与年龄有关的高血压中的骨骼肌活性氧和微血管内皮功能:使用微透析技术的研究方案。

IF 4.7 2区 医学 Q1 NEUROSCIENCES Journal of Physiology-London Pub Date : 2024-11-09 DOI:10.1113/JP287187
Hollie Speer, Mostafa M Ali, Nathan M D'Cunha, Nenad Naumovski, Stephan F E Praet, Robert C Hickner, Andrew J McKune
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引用次数: 0

摘要

随着自然衰老,活性氧(ROS)生成增加,微血管内皮受损,但这往往发生在发现包括高血压在内的心脏代谢疾病之前。与年龄相关的血压升高是由复杂的系统变化驱动的,其综合机制尚不清楚。从中年开始,骨骼肌的衰老与微血管血流量减少和外周阻力增加有关,这表明肌肉中的血管舒张功能下降可能先于与年龄有关的血压升高。随着年龄的增长,血管和骨骼肌系统的结构和功能变化会影响氧化还原平衡,反之亦然,从而进一步加剧微血管内皮功能障碍。因此,对健康人群和高血压人群的微血管环境进行比较,可以深入了解在功能显著下降期间发生的变化。本综合研究方案介绍了一种微透析技术,用于评估微血管健康与肌肉功能变化之间的相互作用,目前还无法以其他方式解决这一问题。在此,我们详细介绍了一种实验方案,该方案可同时检测骨骼肌 ROS(H2O2 和间接 O2-)、确定营养血流量并评估微血管内皮功能对乙酰胆碱刺激的反应。我们预计,与高血压患者或老年人相比,健康的中年人在静息状态下肌肉中产生的 ROS 应该不会增加,但可能会表现出微血管功能紊乱。所述技术允许对微血管生理学进行复杂的探索,这将为确定与年龄有关的高血压潜在发展机制提供重要的新见解,并有助于早期识别和预防。要点在高血压等与年龄有关的心脏代谢和血管疾病发生之前,活性氧(ROS)生成增加和微血管内皮功能失调就已经存在。从中年开始,血管和骨骼肌的结构和功能发生了深刻变化,这促使人们需要从机理上探索健康人和高血压患者的微血管环境。利用一种新型微透析技术,我们详细介绍了同时检测骨骼肌 ROS(H2O2 和间接 O2-)、确定营养血流量和评估微血管内皮功能对乙酰胆碱刺激反应的实验方案。利用这种技术和研究方案,我们可以揭示静息状态下 ROS 生成和微血管内皮的潜在扰动的功能性见解,这些扰动在与年龄有关的高血压的发展中发挥着重要作用。
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Skeletal muscle reactive oxygen species and microvascular endothelial function in age-related hypertension: a study protocol using a microdialysis technique.

Increased reactive oxygen species (ROS) generation and microvascular endothelial disruptions occur with natural ageing, but often transpire before the detection of cardiometabolic conditions including hypertension. Age-related increases in blood pressure are driven by complex systemic changes with poorly understood integrated mechanisms. The deconditioning experienced by ageing skeletal muscle from mid-life is associated with reduced microvascular blood flow and increased peripheral resistance, suggesting that vasodilatory decrements in the muscle may precede the age-related increases in blood pressure. Structural and functional changes within the vascular and skeletal muscle systems with advancing age can influence redox homeostasis, and vice versa, further compounding microvascular endothelial dysfunction. Therefore, comparisons between the microvascular environments of healthy and hypertensive cohorts can provide insights into the changes that occur during significant periods of functional decline. This comprehensive study protocol describes a microdialysis technique to assess the interactions of microvascular health and functional changes in the muscle, which currently cannot be otherwise addressed. Here, we detail an experimental protocol to simultaneously detect skeletal muscle ROS (H2O2 and indirect O2 -), determine nutritive blood flow and assess microvascular endothelial function in response to acetylcholine stimulation. We expect that healthy middle-aged individuals should not have increased ROS generation in the muscle at rest, compared to their hypertensive or older counterparts, but may exhibit perturbed microvascular function. The described technique allows for intricate exploration of microvascular physiology that will provide a critically novel insight into benchmarking potential age-related mechanisms involved in the development of age-related hypertension, and aid in early identification and prevention. KEY POINTS: Increased reactive oxygen species (ROS) production and microvascular endothelial dysfunction precede the onset of age-related cardiometabolic and vascular conditions such as hypertension. The profound structural and functional changes that occur within the vasculature and in skeletal muscle from middle age prompt a need to mechanistically explore the microvascular environment in healthy and hypertensive individuals. Using a novel microdialysis technique, we detail an experimental protocol to simultaneously detect skeletal muscle ROS (H2O2 and indirect O2 -), determine nutritive blood flow and assess microvascular endothelial function in response to acetylcholine stimulation. With this technique and study protocol, we can reveal functional insights into potential perturbations in ROS generation at rest and the microvascular endothelium, which play important roles in the development of age-related hypertension.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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