Table 1.
Comparison of the KI values of 5 psychostimulants to inhibit human and mouse monoamine transporters.
Drug | Cocaine | Methylphenidate | Amphetamine | Methamphetamine | MDMA |
Human | |||||
hDAT | 0.23 ± 0.03 | 0.06 ± 0.01 | 0.64 ± 0.14 | 0.46 ± 0.06 | 8.29 ± 1.67 |
hNET | 0.48 ± 0.05 | 0.10 ± 0.01 | 0.07 ± 0.01 | 0.11 ± 0.01 | 1.19 ± 0.13 |
hSERT | 0.74 ± 0.03 | 132.43 ± 10.71 | 38.46 ± 3.84 | 31.74 ± 2.40 | 2.41 ± 0.73 |
Ratio 1 | 3.2 | 2207 | 549 | 288 | 7.0 |
Mouse | |||||
mDAT | 0.49 ± 0.04 2 | 0.26 ± 0.03 | 0.56 ± 0.11 | 0.47 ± 0.08 | 4.87 ± 0.65 |
mNET | 0.46 ± 0.06 2 | 0.17 ± 0.03 | 0.12 ± 0.02 | 0.19 ± 0.05 | 1.75 ± 0.51 |
mSERT | 0.73 ± 0.12 | 114.37 ± 7.61 | 23.82 ± 1.71 | 9.28 ± 0.86 | 0.64 ± 0.05 |
Ratio 1 | 1.6 | 672 | 199 | 49 | 7.6 |
The KI values (in μM) were determined as illustrated in Fig. 1. They are expressed as mean ± S.E.M. of four to seven experiments. 1 The ratios of highest KI values over the lowest are shown to highlight the differences. 2 The difference between these two KI values was not statistically significant (ANOVA post hoc Bonferroni test, p > 0.05); all other values were statistically different (ANOVA comparing the three transporters within the same species and for the same drug).