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. 2012 Jun 20;32(25):8532–8544. doi: 10.1523/JNEUROSCI.0337-12.2012

Table 2.

VU0364572 and VU0357017 induce Ca responses in hM1 TREx CHO cells treated across a range of TET concentrations

TET concentration CCh
VU0364572
VU0357017
EC 50 (in μm) % CCh max EC 50 (in μm) % CCh max EC 50 (in μm) % CCh max
0 ng/ml (n =3) 2.46 (0.72) 100 (3.45) 30.5 (12.5) 44.2 (9.58) NA 8.24 (5.06)
10 ng/ml (n =3) 2.94 (0.82) 100 (12.8) 146 (120) 39.9 (13.5) 16 (11) 7.21 (6.24)
25 ng/ml (n =3) 1.99 (0.69) 100 (6.40) 2.3 (1.7) 68.1 (13.6) 16 (14) 24.5 (5.53)
50 ng/ml (n =3) 1.08 (0.84) 100 (2.93) 1.0 (0.4) 78.1 (5.95) 1.6 (0.57) 60.4 (11.1)
1 μg/ml (n =3) 0.06 (0.01) 100 (1.29) 0.5 (0.1) 86.2 (3.75) 0.69 (0.24) 75.3 (1.07)

CCh induces a near maximum response in untreated cells. A decrease in the potency values was present in cells treated with 50 or 1 μg of TET suggesting the presence of receptor reserves. In cells treated 25, 50, or 1 μg TET, VU0364572 and VU0357017 induces an increase in Emax values. Both compounds were found to be more potent following treatment of cells across a range of TET concentrations. Values in parentheses are SEM.