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. Author manuscript; available in PMC: 2011 May 11.

Published in final edited form as: Circ Res. 2008 Mar 20;102(9):1127–1136. doi: 10.1161/CIRCRESAHA.107.163642

Cardiac myocytes were isolated from control (A) or 4W-MR (B) LV as described in materials and methods. (A, B) representative immunoblots showing accumulation of phospho-FAK, -p38-MAPK, -Hsp27, and -AKT after treatment with 10µmol/L isoproterenol (Iso) or 1µmol/L Zinterol (Zint) for 5-minutes compared with control (Ctrl): 1µmol/L of CGP20712A was added 30-minutes before isoproterenol stimulation. (C) Summary graphs represent quantitative data from 4 independent experiments from cells derived from 4 different animals. *P<0.05 vs. control.

Cardiac myocytes were isolated from control (A) or 4W-MR (B) LV as described in materials and methods. (A, B) representative immunoblots showing accumulation of phospho-FAK, -p38-MAPK, -Hsp27, and -AKT after treatment with 10µmol/L isoproterenol (Iso) or 1µmol/L Zinterol (Zint) for 5-minutes compared with control (Ctrl): 1µmol/L of CGP20712A was added 30-minutes before isoproterenol stimulation. (C) Summary graphs represent quantitative data from 4 independent experiments from cells derived from 4 different animals. *P<0.05 vs. control.