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. 2019 Jan 30;19(4):2581–2590. doi: 10.3892/mmr.2019.9908

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Copyright: © Qin et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — RP increases the cell viability of MI/R-induced cardiomyocytes. (A) CCK-8 assay was performed on the cell viability of cardiomyocytes treated with different concentrations of RP. (B) CCK-8 assay was conducted to test the cell viability of cardiomyocytes treated with MI/R, 20 µM RP+MI/R, 40 µM RP+MI/R and 80 µM RP+MI/R, respectively. *P<0.05 vs. Control. RP, rhynchophylline; MI/R, myocardial ischemia-reperfusion; CCK-8, Cell Counting Kit-8.