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Inefficient functional sympatholysis is an overlooked cause of malperfusion in contracting skeletal muscle

机译:无效的功能性交感神经是骨骼肌收缩不足的原因

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摘要

Contracting skeletal muscle can overcome sympathetic vasoconstrictor activity (functional sympatholysis), which allows for a blood supply that matches the metabolic demand. This ability is thought to be mediated by locally released substances that modulate the effect of noradrenaline (NA) on the α-receptor. Tyramine induces local NA release and can be used in humans to investigate the underlying mechanisms and physiological importance of functional sympatholysis in the muscles of healthy and diseased individuals as well as the impact of the active muscles’ training status. In sedentary elderly men, functional sympatholysis and muscle blood flow are impaired compared to young men, but regular physical activity can prevent these age related impairments. In young subjects, two weeks of leg immobilization causes a reduced ability for functional sympatholysis, whereas the trained leg maintained this function. Patients with essential hypertension have impaired functional sympatholysis in the forearm, and reduced exercise hyperaemia in the leg, but this can be normalized by aerobic exercise training. The effect of physical activity on the local mechanisms that modulate sympathetic vasoconstriction is clear, but it remains uncertain which locally released substance(s) block the effect of NA and how this is accomplished. NO and ATP have been proposed as important inhibitors of NA mediated vasoconstriction and presently an inhibitory effect of ATP on NA signalling via P2 receptors appears most likely.
机译:收缩骨骼肌可以克服交感性血管收缩药的活动(功能性交感神经),使血液供应与代谢需求相匹配。认为该能力由调节去甲肾上腺素(NA)对α受体作用的局部释放物质介导。酪胺可诱导局部NA释放,可用于人类研究健康和患病个体肌肉中功能性交感神经的潜在机制和生理重要性,以及活跃肌肉的训练状态的影响。与年轻男子相比,久坐的久坐男性的功能性交感神经和肌肉血流受损,但定期进行体育锻炼可以预防这些与年龄有关的损害。在年轻受试者中,腿部固定两周会导致功能性交感神经功能降低,而受过训练的腿部则保持这种功能。患有原发性高血压的患者前臂的功能性交感神经受损,腿部运动性充血减少,但这可以通过有氧运动训练来恢复。体力活动对调节交感性血管收缩的局部机制的影响是显而易见的,但仍不确定哪种局部释放的物质会阻断NA的作用以及如何实现这种作用。已经提出了NO和ATP作为NA介导的血管收缩的重要抑制剂,目前ATP最有可能通过P2受体抑制NA信号传导。

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