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. 2014 Jun 12;2(4):e00057. doi: 10.1002/prp2.57

Table 12.

ED50s (95% confidence limits) for inhibition of d-amphetamine-induced hyperlocomotion and for reversal of hypolocomotion induced by the D1 antagonist SCH-23390, the monoamines-depleting agent RO-4-1284, or the D2 antagonist haloperidol measured in mice 0.5 h after s.c. injection

ED50s (95% confidence limits; mg/kg, s.c., −0.5 h)

Compound d-Amphetamine (<5500 cm) SCH-23390 (>2500 cm) RO-4-1284 (>2500 cm) Haloperidol (>2500 cm)
JNJ-42314415 8.1 (5.4–12.2) 7.1 (4.8–10.7) 2.69 (1.99–3.6) >401
PQ-10 12.4 (9.1–16.7) 16.3 (10.1–26.3) 5.4 (–) >40
MP-10 1.78 (1.10–2.87) 1.17 (0.86–1.58) 0.58 (0.34–1.01) >40
TP-10 1.78 (1.19–2.66) 1.78 (1.18–2.65) No stock >10
Haloperidol 0.112 (0.075–0.168)
SKF-82958 0.148 (0.109–0.200) 0.294 (0.218–0.40) >10
1

60% responders at 10 mg/kg.