Division of Environmental Physiology, Swedish Aerospace Physiology Center, KTH Royal Institute of Technology, Stockholm, Sweden.
Am J Physiol Heart Circ Physiol. 2021 Apr 1;320(4):H1303-H1312. doi: 10.1152/ajpheart.00763.2020. Epub 2021 Jan 22.
The aims were to study effects of iterative exposures to moderate elevations of local intravascular pressure on arterial/arteriolar stiffness and plasma levels of vasoactive substances. Pressures in the vasculature of an arm were increased by 150 mmHg in healthy men ( = 11) before and after a 5-wk regimen, during which the vasculature in one arm was exposed to fifteen 40-min sessions of moderately increased transmural pressure (+65 to +105 mmHg). This vascular pressure training and the pressure-distension determinations were conducted by exposing the subjects' arm versus remaining part of the body to differential ambient pressure. During the pressure-distension determinations, venous samples were simultaneously obtained from pressurized and unpressurized vessels. Pressure training reduced arterial pressure distension by 40 ± 23% and pressure-induced flow by 33 ± 30% ( < 0.01), but only in the pressure-trained arm, suggesting local adaptive mechanisms. The distending pressure-diameter and distending pressure-flow curves, with training-induced increments in pressure thresholds and reductions in response gains, suggest that the increased precapillary stiffness was attributable to increased contractility and structural remodeling of the walls. Acute vascular pressure provocation induced local release of angiotensin-II (ANG II) and endothelin-1 (ET-1) ( < 0.05), suggesting that these vasoconstrictors limited the pressure distension. Pressure training increased basal levels of ET-1 and induced local pressure release of matrix metalloproteinase 7 ( < 0.05), suggesting involvement of these substances in vascular remodeling. The findings are compatible with the notion that local intravascular pressure load acts as a prime mover in the development of primary hypertension. Adaptive responses to arterial/arteriolar pressure elevation have typically been investigated in cross-sectional studies in hypertensive patients or in longitudinal studies in experimental animals. The present investigation shows that in healthy individuals, fifteen 40-min, carefully controlled, moderate transmural pressure elevations markedly increase in vivo stiffness (i.e. reduce pressure distension) in arteries and arterioles. The response is mediated via local mechanisms, and it appears that endothelin-1, angiotensin-II, and matrix metalloproteinase 7 may have key roles.
目的是研究反复暴露于局部血管内压力适度升高对动脉/小动脉僵硬和血管活性物质血浆水平的影响。在 11 名健康男性中,通过将手臂血管内的压力增加 150mmHg 来增加血管内压力(= 11),然后在 5 周的治疗方案中,通过将手臂血管暴露于 15 次 40 分钟的中度增加的跨壁压力(+65 至+105mmHg)来增加血管内压力。这种血管压力训练和压力扩张测定是通过使受试者的手臂与身体的其余部分暴露于差异环境压力来进行的。在压力扩张测定期间,同时从加压和未加压的血管中获得静脉样本。压力训练使动脉压力扩张减少了 40±23%,压力诱导的流量减少了 33±30%(<0.01),但仅在接受压力训练的手臂中,这表明存在局部适应性机制。随着压力阈值的增加和响应增益的降低,扩张压力-直径和扩张压力-流量曲线表明,前毛细血管僵硬度的增加归因于壁的收缩性和结构重塑的增加。急性血管压力激发诱导局部释放血管紧张素-II(ANG II)和内皮素-1(ET-1)(<0.05),这表明这些血管收缩剂限制了压力扩张。压力训练增加了 ET-1 的基础水平,并诱导了基质金属蛋白酶 7 的局部压力释放(<0.05),这表明这些物质参与了血管重塑。这些发现与局部血管内压力负荷作为原发性高血压发展的主要动力的观点是一致的。对动脉/小动脉压力升高的适应性反应通常在高血压患者的横断面研究或实验动物的纵向研究中进行研究。本研究表明,在健康个体中,15 次 40 分钟的、精心控制的、适度的跨壁压力升高可显著增加动脉和小动脉的体内僵硬度(即减少压力扩张)。这种反应是通过局部机制介导的,并且似乎内皮素-1、血管紧张素-II 和基质金属蛋白酶 7 可能具有关键作用。