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. Author manuscript; available in PMC: 2020 Jan 5.
Published in final edited form as: Eur J Pharmacol. 2018 Oct 25;842:351–364. doi: 10.1016/j.ejphar.2018.10.028

Table 3.

Radioligand uptake inhibition by cocaine, corticosterone, and decynium-22 at mouse DAT, NET, and SERT transiently expressed in HEK cells.

Drug Name mDAT-HEK
IC50 in μM
[95% CI] (n)
mNET-HEK
IC50 in μM
[95% CI] (n)
mSERT-HEK
IC50 in μM
[95% CI](n)
Cocaine 0.18 aaa
[0.095–0.32] (6)
1.18 aaa, bbb
[0.8–1.8] (6)
0.51 aaa
[0.22–1.16] (6)
Corticosterone 364.6 aaa
[154.7–859.4] (6)
839.8 aaa
[334–2113] (6)
444.7 aaa
[128.6–153.8] (6)
Decynium 22ccc 12.9
[9.8–16.9] (6)
35.0bbb
[25–49.2] (6)
7.9 bb
[6.4–9.7] (6)

IC50 estimations determined from concentration response curves (Fig. 4) fit to a nonlinear regression.

a

P < 0.05

aa

P < 0.01

aaa

P < 0.001 indicates significance of difference for the drug versus decynium 22 within a cell line.

b

P < 0.05

bb

P < 0.01

bbb

P < 0.001 indicates significance of difference for the compound compared to mDAT

ccc

P < 0.001 indicates significant difference between mNET and mSERT.