Wagenmakers Anton J M, Strauss Juliette A, Shepherd Sam O, Keske Michelle A, Cocks Matthew
Research Institute for Sport and Exercise Sciences, Liverpool John Moores University, Liverpool, L3 3AF, UK.
Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
J Physiol. 2016 Apr 15;594(8):2207-22. doi: 10.1113/jphysiol.2014.284513. Epub 2015 Feb 24.
This review concludes that a sedentary lifestyle, obesity and ageing impair the vasodilator response of the muscle microvasculature to insulin, exercise and VEGF-A and reduce microvascular density. Both impairments contribute to the development of insulin resistance, obesity and chronic age-related diseases. A physically active lifestyle keeps both the vasodilator response and microvascular density high. Intravital microscopy has shown that microvascular units (MVUs) are the smallest functional elements to adjust blood flow in response to physiological signals and metabolic demands on muscle fibres. The luminal diameter of a common terminal arteriole (TA) controls blood flow through up to 20 capillaries belonging to a single MVU. Increases in plasma insulin and exercise/muscle contraction lead to recruitment of additional MVUs. Insulin also increases arteriolar vasomotion. Both mechanisms increase the endothelial surface area and therefore transendothelial transport of glucose, fatty acids (FAs) and insulin by specific transporters, present in high concentrations in the capillary endothelium. Future studies should quantify transporter concentration differences between healthy and at risk populations as they may limit nutrient supply and oxidation in muscle and impair glucose and lipid homeostasis. An important recent discovery is that VEGF-B produced by skeletal muscle controls the expression of FA transporter proteins in the capillary endothelium and thus links endothelial FA uptake to the oxidative capacity of skeletal muscle, potentially preventing lipotoxic FA accumulation, the dominant cause of insulin resistance in muscle fibres.
本综述得出结论,久坐不动的生活方式、肥胖和衰老会损害肌肉微血管对胰岛素、运动和血管内皮生长因子A(VEGF-A)的血管舒张反应,并降低微血管密度。这两种损害都有助于胰岛素抵抗、肥胖和与年龄相关的慢性疾病的发展。积极的生活方式能使血管舒张反应和微血管密度保持在较高水平。活体显微镜检查表明,微血管单位(MVUs)是根据生理信号和肌肉纤维的代谢需求来调节血流的最小功能元件。一条普通终末小动脉(TA)的管腔直径控制着多达20条属于单个MVU的毛细血管的血流。血浆胰岛素增加以及运动/肌肉收缩会导致更多MVUs被调动起来。胰岛素还会增加小动脉的血管运动。这两种机制都会增加内皮表面积,从而通过存在于毛细血管内皮中高浓度的特定转运蛋白促进葡萄糖、脂肪酸(FAs)和胰岛素的跨内皮运输。未来的研究应该量化健康人群和高危人群之间转运蛋白浓度的差异,因为它们可能会限制肌肉中的营养物质供应和氧化,并损害葡萄糖和脂质的稳态。最近一项重要发现是,骨骼肌产生的VEGF-B控制着毛细血管内皮中脂肪酸转运蛋白的表达,从而将内皮脂肪酸摄取与骨骼肌的氧化能力联系起来,有可能防止脂毒性脂肪酸的积累,脂毒性脂肪酸积累是肌肉纤维中胰岛素抵抗的主要原因。