Quantification of [(123)I]PE2I binding to dopamine transporters with SPET

Eur J Nucl Med Mol Imaging. 2002 May;29(5):623-31. doi: 10.1007/s00259-001-0742-9. Epub 2002 Mar 1.

Abstract

The iodinated cocaine derivative [(123)I]PE2I is a new selective ligand for in vivo studies of the dopamine transporter (DAT) with single-photon emission tomography (SPET). The aim of the present study was to describe a method for accurate quantification of binding data following a bolus injection of [(123)I]PE2I. Six healthy subjects (age 51+/-24 years) underwent xenon-133 SPET for quantification of regional CBF and [(123)I]PE2I SPET for quantification of DAT binding. rCBFs were within normal limits in all subjects. Fitting data to a two-tissue compartment model resulted in striatal K(1) values of 0.39+/-0.08 ml ml(-1) min(-1), equal to a first-pass extraction fraction of 0.72+/-0.13. Distribution volumes (DVs) were calculated using compartment analysis, area under the curve analysis and Logan analysis. Logan analysis is preferred since stable DV values were already obtained 120 min after [(123)I]PE2I injection. Mean striatal DV was 37.9+/-9.6 ml ml(-1) and mean occipital cortex DV was 5.5+/-0.7 ml ml(-1). In the absence of local pathology in a reference tissue, Logan analysis without blood sampling is an attractive method for accurate quantification of striatal [(123)I]PE2I binding. The distribution volume ratio (DVR) (6.6+/-1.4) was in good agreement with the DVR calculated with blood (6.7+/-1.4).

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Area Under Curve
  • Cerebral Cortex / blood supply
  • Cerebral Cortex / diagnostic imaging
  • Cerebral Cortex / metabolism*
  • Cerebrovascular Circulation
  • Corpus Striatum / blood supply
  • Corpus Striatum / diagnostic imaging
  • Corpus Striatum / metabolism*
  • Dopamine Plasma Membrane Transport Proteins
  • Humans
  • Membrane Glycoproteins*
  • Membrane Transport Proteins / metabolism*
  • Middle Aged
  • Models, Biological*
  • Models, Chemical
  • Nerve Tissue Proteins*
  • Nortropanes / pharmacokinetics*
  • Phantoms, Imaging
  • Radiopharmaceuticals / pharmacokinetics
  • Sensitivity and Specificity
  • Tissue Distribution
  • Tomography, Emission-Computed, Single-Photon
  • Xenon Radioisotopes / pharmacokinetics

Substances

  • Dopamine Plasma Membrane Transport Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • N-(3-iodoprop-2-enyl)-2-beta-carbomethoxy-3-(4-methylphenyl)nortropane
  • Nerve Tissue Proteins
  • Nortropanes
  • Radiopharmaceuticals
  • SLC6A3 protein, human
  • Xenon Radioisotopes