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Departments of Nuclear Medicine, Human Genetics and Neurology University of Manitoba, Winnipeg, Canada
Correspondence: For correspondence or reprints contact: Dr. W.D. Leslie, Department of Internal Medicine (C5121), St. Boniface General Hospital, 409 Tache Ave., Winnipeg, Canada R2H 2A6.
ABSTRACT
Although 123I-IBZM is widely used as a D2 receptor imaging agent, image quality is compromised by a relatively low target-to-nontarget ratio. Animal studies suggest that 123I-epidepride (Kd 0.024 n/W) may be superior to 123I-IBZM, but this agent has not been systematically studied in humans. Methods: We directly compared 123I-epidepride and 123I-IBZM in five normal volunteers (age range 3058 yr, mean 43 yr). Brain SPECT imaging was performed 2 hr after the 123I-IBZM injection (average dose 153 MBq). Iodine-123-epidepride scans were performed 1 hr (n = 3), 2 hr (n = 5) and 3 hr (n = 3) postinjection (average dose 149 MBq). Results: Both radiopharmaceuticals were well tolerated, Iodine-123-epidepride provided excellent visualization of the striatum. Percent specific striatum uptake at 2 hr (71.7 ± 4.9%) was much greater than with 123I-IBZM (32.6 ± 5.3%, p < 0.01). Conclusion: Iodine-123-epidepride is a new D2 receptor agent that exhibits excellent neuroimaging properties and has a much higher affinity for striatal uptake than 123I-IBZM.
Key Words: neuroimaging neurotransmitter dopamine
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