Cardiorespiratory fitness as a key predictor of metabolic, inflammatory, and oxidative stress biomarkers in adults with different physical activity levels

IF 8.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Omar A. Hernández-López , Blanca Murillo-Ortíz , Clara Luna-Marco , Julia Cacace , Alberto Hermo-Argibay , Victoria Ramírez , Martha Guevara-Cruz , María Pelechá-Salvador , Milagros Rocha , Susana Rovira-Llopis , Víctor M. Víctor , Iván Torre-Villalvazo
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Abstract

Sedentary lifestyles are associated with poor cardiorespiratory fitness (CRF) and predispose individuals to cardiometabolic diseases and increased all-cause mortality, events related to oxidative stress and inflammation. While regular exercise induces adaptations that improve metabolic homeostasis, its antioxidant effects are not fully characterised. This cross-sectional study compared antioxidant gene/protein expression in peripheral blood mononuclear cells (PBMCs) and metabolic, inflammatory, and oxidative stress biomarkers in sedentary and active individuals, and analysed potential associations with CRF.
Fifty-one healthy adults (18–45 years) were recruited. Participants were classified as sedentary (SED), physically active (PA), or endurance athletes (EA) using the International Physical Activity Questionnaire (IPAQ; n = 17/group). Anthropometric, biochemical, metabolic, and inflammatory variables were assessed. Oxidative stress was measured via serum hydrogen peroxide (H2O2) and malondialdehyde (MDA). PBMC protein/mRNA expression of nuclear factor erythroid 2-related factor 2 (NRF2) and antioxidant enzymes [superoxide dismutase 1 (SOD1), glutathione reductase (GSR), glutathione peroxidase 1 (GPX1), catalase (CAT)] were evaluated. Metabolic flexibility was assessed at rest by indirect calorimetry, and CRF by maximal oxygen uptake (VO2max mL·kg−1·min−1) during a progressive maximal cardiopulmonary exercise test.
The PA and EA groups showed greater metabolic flexibility and CRF than the SED group, which exhibited altered homeostasis model assessment of insulin resistance (HOMA-IR), triglyceride-to-high-density lipoprotein cholesterol ratio (TG/HDL-C), elevated tumour necrosis factor alpha (TNFα), high-sensitivity C-reactive protein (hsCRP), oxidative stress (H2O2, MDA), and reduced antioxidant gene/protein expression. Higher VO2max mL·kg−1·min−1 correlated with healthier metabolic profiles, less inflammation, and higher antioxidant expression, while inversely correlating with HOMA-IR, MDA, and TNFα.
Optimal or high CRF strongly protects against insulin resistance, oxidative stress, inflammation, and metabolic inflexibility, key hallmarks of sedentary behaviour. Regular physical exercise improves metabolic and redox profiles, enhancing antioxidant defences in PBMCs. A functional CRF threshold represents a practical target by which to reduce cardiometabolic risk.

Abstract Image

心肺健康是不同身体活动水平成人代谢、炎症和氧化应激生物标志物的关键预测因子
久坐不动的生活方式与较差的心肺功能(CRF)有关,使个体易患心脏代谢疾病,增加全因死亡率,以及与氧化应激和炎症相关的事件。虽然有规律的运动可以诱导适应,改善代谢稳态,但其抗氧化作用尚未完全确定。这项横断面研究比较了久坐和活跃个体外周血单个核细胞(PBMCs)和代谢、炎症和氧化应激生物标志物中的抗氧化基因/蛋白表达,并分析了与CRF的潜在关联。51名健康成人(18-45岁)被招募。使用国际体育活动问卷(IPAQ, n = 17/组)将参与者分为久坐(SED)、体力活动(PA)或耐力运动员(EA)。评估人体测量学、生化、代谢和炎症变量。通过血清过氧化氢(H2O2)和丙二醛(MDA)测定氧化应激。检测PBMC蛋白/mRNA表达量,核因子-红细胞2相关因子2 (NRF2)和抗氧化酶[超氧化物歧化酶1 (SOD1)、谷胱甘肽还原酶(GSR)、谷胱甘肽过氧化物酶1 (GPX1)、过氧化氢酶(CAT)]的表达。在进行性最大心肺运动试验中,通过间接量热法评估静息时的代谢柔韧性,通过最大摄氧量(VO2max mL·kg-1·min-1)评估CRF。PA和EA组比SED组表现出更大的代谢灵活性和CRF,表现出胰岛素抵抗(HOMA-IR),甘油三酯与高密度脂蛋白胆固醇比率(TG/HDL-C),肿瘤坏死因子α (TNFα)升高,高敏c -反应蛋白(hsCRP),氧化应激(H2O2, MDA)和抗氧化基因/蛋白表达降低的稳态模型评估。较高的VO2max与更健康的代谢谱、更少的炎症和更高的抗氧化表达相关,而与HOMA-IR、MDA和tnf - α呈负相关。最佳或高CRF可以有效防止胰岛素抵抗、氧化应激、炎症和代谢不灵活性,这些都是久坐行为的关键特征。有规律的体育锻炼可以改善代谢和氧化还原谱,增强pbmc的抗氧化防御能力。功能性CRF阈值是降低心脏代谢风险的实际目标。
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来源期刊
Free Radical Biology and Medicine
Free Radical Biology and Medicine 医学-内分泌学与代谢
CiteScore
14.00
自引率
4.10%
发文量
850
审稿时长
22 days
期刊介绍: Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.
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