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. 2020 Mar 17;25:3. doi: 10.1186/s40001-020-00404-7

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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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — miR-34a improves ACE and ACE2 by inhibiting the expression of PAI-1 by Western Blot. a ACE and ACE2 protein expression detection by WB. b Quantitative results. *P < 0.05, compared with normal group; ^#P < 0.05, compared with model group; ^&P < 0.05, compared with NC group; ^$P < 0.05, compared with miR-34a mimic group; ^@P < 0.05, compared with miR-34a inhibitor group; ^△P < 0.05, compared with Si-PAI-1 group. NC negative control, ACE angiotensin-converting enzyme (ACE)