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. 2007 Sep 5;3(4):285–298. doi: 10.1007/s11302-007-9065-z

Fig. 1.

Fig. 1

Effect of the selective Y1 agonist [F7,P34]pNPY as well as neuropeptide Y (NPY) alone and in combination with selective A1R agonist N6-cyclopentyladenosine (CPA) on the amplitude of postsynaptic potentials (PSPs) evoked by electrical field stimulation (0.2 Hz, 2 ms) in layer I of the rat cingulate cortex (Sichardt et al., unpublished results). Intracellular recordings were performed in rat brain slices using glass microelectrodes placed in pyramidal cells of layer V. a [F7,P34]pNPY superfused for 5 min inhibits reversibly the PSPs by 34.6 ± 8%. Y1 antagonist BIBP3226 itself reduces the PSP by 23 ± 10%, whereas [F7,P34]pNPY has no inhibitory effect in the presence of the antagonist. b NPY depresses PSPs by 28.6 ± 0.7%. The combined superfusion of NPY and CPA resulted in an additional depression of the PSPs by 48.1 ± 5%. The depressant effects of the two agonists were reversible during washout. Data are expressed as mean ± SEM from n = 3 independent experiments. *p < 0.05 significant vs control; #p < 0.05 significant vs NPY alone