dose. Mass doses of raclopride above tracer levels caused increases in CBV and reductions in binding potential that were localized to the dopamine-rich striatum. Moreover, similar temporal profiles were observed for specific binding estimates and changes in CBV. Injection of graded raclopride mass doses revealed a monotonic coupling between neurovascular responses and receptor occupancies. The distinct CBV magnitudes between putamen and caudate at matched occupancies approximately matched literature differences in basal dopamine levels, suggesting that the relative fMRI measurements reflect basal D2/D3 dopamine receptor occupancy. These results can provide a basis for models that relate dopaminergic occupancies to hemodynamic changes in the basal ganglia. Overall, these data demonstrate the utility of simultaneous PET/fMRI for investigations of neurovascular coupling that correlate neurochemistry with hemodynamic changes in vivo for any receptor system with an available PET tracer. National Institutes of Health (U.S.) (Grant R90DA023427) National Institutes of Health (U.S.) (Grant P41RR14075) National Institutes of Health (U.S.) (Grant P30DA28800) National Institutes of Health (U.S.) (Grant S10RR026666) National Institutes of Health (U.S.) (Grant S10RR017208) National Institutes of Health (U.S.) (Grant S10RR022976) National Institutes of Health (U.S.) (Grant S10RR019933) 2014-03-24T16:48:46Z 2014-03-24T16:48:46Z 2013-07 2012-12 Article http://purl.org/eprint/type/JournalArticle 0027-8424 1091-6490 http://hdl.handle.net/1721.1/85908 Sander, C. Y., J. M. Hooker, C. Catana, M. D. Normandin, N. M. Alpert, G. M. Knudsen, W. Vanduffel, B. R. Rosen, and J. B. Mandeville. “Neurovascular Coupling to D2/D3 Dopamine Receptor Occupancy Using Simultaneous PET/functional MRI.” Proceedings of the National Academy of Sciences 110, no. 27 (July 2, 2013): 11169–11174. en_US http://dx.doi.org/10.1073/pnas.1220512110 Proceedings of the National Academy of Sciences Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf National Academy of Sciences (U.S.) National Academy of Science (U.S.)
spellingShingle Sander, Christin Yen-Ming
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
Normandin, Marc D.
Alpert, Nathaniel M.
Knudsen, Gitte M.
Vanduffel, Wim
Mandeville, Joseph B.
Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title_full Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title_fullStr Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title_full_unstemmed Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title_short Neurovascular coupling to D2/D3 dopamine receptor occupancy using simultaneous PET/functional MRI
title_sort neurovascular coupling to d2 d3 dopamine receptor occupancy using simultaneous pet functional mri
url http://hdl.handle.net/1721.1/85908
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