College of Integrative Sciences and Arts, Arizona State University, Tempe, AZ, USA.
Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
J Diet Suppl. 2023;20(4):563-581. doi: 10.1080/19390211.2022.2039340. Epub 2022 Mar 1.
Mitochondrial biogenesis and destruction in skeletal muscle are coordinated by distinct signaling pathways that are influenced by internal and exogenous variables including, but not limited to, muscle phenotype, physical activity, dietary composition, or drug administration. Previously we found that long-term resveratrol administration (up to 480 mg/day) ameliorates the slow-to-fast phenotypic shift in soleus muscles and promotes the expression in slow myosin heavy chain in the mixed plantaris muscle of non-human primates consuming a high fat/sugar (HFS) diet. Here, we expand on these earlier findings by examining whether mitochondrial content and the markers that dictate their biogenesis and mitophagy/autophagy are similarly affected by HFS and/or influenced by resveratrol while consuming this diet (HFSR). Compared to controls ( = 9), there was ∼20-25% decrease in mitochondrial content in HFS ( = 8) muscles as reflected in the ratios using PCR analysis, which was blunted by resveratrol in HFSR ( = 7) soleus and, to a lesser degree, in plantaris muscles. ∼1.5 and 3-fold increase in Rev-erb-α protein was detected in HFSR soleus and plantaris muscles compared to controls, respectively. Unlike in HFSR animals, HFS soleus and plantaris muscles exhibited ∼2-fold elevation in phosphor-AMPKα (Thr172). HFS soleus muscles had elevated phosphorylated-to-total TANK binding protein-1 (TBK1) ratio suggesting an enhancement in mito/autophagic events. Taken together, resveratrol appears to blunt mitochondrial losses with a high fat/sugar diet by tempering mito/autophagy rather than promoting mitochondrial biogenesis, suggesting that the quantity of daily resveratrol supplement ingested and/or its long-term consumption are important considerations.Supplemental data for this article is available online at http://dx.doi.org/ .
线粒体生物发生和破坏在骨骼肌中是由不同的信号通路协调的,这些信号通路受内部和外部变量的影响,包括但不限于肌肉表型、身体活动、饮食组成或药物管理。之前我们发现,长期白藜芦醇给药(高达 480mg/天)可改善消耗高脂肪/糖(HFS)饮食的非人类灵长类动物比目鱼肌的慢肌向快肌表型转变,并促进混合比目鱼肌中慢肌球蛋白重链的表达。在这里,我们通过检查线粒体含量以及决定其生物发生和线粒体自噬/自噬的标志物是否同样受到 HFS 的影响,以及在消耗这种饮食(HFSR)时是否受到白藜芦醇的影响,来扩展这些早期发现。与对照组(n=9)相比,HFS(n=8)肌肉中线粒体含量下降了约 20-25%,这反映在 PCR 分析中的 比值上,而在 HFSR(n=7)比目鱼肌和在较小程度上在比目鱼肌中,白藜芦醇使这种下降趋势减弱。与对照组相比,HFSR 比目鱼肌和比目鱼肌中的 Rev-erb-α 蛋白分别增加了约 1.5 倍和 3 倍。与 HFSR 动物不同,HFS 比目鱼肌和比目鱼肌的磷酸化-AMPKα(Thr172)升高了约 2 倍。HFS 比目鱼肌中磷酸化到总 TANK 结合蛋白-1(TBK1)的比值升高,提示线粒体/自噬事件增强。总之,白藜芦醇似乎通过缓和线粒体自噬/自噬而不是促进线粒体生物发生来阻止高脂肪/糖饮食引起的线粒体丢失,这表明每天摄入的白藜芦醇补充剂的数量和/或其长期消耗是重要的考虑因素。本文的补充数据可在 http://dx.doi.org/ 在线获取。