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. 2007 Jun 27;27(26):7054–7069. doi: 10.1523/JNEUROSCI.1744-07.2007

Table 5.

The effects of DA are diminished by Na+ channel blockers but not by blockers of other voltage-gated ion channels

Drug Condition αPSP summation
−70 mV −55 mV
TTX (1 μm) (n = 9) Baseline 1.37 ± 0.14 2.35 ± 0.15
TTX 1.33 ± 0.2 0.76 ± 0.07*
+DA 1.10 ± 0.2 0.80 ± 0.20
4-AP (3 mm) (n = 7) Baseline 1.47 ± 0.18 2.14 ± 0.2
4-AP 1.68 ± 0.20* 4.63 ± 0.21*
+DA 1.61 ± 0.20 5.07 ± 0.2*
BaCl2 (250 μm) (n = 6) Baseline 1.42 ± 0.17 2.37 ± 0.16
BaCl2 1.72 ± 0.18* 2.98 ± 0.17*
+DA 1.75 ± 0.17 3.32 ± 0.18*
ZD7288 (20 μm) (n = 7) Baseline 1.49 ± 0.15 2.28 ± 0.2
ZD7288 1.89 ± 0.18* 2.31 ± 0.2
+DA 2.02 ± 0.16 2.79 ± 0.2*
NiCl2/nimodipine (50/10 μm) (n = 6) Baseline 1.55 ± 0.19 2.38 ± 0.2
NiCl2/nim 1.61 ± 0.18 2.44 ± 0.17
+DA 1.57 ± 0.21 2.96 ± 0.18*

Application of DA causes an increase in PSP summation at depolarized membrane potentials, even when blockers of K+, Ca2+, or h-channels are present. *p < 0.05 (paired t test) compared with previous condition at the same voltage.