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. 2008 Apr 2;28(14):3567–3576. doi: 10.1523/JNEUROSCI.4679-07.2008

Table 4.

Inhibition of bursting by subtype-selective ligands

Ligand Receptor(s) activated % inhibition of burst rate Number of slices
SST All 58.6 ± 4% 11
Octreotide SST2 > SST3 33.9 ± 4%* 9
l-796,778 SST3 5.2 ± 3.4* , ** 5
J-2156 SST4 21.8 ± 3%* 10
l-803,087 SST4 2.1 ± 5.7%* , ** 8
Octreotide + J-2156 SST2 + SST4 47.0 ± 5 6
SST + SRA880 a All but SST1 47.0 ± 2 7
SST + ACQ090 b All but SST3 46 ± 5 6

Concentration is 1 μm for all drugs except when octreotide and J-2156 are coapplied (0.5 μm each).

aSST1-selective antagonist.

bSST3-selective antagonist.

*Significantly different from SST alone (p < 0.05; unpaired t test);

**no significant inhibition of burst rate (p > 0.05; paired t test).