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. Author manuscript; available in PMC: 2012 Oct 15.
Published in final edited form as: Biol Psychiatry. 2011 Jul 23;70(8):712–719. doi: 10.1016/j.biopsych.2011.06.010

Table 1.

Noradrenergic (α, β), imidazoline (I1) and corticotropin-releasing factor (CRF R1) receptor ligands used in the current studies.

Drug Receptor action Doses (mg/kg) Vehicle
Clonidine I1> α2 agonist (4-fold) 0.005, 0.01, 0.02 Saline
RS-79948 α2 antagonist (selective) 1.0 Saline
UK-14,304 α2> I1 agonist (100-fold) 0.05, 0.1, 0.2 Water
Guanfacine α2A agonist (selective) 0.2, 1.0 Saline
Moxonidine I1> α2 agonist (40-fold) 0.2, 1.0 Saline
Prazosin α1 (and α2B) antagonist 1.0, 3.0 10% DMSO in water
(S)-(-)-Propranolol β antagonist 5, 10 Saline; (R)-(-)-Prop control
CP-154,526 CRF R1 antagonist 20 5% cremophor in saline
Antalarmin CRF R1 antagonist 10, 20 10% cremophor in water