A. Buck et al., MONOAMINE-OXIDASE-B SINGLE-PHOTON EMISSION TOMOGRAPHY WITH [I-123] RO-43-0463 - IMAGING IN VOLUNTEERS AND PATIENTS WITH TEMPORAL-LOBE EPILEPSY, European journal of nuclear medicine, 25(5), 1998, pp. 464-470
Imaging of monoamine oxidase of subtype B (MAO B) is of interest in va
rious neurological diseases. In the past non-invasive assessment of MA
O B has only been possible with positron emission tomography (PET) lig
ands. Given the limited availability of PET, 3 single-photon emission
tomography (SPET) ligand would be desirable. In this study SPET imagin
g with the new MAO B inhibitor [I-123]Ro 43-0463 was performed in five
volunteers and nine patients with temporal lobe epilepsy (TLE). In tw
o volunteers a second study was performed 12 h following blockade with
deprenyl. In the TLE patients the tracer was administered as bolus (n
= 4) or as prolonged infusion (n = 5). The regional uptake pattern co
rrelated well with the known distribution of MAO B. In the two blockin
g studies ligand uptake was substantially reduced compared with baseli
ne. In the TLE patients increased uptake was found in the ipsilateral
mesial temporal lobe and, surprisingly, in the ipsilateral putamen. Th
is study indicates the potential of the new SPET ligand [I-123]Ro 43-0
463 to map MAO B concentration in the human brain. The new finding of
in creased MAO B in the putamen of TLE patients needs further studies
to elucidate its exact pathophysiology.