Assessment of cerebral dopamine D-2/3- receptors in patients with bilateral vestibular failure

作者：Jansen Nathalie L; Feuerecker Regina; Becker Bense Sandra; Zwergal Andreas; Wulff Melanie; Xiong Guoming; Waengler Bjoern; Cumming Paul; Bartenstein Peter; Dieterich Marianne^*; la Fougere Christian

来源：Journal of Vestibular Research-Equilibrium & Orientation, 2014, 24(5-6): 403-413.

DOI：10.3233/VES-140526

• [F-18]FP
• PET
• dopamine D-2/3-receptors
• bilateral vestibular failure

BACKGROUND: Absence of peripheral vestibular input in bilateral vestibular failure (BVF) has been suggested to induce plastic reorganization in various brain regions. Among several neurotransmitters, dopamine is known to play a key role in cortico-striatal- sensorimotor processing. However, the role of dopamine in vestibular plasticity is scantly documented.
OBJECTIVE: Assessment of D-2/3-receptors in patients with BVF.
METHODS: D-2/3-receptor-PET using [F-18]fallypride and MRI examinations were performed in 12 BVF-patients and 13 healthy controls.
RESULTS: BVF-patients showed reduced D-2/3-receptor availability (approximately 40%) in the temporo-parieto-occipital cortex bilaterally, including the multisensory vestibular cortex and visual motion-sensitive areas (MT/MST), as well as in the striatum and the right thalamus. Longer illness duration was associated with bilaterally lower D-2/3-receptor availability in the middle/ superior temporal gyrus (GTm/s). D-2/3-receptor availability in the right GTm/s and bilateral insula decreased with severity of symptoms. BVF-patients with oscillopsia showed reduced D-2/3-receptor availability in the right MT/MST and midbrain tectum.
CONCLUSIONS: Reduced D-2/3-receptor availability in multisensory vestibular cortical network areas and basal ganglia may indicate a receptor down-regulation due to the lack of peripheral vestibular input. The more pronounced decline in D-2/3-receptor availability in the multisensory vestibular cortex in patients with prolonged illness suggests the occurrence of progressive changes in dopamine transmission.

• 出版日期2014