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. 2020 Jun 12;115(4):43. doi: 10.1007/s00395-020-0799-x

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — RBC from anaemic and eNOS deficient mice impair the recovery of LV function after ischemia/reperfusion. a Blood samples from anaemic WT mice and non-anaemic eNOS^−/− mice deteriorated in b left ventricular developed pressure (LVDP), c maximum rate of pressure increase (dP/dt_max) and d (dP/dt_min), as compared to sham mice (I). These effects were all specific for RBC (II). Control experiments revealed the cardioprotective effects of RBC from sham mice in recipient hearts after ischaemia/reperfusion (III). Data are mean ± SD from n = 7–11 (sham), n = 7–10 (anaemia), n = 6–8 (eNOS ^−/−) and n = 5 (buffer) mice/group