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. 2006 Mar 3;6:6. doi: 10.1186/1471-2210-6-6

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).