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. 2004 Feb 2;141(4):737–745. doi: 10.1038/sj.bjp.0705652

Figure 1.

Figure 1

[Ca2+]i responses to TRPM8 agonists. [Ca2+]i fluxes induced by icilin (5 μM), WS-3 (30 μM), (−)menthol (30 μM) and eucalyptol (5 mM) were monitored using the FLIPR® assay in mTRPM8-transfected HEK293 cells. [Ca2+]i responses were measured as changes in fluorescence intensity (FI) before and after the addition of agonists. The data shown are representative plots of the fluorescence signals against time during assays.