Cerebral blood flow predicts differential neurotransmitter activity

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作者
Juergen Dukart
Štefan Holiga
Christopher Chatham
Peter Hawkins
Anna Forsyth
Rebecca McMillan
Jim Myers
Anne R Lingford-Hughes
David J Nutt
Emilio Merlo-Pich
Celine Risterucci
Lauren Boak
Daniel Umbricht
Scott Schobel
Thomas Liu
Mitul A Mehta
Fernando O Zelaya
Steve C Williams
Gregory Brown
Martin Paulus
Garry D Honey
Suresh Muthukumaraswamy
Joerg Hipp
Alessandro Bertolino
Fabio Sambataro
机构
[1] Roche Innovation Centre Basel,F. Hoffmann
[2] King’s College London,La Roche, pharma Research Early Development
[3] The University of Auckland,Department of Neuroimaging, Institute of Psychiatry, Psychology & Neuroscience
[4] University of California San Diego,School of Pharmacy, Faculty of Medical and Health Sciences
[5] 9500 Gilman Drive MC 0677,Center for Functional MRI
[6] Psychiatry and Bioengineering,Departments of Radiology
[7] University of California San Diego,Institute Of Psychiatry, Department of Basic Medical Science
[8] 9500 Gilman Drive,Department of Experimental and Clinical Medical Sciences (DISM)
[9] University of California,undefined
[10] San Diego,undefined
[11] Veterans Affairs San Diego Healthcare System,undefined
[12] Neuroscience and Sense Organs,undefined
[13] University of Bari ‘Aldo Moro’,undefined
[14] University of Udine,undefined
[15] Neuropsychopharmacology Unit,undefined
[16] Imperial College London,undefined
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摘要
Application of metabolic magnetic resonance imaging measures such as cerebral blood flow in translational medicine is limited by the unknown link of observed alterations to specific neurophysiological processes. In particular, the sensitivity of cerebral blood flow to activity changes in specific neurotransmitter systems remains unclear. We address this question by probing cerebral blood flow in healthy volunteers using seven established drugs with known dopaminergic, serotonergic, glutamatergic and GABAergic mechanisms of action. We use a novel framework aimed at disentangling the observed effects to contribution from underlying neurotransmitter systems. We find for all evaluated compounds a reliable spatial link of respective cerebral blood flow changes with underlying neurotransmitter receptor densities corresponding to their primary mechanisms of action. The strength of these associations with receptor density is mediated by respective drug affinities. These findings suggest that cerebral blood flow is a sensitive brain-wide in-vivo assay of metabolic demands across a variety of neurotransmitter systems in humans.
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