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. 2013 Apr 25;169(2):400–412. doi: 10.1111/bph.12116

Figure 3.

Figure 3

Radioligand binding showing the specific binding of [H3]-BK (A) and [H3]-DALBK (B) to human gingival fibroblasts. Cells were pre-incubated for 24 h with either control media or media containing IL-4 (30 ng·mL−1), IL-1β (100 pg·mL−1) without or with IL-4 or TNF-α (25 ng·mL−1) without or with IL-4. Then, the cells were challenged with radiolabelled ligands for 90 min. Values represent means ± SEM of cell bound radioactivity for four wells per group. In figures (C) and (D) is shown the increase in transient [Ca2+]i concentration in response to BK (C) or DALBK (D). Human gingival fibroblasts were pre-incubated without (Ctrl) or with IL-1β (100 pg·mL−1) in the absence of presence of IL-4 (30 ng·mL−1) for 24 h. Then the cells were challenged with the B1 and B2 receptor agonists (1 μM) and intracellular calcium levels were followed by recording the fluorescence intensity. Values represent means ± SEM for 5–10 recordings. The statistically significant effects are shown by asterisks (**, P < 0.01; ***, P < 0.001).