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. 2021 Mar 17;12(4):283. doi: 10.1038/s41419-021-03577-z

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© The Author(s) 2021

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. 5 — Confluent PCT cells were treated or not with 30 µM GC7 for 24 h and then used for different analysis. a At the end of treatment cells were deprived in glucose and the efflux of glucose was measured in the next 8 h. Dots displayed mean ± SD of three independent experiments. b Western blot analysis of GLUT1 and GLUT2 expressions in membrane enriched protein lysate from PCT cells. β-Actin was used as loading control. MW molecular weight. *p < 0.05 evaluated using Mann–Whitney test.