JSC "Sites-Tsentr", 123182 Moscow, Russia.
Department of Computational Biology, Scientific Center for Information Technologies and Artificial Intelligence, Sirius University of Science and Technology, 354340 Sochi, Russia.
Int J Mol Sci. 2023 Jul 7;24(13):11223. doi: 10.3390/ijms241311223.
Optimizing physical training regimens to increase muscle aerobic capacity requires an understanding of the internal processes that occur during exercise that initiate subsequent adaptation. During exercise, muscle cells undergo a series of metabolic events that trigger downstream signaling pathways and induce the expression of many genes in working muscle fibers. There are a number of studies that show the dependence of changes in the activity of AMP-activated protein kinase (AMPK), one of the mediators of cellular signaling pathways, on the duration and intensity of single exercises. The activity of various AMPK isoforms can change in different directions, increasing for some isoforms and decreasing for others, depending on the intensity and duration of the load. This review summarizes research data on changes in the activity of AMPK, Ca/calmodulin-dependent protein kinase II (CaMKII), and other components of the signaling pathways in skeletal muscles during exercise. Based on these data, we hypothesize that the observed changes in AMPK activity may be largely related to metabolic and signaling transients rather than exercise intensity per se. Probably, the main events associated with these transients occur at the beginning of the exercise in a time window of about 1-10 min. We hypothesize that these transients may be partly due to putative trigger-like kinase/protein phosphatase interactions regulated by feedback loops. In addition, numerous dynamically changing factors, such as [Ca], metabolite concentration, and reactive oxygen and nitrogen species (RONS), can shift the switching thresholds and change the states of these triggers, thereby affecting the activity of kinases (in particular, AMPK and CaMKII) and phosphatases. The review considers the putative molecular mechanisms underlying trigger-like interactions. The proposed hypothesis allows for a reinterpretation of the experimental data available in the literature as well as the generation of ideas to optimize future training regimens.
优化体能训练方案以提高肌肉有氧能力,需要了解运动过程中引发后续适应的内部过程。运动时,肌肉细胞经历一系列代谢事件,触发下游信号通路,并诱导工作肌纤维中许多基因的表达。有许多研究表明,细胞信号通路中介物之一 AMP 激活蛋白激酶(AMPK)的活性变化取决于单次运动的持续时间和强度。不同 AMPK 同工型的活性可以朝着不同的方向变化,一些同工型的活性增加,而另一些同工型的活性降低,具体取决于负荷的强度和持续时间。本综述总结了运动过程中骨骼肌中 AMPK、Ca/钙调蛋白依赖性蛋白激酶 II(CaMKII)和其他信号通路成分活性变化的研究数据。基于这些数据,我们假设观察到的 AMPK 活性变化可能主要与代谢和信号瞬变有关,而不是运动强度本身。可能,与这些瞬变相关的主要事件发生在运动开始时,时间窗口约为 1-10 分钟。我们假设这些瞬变可能部分归因于受反馈回路调节的假定触发样激酶/蛋白磷酸酶相互作用。此外,许多动态变化的因素,如 [Ca]、代谢物浓度、活性氧和氮物种(RONS),可以改变这些触发的切换阈值并改变它们的状态,从而影响激酶(特别是 AMPK 和 CaMKII)和磷酸酶的活性。综述考虑了假定的触发样相互作用的分子机制。提出的假设允许重新解释现有文献中的实验数据,并产生优化未来训练方案的思路。