Journal
JOURNAL OF NUCLEAR MEDICINE
Volume 57, Issue 6, Pages 950-953Publisher
SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.115.169615
Keywords
MPTP-monkey; dopamine transporter; dopamine synthesis; mitochondria complex l
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F-18-BCPP-EF was applied to assess mitochondrial complex I (MC-I) activity in the brains of Parkinson disease model monkeys prepared by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and also presynaptic dopamine parameters. Methods: C-11-beta-CFT for the dopamine transporter; C-11-3,4-dihydroxy-phenyl-L-alanine (beta-C-11-L-DOPA), L-6-F-18-fluorodopa (F-18-FDOPA), or 6-C-11-methyl-m-tyrosine (C-11-6MemTyr) for dopamine synthesis; or 2-tert-butyl-4-chrolo5-{6-[2-(2-F-18-fluoroethoxy)-ethoxy]-pyridin-3-ylmethoxy}-2H-pyridazin-3-one (F-18-BCPP-EF) for MC-I was intravenously injected into normal and MPTP monkeys in order to analyze their uptake in the striatum. Results: Significant reductions in presynaptic dopamine parameters and MC-I activity were detected in the striatum of MPTP monkeys. Correlations were observed between MC-I activity and dopamine transporter as well as between MC-I activity and dopamine synthesis in the striatum. The order of detectability of impaired MC-I activity was C-11-6MemTyr >> beta-C-11-L-DOPA > F-18-FDOPA. Conclusion: F-18-BCPP-EF has potential as a PET probe for the quantitative imaging of MC-I damage in the living brains of Parkinson disease model monkeys using PET.
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