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Validity and reliability of extrastriatal [C-11]raclopride binding quantification in the living human brain

Svensson, Jonas E. (author)
Karolinska Institutet
Schain, Martin (author)
Copenhagen Univ Hosp, Neurobiol Res Unit, Copenhagen, Denmark.
Plaven-Sigray, Pontus (author)
Karolinska Inst, Ctr Psychiat Res, Dept Clin Neurosci, SE-17176 Stockholm, Sweden.;Karolinska Univ Hosp, Stockholm Cty Council, Stockholm Hlth Care Serv, SE-17176 Stockholm, Sweden.
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Cervenka, Simon (author)
Karolinska Institutet
Tiger, Mikael (author)
Karolinska Institutet
Nord, Magdalena (author)
Karolinska Inst, Ctr Psychiat Res, Dept Clin Neurosci, SE-17176 Stockholm, Sweden.;Karolinska Univ Hosp, Stockholm Cty Council, Stockholm Hlth Care Serv, SE-17176 Stockholm, Sweden.
Halldin, Christer (author)
Karolinska Institutet
Farde, Lars (author)
Karolinska Institutet
Lundberg, Johan (author)
Karolinska Institutet
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Karolinska Institutet Copenhagen Univ Hosp, Neurobiol Res Unit, Copenhagen, Denmark (creator_code:org_t)
ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019
2019
English.
In: NeuroImage. - : ACADEMIC PRESS INC ELSEVIER SCIENCE. - 1053-8119 .- 1095-9572. ; 202
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • [C-11]raclopride is a well established PET tracer for the quantification of dopamine 2/3 receptors (D2/3R) in the striatum. Outside of the striatum the receptor density is up to two orders of magnitude lower. In contrast to striatal binding, the characteristics of extrastriatal [C-11]raclopride binding quantification has not been thoroughly described. Still, binding data for e.g., neocortex is frequently reported in the scientific literature. Here we evaluate the validity and reliability of extrastriatal [C-11]raclopride binding quantification. Two sets of healthy control subjects were examined with HRRT and [C-11]raclopride: (i) To assess the validity of extrastriatal [C-11]raclopride binding estimates, eleven subjects were examined at baseline and after dosing with quetiapine, a D2/3R antagonist. (ii) To assess test-retest repeatability, nine subjects were examined twice. Non displaceable binding potential (BPND) was quantified using the simplified reference tissue model with cerebellum as reference. Quetiapine dosing was associated with decrease in [C-11]raclopride BPND in temporal cortex (18 +/- 17% occupancy) and thalamus (20 +/- 17%), but not in frontal cortex. Extrastriatal occupancy was lower than in putamen (51 +/- 4%). The mean absolute variation was 4-7% in the striatal regions, 17% in thalamus, and 13-59% in cortical regions. Our data indicate that [C-11]raclopride PET, quantified using cerebellum as reference, is not a suitable tool to measure D2/3R in extrastriatal regions.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Radiologi och bildbehandling (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Radiology, Nuclear Medicine and Medical Imaging (hsv//eng)

Keyword

Dopamine
Extrastriatal
Positron emission tomography
Raclopride
Reference region
Occupancy

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