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. 2010 Mar;77(3):327–338. doi: 10.1124/mol.109.061440

TABLE 4.

Relative agonist rank order of efficacy for IP accumulation, Ca2+ release, and ERK1/2 phosphorylation in WT and RSK2 KO MEFs

Letters in parentheses indicate group assignment. Mean relative efficacies were analyzed via one-way ANOVA, and significant differences were determined via the Tukey-Kramer multiple comparison post-test (significance set at p < 0.05). Agonists were arranged in descending order (i.e. 1 through 9) and placed into statistically homogeneous groups (i.e., a through f) such that significant differences in rank order are denoted by changes in group membership. Agonists with nonoverlapping group assignments were considered to be significantly different.

Rank Order IP Accumulation
Ca2+ Release
ERK1/2 Phosphorylation
WT MEFs RSK2 KO MEFs WT MEFs RSK2 KO MEFs WT MEFs RSK2 KO MEFs
1 5-HT (a) 5-Methoxy DMT (a) a-Me5-HT (a) a-Me5-HT (a) Quipazine (a) DOI (a)
2 a-Me5-HT (a,b) Quipazine (a) 5-HT (a,b) 5-HT (a) m-CPP (a) 5-Methoxy DMT (a)
3 Quipazine (b,c) DOI (a,b) Quipazine (a,b,c) MK212 (a) 5-HT (a) a-Me5-HT (a,b)
4 MK212 (c) 5-HT (a) DOI (a,b,c) Quipazine (a,b) DOI (a,b) 5-HT (a)
5 DOI (c,d) MK212 (b,c) 5-Methoxy DMT (b,c,d) 5-Methoxy DMT (a,b,c) Lisuride (a,b) Lisuride (a,b)
6 5-Methoxy DMT (d) a-Me5-HT (c) MK212 (c,d) DOI (a,b,c) 5-Methoxy DMT (a,b) Quipazine (a,b)
7 m-CPP (e) m-CPP (c,d) m-CPP (d) m-CPP (a,b,c) a-Me5-HT (a,b,c) MK212 (a,b)
8 Lisuride (e,f) Lisuride (d) Lisuride (e) Lisuride (b,c) MK212 (b,c) m-CPP (a,b)
9 SCH-23390 (f) SCH-23390 (d) SCH-23390 (e) SCH-23390 (c) SCH-23390 (c) SCH-23390 (b)