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. 2014 Dec 31;113(6):1697–1711. doi: 10.1152/jn.00752.2014

Table 1.

Similar D1 agonism-induced enhancement of dorsal striatum-evoked, middle striatum-evoked, and local SNr-evoked striatonigral IPSCs

Mice Bath-applied D1R Agonist Dorsal Striatum-evoked Striatonigral IPSC (C), %increase Middle Striatum-evoked Striatonigral IPSC (D), % increase Ventral Striatum-evoked Striatonigral IPSC (E), % increase Local SNr-evoked Striatonigral IPSC (F), % increase
Pitx3WT (A) SKF81297 (1 μM) 49.9 ± 8.4* 43.3 ± 5.3 46.5 ± 10.0 41.4 ± 7.2
Pitx3Null (B) SKF81297 (1 μM) 94.1 ± 7.2 95.3 ± 14.2 94.7 ± 6.8 75.4 ± 4.8

WT, wild type; D1R, D1 receptor; IPSC, inhibitory postsynaptic current; SNr, substantia nigra pars reticulata.

*

C vs. D vs. E vs. F: P > 0.5;

C vs. D vs. E vs. F: P > 0.1;

A vs. B: P < 0.01: one-way ANOVA followed by post hoc least significant difference test.