心力衰竭伴射血分数降低的循环运动中交感神经兴奋的机制。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Catherine F Notarius, Mark B Badrov, Tomoyuki Tobushi, Daniel A Keir, Evan Keys, Dilafruz Hasanova, Paul Oh, John S Floras
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引用次数: 0

摘要

健康(HC)个体在轻度动态运动中腿部肌肉交感神经活动(MSNA)减少,但在年龄匹配的因射血分数(HFrEF)降低的心力衰竭患者中则没有。为了阐明这种交感神经兴奋的神经机制,我们研究了20例稳定的HFrEF患者(6F;平均年龄62±8 SD年),年龄匹配的HC 15例(6F;平均年龄59±7岁。在三种干预措施中,我们分别量化了静息时和单腿骑行期间(每次2分钟,轻度(无负荷)和中等强度(负荷= 30-40%)时的腓骨肌微神经图(微神经图):(1)运动后循环阻塞(PECO),它隔离了腿部肌肉代谢反射(MMR);(2)仰卧位,刺激心肺压力感受器(CPB);(3) 32%吸氧,抑制外周化学反射(PC)。单腿循环增加了HFrEF患者的MSNA并激活了腿部MMR,但HC患者没有。休息时和轻度运动时,两组受试者仰卧时的MSNA均低于坐姿。32%吸氧可降低HC的MSNA,但对HFrEF无影响。在两组中,高氧降低了低强度循环时爆发频率。高氧消除了HFrEF的“矛盾”交感神经兴奋。13名HFrEF患者在常规心肺康复4个月后进行了重新评估。运动训练在不改变CPB激活或PC抑制的情况下,使v_2峰值${{\dot{V}}_{{{{\mathrm{O}}} {2{\mathrm{峰值}}}}}}$提高17%,并减弱腿部MMR反应。我们得出结论,在HFrEF中,所有三种自主反射都不同程度地参与单腿循环。患者训练可减弱腿部MMR,但不影响运动期间CPB或PC对MSNA的调节。重点:在HFrEF患者中,在中等工作速率下单腿骑行时,夸张的腿部MMR是主要的交感神经兴奋反射;它们的MSNA响应与v_2峰${{\dot{V}}_{{{{\ mathm {O}}}_{2{\ mathm{峰}}}}}}$成反比。运动激活心肺调压反射和外周化学反射也有作用,这表明仰卧或呼吸32%氧气时进行运动可以补充传统的训练方案。以运动为基础的心脏康复方案通过消除腿部MMR反应来降低休息和轻度强度骑行时的交感放电。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of sympathetic excitation during cycling exercise in heart failure with reduced ejection fraction.

Leg muscle sympathetic nerve activity (MSNA) diminishes in healthy (HC) individuals during mild dynamic exercise but not in age-matched patients with heart failure due to reduced ejection fraction (HFrEF). To elucidate the neural mechanisms responsible for such sympathetic excitation, we studied 20 stable HFrEF patients (6F; mean age 62 ± 8 SD years) and 15 age-matched HC (6F; mean age 59 ± 7). We quantified peak oxygen uptake ( V ̇ O 2 peak ${{\dot{V}}_{{{{\mathrm{O}}}_{2{\mathrm{peak}}}}}}$ ) and separately, fibular MSNA (microneurography) at rest and during one-leg cycling (2 min each, mild (unloaded) and moderate intensity (loaded = 30-40% V ̇ O 2 peak ${{\dot{V}}_{{{{\mathrm{O}}}_{2{\mathrm{peak}}}}}}$ )) throughout three interventions: (1) post-exercise circulatory occlusion (PECO), which isolates the leg muscle metaboreflex (MMR); (2) supine posture, which stimulates cardiopulmonary baroreceptors (CPB); and (3) 32% inspired oxygen, to supress the peripheral chemoreflex (PC). One-leg cycling increased MSNA and activated the leg MMR in patients with HFrEF but not HC. MSNA at rest and during mild exercise was lower when supine than seated in both cohorts. Breathing 32% oxygen lowered the MSNA of HC but not HFrEF. In both groups, hyperoxia decreased burst frequency during low-intensity cycling. Hyperoxia abolished the 'paradoxical' sympatho-excitation of HFrEF. Thirteen participants with HFrEF were reassessed after 4 months of conventional cardiopulmonary rehabilitation. Exercise training improved V ̇ O 2 peak ${{\dot{V}}_{{{{\mathrm{O}}}_{2{\mathrm{peak}}}}}}$ by 17% and attenuated the leg MMR response without altering CPB activation or PC suppression. We conclude that in HFrEF, all three autonomic reflexes are engaged to a varying degree by one-leg cycling. Patient training attenuates the leg MMR without affecting CPB or PC modulation of MSNA during exercise. KEY POINTS: In HFrEF patients, an exaggerated leg MMR is the dominant sympatho-excitatory reflex during one-leg cycling at moderate work rates; with their MSNA response relating inversely to V ̇ O 2 peak ${{\dot{V}}_{{{{\mathrm{O}}}_{2{\mathrm{peak}}}}}}$ . Activation of the cardiopulmonary baroreflex and peripheral chemoreflex by exercise also contribute, suggesting that exercising supine or while breathing 32% O2 may complement conventional training protocols. An exercise-based cardiac rehabilitation programme lowers sympathetic discharge at rest and during mild intensity cycling by abolishing specifically the leg MMR response.

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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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