SINGLE-PHOTON EMISSION TOMOGRAPHY (SPET) IMAGING OF DOPAMINE D-2 RECEPTORS IN THE COURSE OF DOPAMINE REPLACEMENT THERAPY IN PATIENTS WITH NOCTURNAL MYOCLONUS SYNDROME (NMS)
J. Staedt et al., SINGLE-PHOTON EMISSION TOMOGRAPHY (SPET) IMAGING OF DOPAMINE D-2 RECEPTORS IN THE COURSE OF DOPAMINE REPLACEMENT THERAPY IN PATIENTS WITH NOCTURNAL MYOCLONUS SYNDROME (NMS), Journal of neural transmission, 99(1-3), 1995, pp. 187-193
Single photon emission tomography (SPET) permits the in vivo measureme
nts of regional cerebral radioactivity in the human brain following th
e administration of compounds labeled with photon-emitting isotopes. A
ccording to our SPET findings of a reduced binding of [I-123]labeled -
3-iodo-6-methoxy-([1-ethyl-2-pyrrolidinyl]methyl) benzamide (IBZM) (a
highly selective CNS D-2 dopamine receptor ligand) to D-2 dopamine rec
eptors in striatal structures in untreated patients with nocturnal myo
clonus syndrome (NMS) it seemed to be of interest to investigate wheth
er there are changes in D-2 receptor binding under dopamine replacemen
t therapy or not. We studied the uptake and distribution of [I-123]IBZ
M before and in the course of dopamine replacement therapy in four pat
ients with severe insomnia caused by a nocturnal myoclonus syndrome (N
MS). We found an increase of the IBZM binding to D-2 receptors in the
course of treatment, which was associated with an improvement of sleep
quality. Reasons for this are discussed. The [I-123]IBZM SPET techniq
ue in conclusion offers an interesting tool for in vivo investigations
of functional changes in the dopaminergic neurotransmitter system in
longitudinal studies.