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024 7 _ |a 10.1093/brain/awt263
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024 7 _ |a pmid:24163364
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024 7 _ |a pmc:PMC4125626
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024 7 _ |a 0006-8950
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024 7 _ |a 1460-2156
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037 _ _ |a DZNE-2020-03419
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a del Campo, Natalia
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|e Corresponding author
245 _ _ |a A positron emission tomography study of nigro-striatal dopaminergic mechanisms underlying attention: implications for ADHD and its treatment.
260 _ _ |a Oxford
|c 2013
|b Oxford Univ. Press
264 _ 1 |3 online
|2 Crossref
|b Oxford University Press (OUP)
|c 2013-10-25
264 _ 1 |3 print
|2 Crossref
|b Oxford University Press (OUP)
|c 2013-11-01
336 7 _ |a article
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Through the combined use of (18)F-fallypride positron emission tomography and magnetic resonance imaging this study examined the neural mechanisms underlying the attentional deficits associated with attention deficit/hyperactivity disorder and their potential reversal with a single therapeutic dose of methylphenidate. Sixteen adult patients with attention deficit/hyperactivity disorder and 16 matched healthy control subjects were positron emission tomography and magnetic resonance imaging scanned and tested on a computerized sustained attention task after oral methylphenidate (0.5 mg/kg) and placebo administration in a within-subject, double-blind, cross-over design. Although patients with attention deficit/hyperactivity disorder as a group showed significant attentional deficits and reduced grey matter volume in fronto-striato-cerebellar and limbic networks, they had equivalent D2/D3 receptor availability and equivalent increases in endogenous dopamine after methylphenidate treatment to that observed in healthy control subjects. However, poor attentional performers drawn from both the attention deficit/hyperactivity disorder and the control groups had significantly reduced left caudate dopamine activity. Methylphenidate significantly increased dopamine levels in all nigro-striatal regions, thereby normalizing dopamine levels in the left caudate in low performers. Behaviourally, methylphenidate improved sustained attention in a baseline performance-dependent manner, irrespective of diagnosis. This finding was accompanied by an equally performance-dependent effect of the drug on dopamine release in the midbrain, whereby low performers showed reduced dopamine release in this region. Collectively, these findings support a dimensional model of attentional deficits and underlying nigro-striatal dopaminergic mechanisms of attention deficit/hyperactivity disorder that extends into the healthy population. Moreover, they confer midbrain dopamine autoreceptors a hitherto neglected role in the therapeutic effects of oral methylphenidate in attention deficit/hyperactivity disorder. The absence of significant case-control differences in D2/D3 receptor availability (despite the observed relationships between dopamine activity and attention) suggests that dopamine dysregulation per se is unlikely to be the primary cause underlying attention deficit/hyperactivity disorder pathology in adults. This conclusion is reinforced by evidence of neuroanatomical changes in the same set of patients with attention deficit/hyperactivity disorder.
536 _ _ |a 344 - Clinical and Health Care Research (POF3-344)
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588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Benzamides
|2 NLM Chemicals
650 _ 7 |a Dopamine Uptake Inhibitors
|2 NLM Chemicals
650 _ 7 |a Radiopharmaceuticals
|2 NLM Chemicals
650 _ 7 |a Fluorodeoxyglucose F18
|0 0Z5B2CJX4D
|2 NLM Chemicals
650 _ 7 |a Methylphenidate
|0 207ZZ9QZ49
|2 NLM Chemicals
650 _ 7 |a fallypride
|0 G9FWZ369GX
|2 NLM Chemicals
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Attention Deficit Disorder with Hyperactivity: drug therapy
|2 MeSH
650 _ 2 |a Attention Deficit Disorder with Hyperactivity: metabolism
|2 MeSH
650 _ 2 |a Attention Deficit Disorder with Hyperactivity: pathology
|2 MeSH
650 _ 2 |a Attention Deficit Disorder with Hyperactivity: physiopathology
|2 MeSH
650 _ 2 |a Benzamides
|2 MeSH
650 _ 2 |a Corpus Striatum: drug effects
|2 MeSH
650 _ 2 |a Corpus Striatum: metabolism
|2 MeSH
650 _ 2 |a Corpus Striatum: pathology
|2 MeSH
650 _ 2 |a Corpus Striatum: physiopathology
|2 MeSH
650 _ 2 |a Cross-Over Studies
|2 MeSH
650 _ 2 |a Dopamine Uptake Inhibitors: administration & dosage
