Effect of hypoxia-inducible factor 1 on vascular endothelial growth factor expression in exercised human skeletal muscle: a systematic review and meta-analysis
Date
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
American Physical Society
Abstract
Within contracting human skeletal muscle (SKM), oxygen pressure significantly drops, which has been linked to the activation of a signaling cascade mediated by hypoxia-inducible factor 1α (HIF-1α). This cascade leads to SKM angiogenesis through vascular endothelial growth factor (VEGF). However, the role of HIF-1α in exercise-induced VEGF expression within SKM remains unclear. In this study, we systematically reviewed the literature to quantitatively synthesize all available evidence on HIF-1α activation in exercised human muscle. We identified 21 studies providing 39 effect sizes of pre- and postexercise SKM HIF-1α data from 235 subjects, with 15 of them also presenting data on VEGF mRNA levels. HIF-1α mRNA increased in response to high-intensity and resistance exercise, regardless of participants' physical fitness levels. Notably, meta-regression showed that exercise-induced VEGF expression is not modulated by HIF-1α mRNA levels. Similarly, when plotting exercise-induced fold changes of VEGF and HIF-1α, no significant relationship was observed. Our findings demonstrate that HIF-1α is expressed in contracting SKM. However, the role of HIF-1α in the exercise-induced angiogenic response remains unclear, as most of the available evidence is limited to transcriptional data.<b>NEW & NOTEWORTHY</b> This analysis shows that both HIF-1α mRNA and protein levels are significantly elevated in skeletal muscle following dynamic exercise. However, the absence of a clear relationship between HIF-1α mRNA and the mRNA levels of its downstream target VEGF suggests that HIF-1α mRNA expression alone may not reliably reflect its regulatory role in VEGF transcription in response to exercise. Given the limited number of human studies examining posttranslational regulation of HIF-1α, its precise contribution to VEGF-mediated angiogenic signaling in exercised skeletal muscle remains uncertain.
Description
Citaciones: 7