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. 2011 Mar 14;108(13):5331–5336. doi: 10.1073/pnas.1102116108

Fig. 4.

Fig. 4.

Analysis of skeletal muscle of dystrophin-null fish that survive 30 d after treatment with chemical 4, aminophylline. (A) H&E staining of WT, nontreated, and chemical 4-treated fish. Nontreated dystrophin-null fish have disorganized structure (arrow) in skeletal muscle. The dystrophin-null fish with treated aminophylline have normal structure in skeletal muscle. (B) Immunostaining of WT, nontreated, and chemical 4-treated fish with anti-myosin heavy chain and anti-laminin antibody. Nontreated dystrophin-null fish have broken and disturbed structure (arrows) of skeletal muscle fibers. The treated dystrophin-null fish with aminophylline have normal structure in skeletal muscle. (C) Immunoblot of phosphorylated PKA and PKA at 30 dpf in surviving fish. WT, wild type; NT, nontreatment of dystrophin-null fish; CT, chemical 4-treated dystrophin-null fish. (D) Ratio of phosphorylated PKA and PKA in 30 dpf surviving fish (n = 3). Blue, WT; light blue, nontreatment of dystrophin-null fish; red, chemical 4-treated dystrophin-null fish. *P < 0.05 (vs. WT and nontreatment groups). Error bars indicate SDs. (E) Assay of cAMP-dependent PK activity (n = 3). Bars show the ratio of phosphorylated peptides and nonphosphorylated peptide. Blue, WT fish treated with chemical 4 (2.5 μg/mL) for 30 d. Red, affected sapje fish treated with chemical 4 (2.5 μg/mL). Light blue, nontreated WT fish. Yellow, nontreated affected sapje fish. *P < 0.05 (vs. nontreated WT and mutant fish). Error bars indicate SDs.