TABLE 2

Specific-to-Nonspecific 123I-FP-CIT Binding Ratios, Obtained 1 and 3 Hours After Injection of Radiotracer, in DAT-Rich Brain Area (Striatum) and in SERT-Rich Areas (Midbrain and Diencephalon)

1 h after injection3 h after injection
123I-FP-CIT BindingPlaceboParoxetine*PlaceboParoxetine
DAT
 Striatum/cer.2.30 ± 0.802.10 ± 0.273.95 ± 0.363.71 ± 0.55
 Striatum/occ.2.95 ± 0.972.93 ± 0.443.97 ± 0.154.41 ± 0.43
SERT
 Midbrain/cer.0.13 ± 0.12−0.04 ± 0.140.21 ± 0.14−0.04 ± 0.05
 Midbrain/occ.0.35 ± 0.100.22 ± 0.170.21 ± 0.120.10 ± 0.06
 Diencephalon/cer.0.29 ± 0.160.08 ± 0.13§0.51 ± 0.170.17 ± 0.15
 Diencephalon/occ.0.54 ± 0.150.38 ± 0.20§0.51 ± 0.100.34 ± 0.13
  • * Placebo or paroxetine tablets (20 mg per session) were taken orally approximately 3 and 27 h before injection of radiotracer.

  • Ratios are expressed as specific to nonspecific binding (±SD). Nonspecific binding represents activity in cerebellum (cer.) or occipital cortex (occ.).

  • Statistically significantly different from placebo condition.

  • § A trend for statistically significant difference (P = 0.07−0.09).

  • Healthy control subjects (n = 5) received placebo or paroxetine before injection of radiotracer (double-blind, crossover study design). In these 5 control subjects, at the paroxetine session, paroxetine plasma levels were >5 μg/L, whereas at the placebo session, paroxetine was not detectable in plasma (<5 μg/L).