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与运动中最大脂肪氧化相关的生物标志物和遗传多态性:对代谢健康和运动表现的影响。

Biomarkers and genetic polymorphisms associated with maximal fat oxidation during physical exercise: implications for metabolic health and sports performance.

机构信息

Department of Chemical Sciences, Biomedical Sciences Institute, Ciudad Juarez Autonomous University, 32310, Chihuahua, Mexico.

Faculty of Physical Culture Sciences, Autonomous University of Chihuahua, 31000, Chihuahua, Mexico.

出版信息

Eur J Appl Physiol. 2022 Aug;122(8):1773-1795. doi: 10.1007/s00421-022-04936-0. Epub 2022 Apr 1.

DOI:10.1007/s00421-022-04936-0
PMID:35362801
Abstract

The maximal fat oxidation rate (MFO) assessed during a graded exercise test is a remarkable physiological indicator associated with metabolic flexibility, body weight loss and endurance performance. The present review considers existing biomarkers related to MFO, highlighting the validity of maximal oxygen uptake and free fatty acid availability for predicting MFO in athletes and healthy individuals. Moreover, we emphasize the role of different key enzymes and structural proteins that regulate adipose tissue lipolysis (i.e., triacylglycerol lipase, hormone sensitive lipase, perilipin 1), fatty acid trafficking (i.e., fatty acid translocase cluster of differentiation 36) and skeletal muscle oxidative capacity (i.e., citrate synthase and mitochondrial respiratory chain complexes II-V) on MFO variation. Likewise, we discuss the association of MFO with different polymorphism on the ACE, ADRB3, AR and CD36 genes, identifying prospective studies that will help to elucidate the mechanisms behind such associations. In addition, we highlight existing evidence that contradict the paradigm of a higher MFO in women due to ovarian hormones activity and highlight current gaps regarding endocrine function and MFO relationship.

摘要

在递增负荷运动试验中评估的最大脂肪氧化率(MFO)是一个显著的生理指标,与代谢灵活性、体重减轻和耐力表现有关。本综述考虑了与 MFO 相关的现有生物标志物,强调了最大摄氧量和游离脂肪酸可用性在预测运动员和健康个体 MFO 中的有效性。此外,我们强调了调节脂肪组织脂肪分解(即甘油三酯脂肪酶、激素敏感脂肪酶、脂联素 1)、脂肪酸转运(即脂肪酸易位酶簇分化 36)和骨骼肌氧化能力(即柠檬酸合酶和线粒体呼吸链复合物 II-V)的不同关键酶和结构蛋白在 MFO 变化中的作用。同样,我们讨论了 MFO 与 ACE、ADRB3、AR 和 CD36 基因不同多态性的关联,确定了有助于阐明这些关联背后机制的前瞻性研究。此外,我们强调了现有的证据,这些证据反驳了由于卵巢激素活性导致女性 MFO 更高的观点,并强调了关于内分泌功能和 MFO 关系的当前差距。

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