Postgraduate Program in Rehabilitation and Functional Performance, Ribeirão Preto Medical School, University of São Paulo (USP), Avenida Bandeirantes, 3900, Monte Alegre, Ribeirão Preto 14040-907, Brazil.
School of Physical Education and Sport of Ribeirão Preto, University of São Paulo (USP), Avenida Bandeirantes, 3900, Monte Alegre, Ribeirão Preto 14040-907, Brazil.
Int J Mol Sci. 2021 Mar 5;22(5):2635. doi: 10.3390/ijms22052635.
Although physical exercise-induced autophagy activation has been considered a therapeutic target to enhance tissue health and extend lifespan, the effects of different exercise models on autophagy in specific metabolic tissues are not completely understood. This descriptive investigation compared the acute effects of endurance (END), exhaustive (ET), strength (ST), and concurrent (CC) physical exercise protocols on markers of autophagy, genes, and proteins in the gastrocnemius muscle, heart, and liver of mice. The animals were euthanized immediately (0 h) and six hours (6 h) after the acute exercise for the measurement of glycogen levels, mRNA expression of , , , , , , , , and protein levels of Beclin 1 and ATG5. The markers of autophagy were measured by quantifying the protein levels of LC3II and Sqstm1/p62 in response to three consecutive days of intraperitoneal injections of colchicine. In summary, for gastrocnemius muscle samples, the main alterations in mRNA expressions were observed after 6 h and for the ST group, and the markers of autophagy for the CC group were increased (i.e., LC3II and Sqstm1/p62). In the heart, the Beclin 1 and ATG5 levels were downregulated for the ET group. Regarding the markers of autophagy, the Sqstm1/p62 in the heart tissue was upregulated for the END and ST groups, highlighting the beneficial effects of these exercise models. The liver protein levels of ATG5 were downregulated for the ET group. After the colchicine treatment, the liver protein levels of Sqstm1/p62 were decreased for the END and ET groups compared to the CT, ST, and CC groups. These results could be related to diabetes and obesity development or liver dysfunction improvement, demanding further investigations.
尽管运动诱导的自噬激活已被认为是增强组织健康和延长寿命的治疗靶点,但不同运动模式对特定代谢组织中自噬的影响尚不完全清楚。本研究采用描述性方法比较了耐力(END)、力竭(ET)、力量(ST)和并合(CC)急性运动方案对小鼠腓肠肌、心脏和肝脏中自噬标志物、基因和蛋白的影响。动物在急性运动后立即(0 h)和 6 小时(6 h)处死,用于测量糖原水平、 和 、 、 、 、 、 和 Beclin 1 和 ATG5 蛋白水平的 mRNA 表达。通过定量 LC3II 和 Sqstm1/p62 蛋白水平来检测自噬标志物,以响应连续三天的腹腔注射秋水仙素。总之,对于腓肠肌样本,主要的 mRNA 表达变化发生在 6 h 后和 ST 组,CC 组的自噬标志物增加(即 LC3II 和 Sqstm1/p62)。在心脏中,ET 组的 Beclin 1 和 ATG5 水平下调。关于自噬标志物,END 和 ST 组的心脏组织中 Sqstm1/p62 上调,突出了这些运动模型的有益作用。ET 组的肝组织 ATG5 蛋白水平下调。秋水仙素处理后,与 CT、ST 和 CC 组相比,END 和 ET 组的肝组织 Sqstm1/p62 蛋白水平下降。这些结果可能与糖尿病和肥胖症的发展或肝功能改善有关,需要进一步研究。