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. 2011 Jan;162(2):378–391. doi: 10.1111/j.1476-5381.2010.01021.x

Figure 5.

Figure 5

In vitro model of homologous β2-adrenoceptor desensitization. (A) Concentration–response curves for salbutamol in human bronchial smooth muscle cells treated with vehicle (Ctrl) or homologously desensitized (Des) with salbutamol 1 µmol·L−1 for 24 h. (B) Effect of homologous β2-adrenoceptor desensitization on the in vitro responsiveness to 10 µmol·L−1 salbutamol (Sal) or 1 µmol·L−1 forskolin (Fsk). (C) Densitometric analyses of β2-adrenoceptor. (D) RT-PCR image of peroxisome-proliferator-activated receptor (PPAR)γ gene expression and (E) a representative electrophoretic mobility shift assay gel showing the binding specificity of PPARγ to the DNA probe and a bar graph illustrating the densitometric analyses of PPAR-binding activity. Results are average of five separate experiments. Data are reported as mean ± standard error of the mean (SEM). *P < 0.05; ***P < 0.001.