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. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: J Neurochem. 2010 Jul 27;114(6):1781–1791. doi: 10.1111/j.1471-4159.2010.06890.x

Table 1. IC50 and Imax values for inhibition of 1 p evoked [DA]o by the selective D2 receptor agonist quinpirole in non-transgenic (non-Tg), phenotype positive (Phe(+)) and phenotype negative (Phe(−)) mice.

Group IC50 (nM) Imax (%)
Non-Tg 46.7 ± 5.3 96.8 ± 1.1
Phe(−) 35.6 ± 6.3 93.0 ± 1.4
Phe(+) 29.7 ± 5.2* 91.0 ± 2.6
*

IC50 and Imax values were calculated by fitting a one-component sigmoidal curve to concentration-response data from individual experiments and are expressed as means ± SEM (n = 5 per group). The IC50 for DA release inhibition by quinpirole was significantly lower in Phe (+) mice (p < 0.05 vs. non-Tg) indicating enhanced sensitivity for D2 receptor regulation of DA release. See Methods for experimental details.