首页> 美国卫生研究院文献>American Journal of Physiology - Heart and Circulatory Physiology >Vascular Biology and Microcirculation: Chronic atorvastatin and exercise can partially reverse established skeletal muscle microvasculopathy in metabolic syndrome
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Vascular Biology and Microcirculation: Chronic atorvastatin and exercise can partially reverse established skeletal muscle microvasculopathy in metabolic syndrome

机译:血管生物学和微循环:慢性阿托伐他汀和运动可以部分逆转代谢综合征中已建立的骨骼肌微血管病变

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摘要

It has long been known that chronic metabolic disease is associated with a parallel increase in the risk for developing peripheral vascular disease. Although more clinically relevant, our understanding about reversing established vasculopathy is limited compared with our understanding of the mechanisms and development of impaired vascular structure/function under these conditions. Using the 13-wk-old obese Zucker rat (OZR) model of metabolic syndrome, where microvascular dysfunction is sufficiently established to contribute to impaired skeletal muscle function, we imposed a 7-wk intervention of chronic atorvastatin treatment, chronic treadmill exercise, or both. By 20 wk of age, untreated OZRs manifested a diverse vasculopathy that was a central contributor to poor muscle performance, perfusion, and impaired O2 exchange. Atorvastatin or exercise, with the combination being most effective, improved skeletal muscle vascular metabolite profiles (i.e., nitric oxide, PGI2, and thromboxane A2 bioavailability), reactivity, and perfusion distribution at both individual bifurcations and within the entire microvascular network versus responses in untreated OZRs. However, improvements to microvascular structure (i.e., wall mechanics and microvascular density) were less robust. The combination of the above improvements to vascular function with interventions resulted in an improved muscle performance and O2 transport and exchange versus untreated OZRs, especially at moderate metabolic rates (3-Hz twitch contraction). These results suggest that specific interventions can improve specific indexes of function from established vasculopathy, but either this process was incomplete after 7-wk duration or measures of vascular structure are either resistant to reversal or require better-targeted interventions.>NEW & NOTEWORTHY We used atorvastatin and/or chronic exercise to reverse established microvasculopathy in skeletal muscle of rats with metabolic syndrome. With established vasculopathy, atorvastatin and exercise had moderate abilities to reverse dysfunction, and the combined application of both was more effective at restoring function. However, increased vascular wall stiffness and reduced microvessel density were more resistant to reversal.Listen to this article’s corresponding podcast at .
机译:早就知道,慢性代谢性疾病与发展为周围血管疾病的风险平行增加有关。尽管在临床上更相关,但与我们对在这些情况下受损的血管结构/功能的机制和发展的了解相比,我们对逆转已确立的血管病的理解是有限的。使用13周龄的肥胖Zucker大鼠(OZR)代谢综合征模型,其中微血管功能障碍已充分确立,可导致骨骼肌功能受损,我们对慢性阿托伐他汀治疗,慢性跑步机锻炼或两者同时实施了7周干预。到20周龄时,未经治疗的OZR表现出多种血管病变,是导致肌肉性能差,灌注和O2交换受损的重要原因。阿托伐他汀或运动,最有效的组合,可改善骨骼肌血管代谢物谱(即一氧化氮,PGI2和血栓烷A2的生物利用度),反应性和单个分叉处以及整个微血管网络内的灌注分布,而未经治疗OZR。但是,对微血管结构(即壁力学和微血管密度)的改进不够牢固。与未经治疗的OZR相比,上述对血管功能的改善与干预相结合可改善肌肉性能以及O2的运输和交换,尤其是在中等代谢率(3-Hz抽搐收缩)下。这些结果表明,特定的干预措施可以改善已确定的血管病变的特定功能指标,但是要么持续7周后该过程仍不完全,要么血管结构的测量结果难以逆转,或者需要针对性更强的干预措施。>新的和值得注意的我们使用阿托伐他汀和/或长期锻炼来逆转代谢综合征大鼠骨骼肌中已建立的微血管病变。随着血管病的发展,阿托伐他汀和运动具有中等的逆转功能,并且两者的联合应用在恢复功能上更有效。但是,增加血管壁刚度和降低微血管密度更能抵抗逆转。请参阅本文相应的播客,网址为。

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