European Journal of Nuclear Medicine and Molecular Imaging

, Volume 37, Issue 8, pp 1594–1603

Recent advances in PET imaging for evaluation of Parkinson’s disease


    • Department of Nuclear MedicineUniversity Hospital of Ioannina
    • Department of Nuclear MedicineUniversity of Ioannina School of Medicine, University Campus
  • Andreas Fotopoulos
    • Department of Nuclear MedicineUniversity Hospital of Ioannina
  • Athanassios P. Kyritsis
    • Department of NeurologyUniversity Hospital of Ioannina
    • Neurosurgical Research InstituteUniversity of Ioannina
Review Article

DOI: 10.1007/s00259-009-1357-9

Cite this article as:
Sioka, C., Fotopoulos, A. & Kyritsis, A.P. Eur J Nucl Med Mol Imaging (2010) 37: 1594. doi:10.1007/s00259-009-1357-9


Parkinson’s disease (PD) consists of loss of pigmented dopamine-secreting neurons in the pars compacta of the midbrain substantia nigra. These neurons project to the striatum (putamen and caudate nucleus) and their loss leads to alterations in the activity of the neural circuits that regulate movement. In a simplified model, two dopamine pathways are involved: the direct pathway, which is mediated through facilitation of the D1 receptors, and the indirect pathway through D2 receptors (inhibitory). Positron emission tomography (PET) tracers to image the presynaptic sites of the dopaminergic system include 6-[18F]FDOPA and 6-[18F]FMT, [11C]dihydrotetrabenazine, [11C]nomifensine and various radiolabelled cocaine derivatives. Postsynaptically, for the dopamine D1 subtype the most commonly used ligands are [11C]SCH 23390 or [11C]NNC 112 and for the D2 subtype [11C]raclopride, [11C]MNPA and [18F]DMFP. PET is a sensitive and specific non-invasive molecular imaging technique that may be helpful for evaluation of PD and its differential diagnosis from other parkinsonian syndromes.


PETDopamineD1 receptorD2 receptorParkinson’s diseaseParkinsonian syndrome

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© Springer-Verlag 2010