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. 2018 Sep 19;13(9):e0201401. doi: 10.1371/journal.pone.0201401

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© 2018 Kjeld et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 3 — (A) Specific content of OXPHOS CI (NDUFB8 = NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8) divers 1.0 ± 0.1 vs controls 1.0 ± 0.1, CII (SDHB = Succinate dehydrogenase [ubiquinone] iron-sulfur subunit) divers 1.0 ± 0.1 vs controls 1.0 ± 0.1, CIII (UQCRC2 = ubiquinol-cytochrome c reductase complex) divers 0.9 ± 0.1 vs controls 1.0 ± 0.1, CIV (MTCOI = mitochondrial cytochrome oxidase I) divers 0.9 ± 0.1 vs controls 1.0 ± 0.2, CV (ATP5A = ATP synthase subunit alpha) divers 0.9 ± 0.1 vs controls 1.0 ± 0.1. (B) Specific content of myoglobin divers 1.00 ± 0.03 vs. controls 1.00 ± 0.03. (C) SDS-page and western blot for determination of myoglobin. (D) Maximal CS (citrate synthase) activity divers 103.9 ± 10.0 vs. controls 98,0 ± 8.4 and HAD (3-hydroxyacyl CoA dehydrogenase) activity divers 10.0 ± 2.0 vs. controls 8.8 ± 2.0.