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. 2018 Nov 5;1866(7):1151–1161. doi: 10.1016/j.bbamcr.2018.10.022

Fig. 3.

Fig. 3

Ca2+ channel blockers, dopamine antagonists and selective estrogen receptor modulators block endogenous NAADP-mediated Ca2+ signals.

A, exemplar Ca2+ signals, recorded using Fluo-4 from sea urchin egg homogenates pre-incubated with the indicated drug (100 μM) or DMSO (black traces) for ~1 min prior to stimulation with NAADP (1 μM).

B, concentration-effect relationships for blockade of NAADP responses by the various drugs (n = 3). Data are normalised to the NAADP response in the presence of DMSO.

C, summary data quantifying the effect of the drugs (100 μM) on Ca2+ response to NAADP versus cyclic ADP-ribose (n = 3). Data are normalised to the NAADP and cyclic ADP-ribose responses in the presence of DMSO.