Find in Library

This study aimed to provide a more comprehensive molecular insight into the effects of aerobic exercise (AE), protein intake (PI), and AE combined with PI on human skeletal muscle by comparing their transcriptomic profiles. Fourteen published datasets obtained from the Gene Expression Omnibus (GEO) database were used. The hub genes were identified in response to acute AE (<i>ACTB</i>, <i>IL6</i>), training AE (<i>UBB</i>, <i>COL1A1</i>), PI (<i>EZH2</i>), acute AE combined with PI (<i>DDIT3</i>), and training AE combined with PI (<i>MYC</i>). Both <i>FOS</i> and <i>MYC</i> were upregulated in response to acute AE, and they were, respectively, downregulated by higher PI and a combination of AE and PI. <i>COL1A1</i> was upregulated by training AE but was downregulated by higher PI. Results from the gene set enrichment analysis (<i>p</i> < 0.05 and FDR < 25%) showed that AE and PI delivered their impacts on human skeletal muscle in analogous pathways, including aerobic respiration, mitochondrial complexes, extracellular matrix (ECM) remodeling, metabolic process, and immune/inflammatory responses, whereas, PI may attenuate the response of immune/inflammation and ECM remodeling which would be promoted by AE, irrespective of its types. Compared to PI alone, acute AE combined with PI would further promote protein turnover and synthesis, but suppress skeletal muscle contraction and movement.