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. 2019 Mar 11;40(9):1168–1183. doi: 10.1038/s41401-018-0197-1

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — Effect of cyclosporine A (CSA) on the outcome of prolonged myocardial I/R. a Scheme of the experimental design. b CSA concentration in mouse serum during treatment (n = 6). c Comparison of echocardiographic parameters (LVEF, LVFS, LVESV, and LVEDV) between the VEH and CSA groups on the 7th and 14th days after MI (n = 11). d Representative images of Masson’s trichrome staining and average scar areas on post-MI day 28 (n = 11). VEH vehicle (control group), CSA cyclosporine A (treatment group). Data are shown as the mean ± SE; *P < 0.05 as indicated