A) Electrophysiological recordings were performed from
CRF1+ labeled neurons in CeA slices. B) Representative
traces of mIPSCs at baseline, in the presence of R121219 (1 μM) and
MLS-0046818 (30 μM), and R121219 (1 μM) + MLS-0046818 (30
μM) + CRF (200 nM). C) Application of R121219 (1 μM) and
MLS-0046818 (30 μM) for 15 min does not induce significant changes: one
sample t-test, p = 0.5575 (frequency),
p = 0.0908 (amplitude), p = 0.2017 (rise
time) and p = 0.4208 (decay) in mIPSC properties relative to
baseline (one-sample t-test; n = 9 neurons/6
mice). D) Application of CRF (200 nM) following pre-treatment of brain slices
with R121219 (1 μM) and MLS-0046818 (30 μM) for 15 min do not
produce significant changes: one sample t-test,
p = 0.8948 (frequency), p = 0.3619
(amplitude), p = 0.7754 (rise time) and p =
0.1513 (decay) in mIPSC properties relative to baseline (one-sample t-test,
n = 8 neurons/4 mice).