|2 MeSH
650 _ 2 |a Dopamine Uptake Inhibitors: pharmacology
|2 MeSH
650 _ 2 |a Double-Blind Method
|2 MeSH
650 _ 2 |a Fluorodeoxyglucose F18
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging: instrumentation
|2 MeSH
650 _ 2 |a Magnetic Resonance Imaging: methods
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Mesencephalon: drug effects
|2 MeSH
650 _ 2 |a Mesencephalon: metabolism
|2 MeSH
650 _ 2 |a Mesencephalon: pathology
|2 MeSH
650 _ 2 |a Mesencephalon: physiopathology
|2 MeSH
650 _ 2 |a Methylphenidate: administration & dosage
|2 MeSH
650 _ 2 |a Methylphenidate: pharmacology
|2 MeSH
650 _ 2 |a Multimodal Imaging: instrumentation
|2 MeSH
650 _ 2 |a Multimodal Imaging: methods
|2 MeSH
650 _ 2 |a Positron-Emission Tomography: instrumentation
|2 MeSH
650 _ 2 |a Positron-Emission Tomography: methods
|2 MeSH
650 _ 2 |a Psychiatric Status Rating Scales
|2 MeSH
650 _ 2 |a Radiopharmaceuticals
|2 MeSH
650 _ 2 |a Young Adult
|2 MeSH
700 1 _ |a Fryer, Tim D
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700 1 _ |a Hong, Young T
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700 1 _ |a Smith, Rob
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700 1 _ |a Brichard, Laurent
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700 1 _ |a Acosta-Cabronero, Julio
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700 1 _ |a Chamberlain, Samuel R
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700 1 _ |a Tait, Roger
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700 1 _ |a Izquierdo, David
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700 1 _ |a Regenthal, Ralf
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700 1 _ |a Dowson, Jonathan
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700 1 _ |a Suckling, John
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700 1 _ |a Baron, Jean-Claude
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700 1 _ |a Aigbirhio, Franklin I
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700 1 _ |a Robbins, Trevor W
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700 1 _ |a Sahakian, Barbara J
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700 1 _ |a Müller, Ulrich
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773 1 8 |a 10.1093/brain/awt263
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|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/S0006-3223(97)00448-4
999 C 5 |a 10.1523/JNEUROSCI.14-01-00088.1994
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.14-01-00088.1994
999 C 5 |a 10.4088/JCP.09m05305whi
|9 -- missing cx lookup --
|2 Crossref
|o 10.4088/JCP.09m05305whi
999 C 5 |a 10.1038/sj.npp.1300534
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/sj.npp.1300534
999 C 5 |a 10.1192/bjp.bp.107.048827
|9 -- missing cx lookup --
|2 Crossref
|o 10.1192/bjp.bp.107.048827
999 C 5 |a 10.1002/syn.20734
|9 -- missing cx lookup --
|2 Crossref
|o 10.1002/syn.20734
999 C 5 |a 10.1037/0033-2909.95.3.387
|9 -- missing cx lookup --
|2 Crossref
|o 10.1037/0033-2909.95.3.387
999 C 5 |a 10.1016/S0002-7138(09)60604-X
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/S0002-7138(09)60604-X
999 C 5 |a 10.1016/S0166-4328(97)00175-7
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/S0166-4328(97)00175-7
999 C 5 |a 10.1016/j.biopsych.2006.07.032
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/j.biopsych.2006.07.032
999 C 5 |a 10.1111/j.1469-8986.1984.tb00247.x
|9 -- missing cx lookup --
|2 Crossref
|o 10.1111/j.1469-8986.1984.tb00247.x
999 C 5 |a 10.1007/s00213-005-0025-4
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00213-005-0025-4
999 C 5 |a 10.1007/s00213-004-1993-5
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00213-004-1993-5
999 C 5 |a 10.1007/s00213-003-1457-3
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00213-003-1457-3
999 C 5 |a 10.1006/nimg.2001.0978
|9 -- missing cx lookup --
|2 Crossref
|o 10.1006/nimg.2001.0978
999 C 5 |a 10.1016/j.neuroimage.2006.10.013
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/j.neuroimage.2006.10.013
999 C 5 |a 10.1176/appi.ajp.163.3.359
|9 -- missing cx lookup --
|2 Crossref
|o 10.1176/appi.ajp.163.3.359
999 C 5 |a 10.1038/npp.2012.127
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/npp.2012.127
999 C 5 |a 10.1001/jama.2009.1308
|9 -- missing cx lookup --
|2 Crossref
|o 10.1001/jama.2009.1308
999 C 5 |a 10.1016/j.neuroimage.2006.10.014
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/j.neuroimage.2006.10.014
999 C 5 |a 10.1001/archpsyc.64.8.932
|9 -- missing cx lookup --
|2 Crossref
|o 10.1001/archpsyc.64.8.932
999 C 5 |a 10.1038/376572a0
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/376572a0


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21