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. 2017 Nov 1;37(44):10671–10678. doi: 10.1523/JNEUROSCI.1971-17.2017

Table 1.

Experimental details

Monkey Weight, kg Inj. mass, μg/kg BPND Drug Drug dose, μg/kg Time of administration, min Induction anesthetics
M1 10.6 0.70 2.15 BSL Type 1
M3 7.4 0.41 2.04 BSL Type 1
M2 11.4 0.13 2.02 AZ 0.88 55.2 Type 1
M1 10.6 0.12 1.91 AZ 0.94 65.5 Type 1
M1 10.6 0.27 2.09 AZ 1.89 52.3 Type 1
M1 10.6 0.12 2.07 AZ 2.86 55.0 Type 1
M3 7.4 0.25 1.94 AZ 4.05 62.4 Type 1
M2 12.0 0.56 1.74 AZ 4.17 60.0 Type 2
M3 10.3 0.34 1.90 AZ 4.85 59.9 Type 2
M2 13.8 0.15 0.88 AZ 5.00 60.0 Type 2
M2 13.8 0.14 0.61 AZ 36.20 40.0 Type 2
AZ 5.00 60.0
M3 10.3 0.37 1.67 Sumatriptan 19.4 59.6 Type 2
M2 12.0 0.30 1.70 GR127935 200 60.0 Type 2
M3 12.2 0.42 1.12 GR127935 200 62.8 Type 2
M3 12.2 0.31 n.a. GR127935 500 −14.0 Type 2
AZ 5.00 60.1

BPND represent the baseline nondisplaceable binding potential before a challenge. BSL indicates a baseline experiment, where no challenge was given. Time of administration of the drug is relative to the injection (inj.) of the radioligand. Induction of anesthesia was performed in two ways: Type 1: diazepam (0.4 mg/kg) + ketamine (20 mg/kg); Type 2: ketamine (10 mg/kg) + xylazine (0.5 mg/kg) following reversal of xylazine with yohimbine (0.11 mg/kg).