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. 2010 May 13;21(1):212–221. doi: 10.1093/cercor/bhq081

Figure 5.

Figure 5.

α1 Receptors produce a decrease in LI-eIPSCs amplitude. Averaged time course of the effect of adrenergic agonists and antagonists on eIPSCs. (A) Temporal course showing that the α1 adrenoceptor blocker prazosin (1 μM) blocks the effects of NE. (B) The antagonists for β and α2 receptors (propranolol and yohimbine, 1 μM) did not block the NE action on LI-eIPSCs, suggesting that α1 receptors activation modulated LI-eIPSCs. (C) Phenylephrine (1 μM) decreases LI-eIPSCs amplitude. (D) Previous application of prazosin blocked LI-eIPSCs reduction by the selective α1 noradrenergic receptor (phenylephrine 1 μM). (E) Summary of results with agonists and antagonists indicating that α1 receptors are responsible for NE-induced reduction in LI-eIPSCs amplitude.