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Figure 2


Fig. 2. Phosphorylation of p38-MAPK and Hsp-27 by CuCl2. (A,C) Protein (A, 50 µg or C, 100 µg) from Rana ridibunda hearts perfused in the absence (Con) or presence of increasing concentrations of CuCl2 (50–500 µmol l–1) for 15 min was analysed by immunoblotting with anti-p38-MAPK (Ai) and anti-Hsp27 (C) phosphospecific antibodies. As a positive control, extracts from hearts perfused with 50 µmol l–1 H2O2 for 2 min were included. Identical samples were assayed with an anti-actin antibody as a control for protein loading (Aii). (B,D) Densitometric analysis of phospho-p38-MAPK (B) and phospho-Hsp27 (D) bands, by laser scanning. Results are means ± s.e.m. for three independent experiments. *P<0.05, **P<0.01, {dagger}P<0.001 vs control value.





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