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. 2001 Feb 15;21(4):1413–1419. doi: 10.1523/JNEUROSCI.21-04-01413.2001

Table 2.

Effects of chelerythrine on the METH-induced decrease in [3H]DA uptake

Treatment [3H]DA uptake ± SEM
Control 0.64  ± 0.06
10 μm METH 0.31  ± 0.03*
0.1 μm chelerythrine 0.61  ± 0.09
0.1 μm chelerythrine/10 μmMETH 0.29  ± 0.02*
1 μmchelerythrine 0.57  ± 0.08
1 μmchelerythrine/10 μm METH 0.27  ± 0.04*

Striatal synaptosomes were pretreated with 1 or 0.1 μm chelerythrine for 5 min and then preincubated with 10 μm METH or assay buffer for 30 min at 37°C. Before assaying [3H]DA influx, synaptosomal preparations were washed two extra times, as described in Materials and Methods. Values represent means and 1 SEM of determinations from three independent experiments. Values for [3H]DA uptake represent femtomoles per microgram of protein.

*

Values different from respective control groups (p ≤ 0.05).