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. 2008 Jul 30;28(31):7919–7928. doi: 10.1523/JNEUROSCI.0784-08.2008

Figure 7.

Figure 7.

IP3Rs and RyRs contribute to CICR in glycinergic amacrine cells. A, Feedback IPSC before and after bath application of thapsigargin (1 μm). B, Summarized effects (mean ± SD) of thapsigargin (1 μm), RR (40 μm), 2-APB (50 μm), and xestospongin C (XeC; 3 μm) on IPSCs. ND, Experiment not done. C, IPSCs recorded under control conditions, in the presence of Cd2+ and the additional presence of RR. D, IPSCs recorded under control conditions, in the presence of CPP and the additional presence of the RR. E, F, As in C and D, but with the IP3R antagonist 2-APB. G, H, Summarized data (mean ± SD) showing that IP3Rs and RyRs amplify specifically NMDAR-mediated and Cav channel-mediated Ca2+ signals, respectively. All experiments were performed in the presence of GABAR antagonists (SR95531 and TPMPA).