Department of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, Utah, United States.
Division of Geriatrics, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, United States.
Am J Physiol Heart Circ Physiol. 2023 Oct 1;325(4):H806-H813. doi: 10.1152/ajpheart.00450.2023. Epub 2023 Aug 11.
Exercising muscle blood flow is reduced in patients with heart failure with a preserved ejection fraction (HFpEF), which may be related to disease-related changes in the ability to overcome sympathetic nervous system (SNS)-mediated vasoconstriction during exercise, (i.e., "functional sympatholysis"). Thus, in 12 patients with HFpEF (69 ± 7 yr) and 11 healthy controls (Con, 69 ± 4 yr), we examined forearm blood flow (FBF), mean arterial pressure (MAP), and forearm vascular conductance (FVC) during rhythmic handgrip exercise (HG) at 30% of maximum voluntary contraction with or without lower-body negative pressure (LBNP, -20 mmHg) to increase SNS activity and elicit peripheral vasoconstriction. SNS-mediated vasoconstrictor responses were determined as LBNP-induced changes (%Δ) in FVC, and the "magnitude of sympatholysis" was calculated as the difference between responses at rest and during exercise. At rest, the LBNP-induced change in FVC was significantly lesser in HFpEF compared with Con (HFpEF: -9.5 ± 5.5 vs. Con: -21.0 ± 8.0%; < 0.01). During exercise, LBNP-induced %ΔFVC was significantly attenuated in Con compared with rest (HG: -5.8 ± 6.0%; < 0.05) but not in HFpEF (HG: -9.9 ± 2.5%; = 0.88). Thus, the magnitude of sympatholysis was lesser in HFpEF compared with Con (HFpEF: 0.4 ± 4.7 vs. Con: -15.2 ± 11.8%; < 0.01). These data demonstrate a diminished ability to attenuate SNS-mediated vasoconstriction in HFpEF and provide new evidence suggesting impaired functional sympatholysis in this patient group. Data from the current study suggest that functional sympatholysis, or the ability to adequately attenuate sympathetic nervous system (SNS)-mediated vasoconstriction during exercise, is impaired in patients with heart failure with preserved ejection fraction (HFpEF). These observations extend the current understanding of HFpEF pathophysiology by implicating inadequate functional sympatholysis as an important contributor to reduced exercising muscle blood flow in this patient group.
在射血分数保留的心力衰竭(HFpEF)患者中,运动肌肉的血流量减少,这可能与疾病相关的改变有关,即在运动期间克服交感神经系统(SNS)介导的血管收缩的能力(即“功能性交感神经溶解”)。因此,我们在 12 名 HFpEF 患者(69±7 岁)和 11 名健康对照者(Con,69±4 岁)中,检查了在 30%最大自主收缩力的节律性握力运动(HG)期间的前臂血流(FBF)、平均动脉压(MAP)和前臂血管传导性(FVC),同时施加下肢负压(LBNP,-20mmHg)以增加 SNS 活动并引起外周血管收缩。SNS 介导的血管收缩反应被确定为 LBNP 诱导的 FVC 变化(%Δ),并且“交感神经溶解的程度”被计算为静息和运动期间的反应之间的差异。在静息状态下,HFpEF 中 LBNP 诱导的 FVC 变化明显小于 Con(HFpEF:-9.5±5.5 比 Con:-21.0±8.0%; <0.01)。在运动过程中,与静息相比,Con 中 LBNP 诱导的%ΔFVC 明显减弱(HG:-5.8±6.0%; <0.05),但 HFpEF 中没有减弱(HG:-9.9±2.5%; =0.88)。因此,HFpEF 中的交感神经溶解程度明显小于 Con(HFpEF:0.4±4.7 比 Con:-15.2±11.8%; <0.01)。这些数据表明 HFpEF 中 SNS 介导的血管收缩的减弱能力降低,并提供了新的证据表明该患者群体中存在受损的功能性交感神经溶解。当前研究的数据表明,在射血分数保留的心力衰竭(HFpEF)患者中,功能性交感神经溶解或在运动期间充分减弱交感神经系统(SNS)介导的血管收缩的能力受损。这些观察结果通过表明在该患者组中,运动肌肉血流量减少的重要原因是功能性交感神经溶解不足,从而扩展了 HFpEF 病理生理学的现有认识。