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. 2019 Mar 18;12(3):e007071. doi: 10.1161/CIRCEP.118.007071

Figure 2.

Figure 2.

Valproic acid (VPA) treatment attenuates ultrastructural remodeling in CREM-IbΔC-X transgenic (TG) mice atria. Representative electron microscopic images of atrial tissue and quantitative analysis (area proportions in %) of sarcomeres, mitochondria, collagen fibers, lipofuscin granules, and glycogen in the indicated groups during (A) short-term (7th wk) and (B) long-term (16th wk) treatment. With age, myolysis dominated in TGVEH atrial cardiomyocytes and accumulation of collagen fibers between cells was enhanced. VPA attenuated this ultrastructural disarrangement after short- and long-term treatment in transgenic atria (TGVPA; n=3–4 animals/group; average of 16–18 pictures/animal; *P<0.05 vs wild-type (WT; all areas); †P<0.05 vs vehicle (VEH; other, collagen, sarcomeres), mitochondria: not significant). CREM-IbΔC-X indicates CREM (cAMP responsive element modulator) isoform IbΔC-X.