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. 2021 Apr 15;11:8288. doi: 10.1038/s41598-021-87417-2

Table 3.

Potency (pEC50) and maximal effect (Emax) estimates for agonists activating D2R G protein signalling pathways.

Agonist i1 oA GIRK
pEC50 Emax pEC50 Emax pEC50 Emax
Dopamine 7.50 ± 0.09 100.0 8.63 ± 0.08 100.0 8.70 ± 0.06 100.0
Apomorphine 8.10 ± 0.07 103.6 ± 2.5 9.07 ± 0.06 98.6 ± 1.9 9.13 ± 0.08 110.0 ± 3.5
Aripiprazole 6.21 ± 0.17 67.5 ± 6.9 6.64 ± 0.08 97.6 ± 3.8 ND ND
Bromocriptine 7.07 ± 0.08 115.0 ± 4.1 7.84 ± 0.05 103.7 ± 2.0 7.38 ± 0.08 104.7 ± 4.3
Cabergoline 8.13 ± 0.16 109.8 ± 6.5 8.80 ± 0.05 102.7 ± 1.7 9.01 ± 0.08 104.0 ± 3.4
MLS1547 5.71 ± 0.20 123.9 ± 19.5 6.68 ± 0.08 106.5 ± 4.4 ND ND
Pergolide 7.73 ± 0.17 112.3 ± 7.3 8.73 ± 0.07 96.7 ± 2.3 9.28 ± 0.07 97.9 ± 2.7
Quinpirole 7.81 ± 0.10 119.3 ± 4.6 8.93 ± 0.05 97.4 ± 1.5 8.98 ± 0.05 104.9 ± 2.1
Ropinirole 7.33 ± 0.13 98.01 ± 5.2 8.55 ± 0.13 93.9 ± 3.7 8.23 ± 0.07 94.4 ± 3.4
Roxindole 8.19 ± 0.12 86.6 ± 4.2 9.04 ± 0.04 90.7 ± 1.1 9.26 ± 0.06 89.7 ± 2.2
Terguride 7.76 ± 0.18 66.2 ± 4.6 8.36 ± 0.05 100.1 ± 1.6 8.05 ± 0.08 53.3 ± 2.1
UNC9994 5.74 ± 0.21 81.6 ± 13.4 6.55 ± 0.08 98.0 ± 4.1 ND ND

Concentration–response curves from Fig. 5 were analyzed using a three-parameter fit (Eq. 1). Values represent the mean ± SEM. ND Not determined: unable to be determined due to insufficient response to allow accurate fitting of the model.