Sayegh Ana Luiza C, Plunkett Michael J, Babbage Thalia, Dawes Mathew, Paton Julian F R, Fisher James P
Department of Physiology, Manaaki Manawa - The Centre for Heart Research, Faculty of Medical & Health Sciences, University of Auckland, Auckland, New Zealand.
Department of Medicine, Faculty of Medical & Health Sciences, University of Auckland, Auckland, New Zealand.
J Physiol. 2025 Sep;603(18):5091-5102. doi: 10.1113/JP286998. Epub 2024 Sep 14.
We tested the hypothesis that in human hypertension, an increased tonicity/sensitivity of the peripheral chemoreflex causes a sympathetically mediated restraint of nutritive blood flow to the exercising muscles. Fourteen patients with treated hypertension (age 69 ± 11 years, 136 ± 12/80 ± 11 mmHg; mean ± SD) were studied under conditions of intravenous 0.9% saline (control) and low-dose dopamine (2 µg kg min) to inhibit the peripheral chemoreflex, at baseline, during isocapnic hypoxic rebreathing and during rhythmic handgrip exercise (3 min, 50% maximum voluntary contraction). At baseline, dopamine did not change mean blood pressure (95 ± 10 vs. 98 ± 10 mmHg, P = 0.155) but increased brachial artery blood flow (59 ± 20 vs. 48 ± 16 ml min, P = 0.030) and vascular conductance (0.565 ± 0.246 vs. 0.483 ± 0.160 ml min mmHg; P = 0.039). Dopamine attenuated the increase in mean blood pressure (∆3 ± 4 vs. ∆8 ± 6 mmHg, P = 0.007) to isocapnic hypoxic rebreathing and reduced peripheral chemoreflex sensitivity by 28 ± 37% (P = 0.044). Rhythmic handgrip exercise induced increases in brachial artery blood flow and vascular conductance (both P < 0.05 vs. rest after 45 s) that were greater with dopamine than saline (e.g. Δ76 ± 54 vs. Δ60 ± 43 ml min and Δ0.730 ± 0.440 vs. Δ0.570 ± 0.424 ml min mmHg, respectively, at 60 s; main effect of condition both P < 0.0001). Our results indicate that the peripheral chemoreflex is tonically active at rest and restrains the blood flow and vascular conductance increases to exercise in treated human hypertension. KEY POINTS: It was hypothesised that in human hypertension, an increased tonicity/sensitivity of the peripheral chemoreflex causes a sympathetically mediated restraint of nutritive blood flow to the exercising muscles. Treated patients with hypertension (n = 14) were studied under conditions of intravenous 0.9% saline (control) and low-dose dopamine (2 µg kg min) to inhibit the peripheral chemoreflex. Low-dose dopamine reduced resting ventilation and peripheral chemoreflex sensitivity, and while mean blood pressure was unchanged, brachial artery blood flow and vascular conductance were increased. Low-dose dopamine augmented the brachial artery blood flow and vascular conductance responses to rhythmic handgrip. These findings indicate that the peripheral chemoreflex is tonically active at rest and restrains the blood flow, and vascular conductance increases to exercise in treated human hypertension.
在人类高血压中,外周化学反射的张力/敏感性增加会导致交感神经介导的对运动肌肉营养性血流的限制。研究了14例接受治疗的高血压患者(年龄69±11岁,血压136±12/80±11 mmHg;均值±标准差),分别在静脉输注0.9%生理盐水(对照)和低剂量多巴胺(2 μg·kg·min)以抑制外周化学反射的情况下进行研究,研究条件包括基线状态、等碳酸性低氧再呼吸期间以及节律性握力运动(3分钟,最大自主收缩的50%)期间。在基线状态下,多巴胺未改变平均血压(95±10 vs. 98±10 mmHg,P = 0.155),但增加了肱动脉血流(59±20 vs. 48±16 ml/min,P = 0.030)和血管传导率(0.565±0.246 vs. 0.483±0.160 ml/min·mmHg;P = 0.039)。多巴胺减弱了等碳酸性低氧再呼吸引起的平均血压升高(∆3±4 vs. ∆8±6 mmHg,P = 0.007),并使外周化学反射敏感性降低了28±37%(P = 0.044)。节律性握力运动引起肱动脉血流和血管传导率增加(45秒后与静息状态相比,两者P均<0.05),多巴胺组增加幅度大于生理盐水组(例如,60秒时分别为Δ76±54 vs. Δ60±43 ml/min和Δ0.730±0.440 vs. Δ0.570±0.424 ml/min·mmHg;状态的主要效应两者P均<0.0001)。我们的结果表明,外周化学反射在静息时具有紧张性活动,并限制了接受治疗的高血压患者运动时的血流和血管传导率增加。要点:假设在人类高血压中,外周化学反射的张力/敏感性增加会导致交感神经介导的对运动肌肉营养性血流的限制。对14例接受治疗的高血压患者在静脉输注0.9%生理盐水(对照)和低剂量多巴胺(2 μg·kg·min)以抑制外周化学反射的情况下进行研究。低剂量多巴胺降低了静息通气和外周化学反射敏感性,虽然平均血压未改变,但肱动脉血流和血管传导率增加。低剂量多巴胺增强了肱动脉血流和血管传导率对节律性握力的反应。这些发现表明,外周化学反射在静息时具有紧张性活动,并限制了接受治疗的高血压患者运动时的血流和血管传导率增加。