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. 2018 May 18;126(5):057005. doi: 10.1289/EHP2387

Figure 4.

Figure 4A is a bar graph plotting the percentage of relative c A M P production (y-axis) across concentrations of E2 in 0 to 1 micromolar, and 4 prime OH BDE 049, 5 prime OH BDE 099, and 3 prime OH BDE 154 (x-axis), all measured in 0 to 10 micromolar. Figure 4B is a bar graph plotting the percentage of relative c A M P production (y-axis) across the control group, E2, and 11 OH BDEs (x-axis) in the presence of 10 micromolar G15 and in the absence of G15.

Effects of 17β-estradiol (E2) and 11 hydroxylated polybrominated diphenyl ethers (OH-PBDEs) on cyclic adenosine monophosphate (cAMP) production in SKBR3 cells and the inhibitory effects of G15. (A) cAMP production induced by different concentrations of E2 (0, 0.1nM, 1nM, 10nM, 100nM, and 1μM) and OH-PBDEs (0, 1nM, 10nM, 100nM, 1μM, and 10μM). (B) cAMP production induced by 100nM E2 and 1μM OH-PBDEs in the absence or presence of 10μM G15, a G protein–coupled estrogen receptor antagonist. *p<0.05 compared with the control group (Ctrl, 0.1% dimethyl sulfoxide). #p<0.05 compared with the groups treated with compounds in the absence of G15.