年轻高血压患者静息和运动时的颈动脉化学反射控制。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Thomas Hinton, Katrina Hope, Zoe Adams, Lydia L. Simpson, Julian F. R. Paton, Adrian Kendrick, Ana P. Abdala, Hazel Blythe, Angus K. Nightingale, Emma C. Hart
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引用次数: 0

摘要

尽管有报道称年轻高血压患者的颈动脉对缺氧的化学反射敏感性增强(V²O峰值${\dot V_{{\ mathm {O}}_2}{\ mathm{峰值}}}}$)。采用双盲安慰剂对照全身输注低剂量多巴胺(2 mcg/kg/min)来抑制颈动脉化学反射,并评估其在休息和亚极限运动时对通气和血压的促进作用(混合模型方差分析)。静息和亚最大周期运动时的低氧通气反应(HVR)在两组之间具有可比性,多巴胺输注也同样使两组的低氧通气反应(HVR)减弱。然而,在静息时,HTN组颈动脉化学反射抑制期间的静息收缩压(SBP)下降幅度更大。值得注意的是,在亚极限运动中,多巴胺组与生理盐水组相比,收缩压降低,但两组之间的下降相似。在未治疗HTN的年轻人中,颈动脉化学反射似乎有助于静息收缩压,但在该组中,没有在夸大的运动血压反应中发挥作用。重点:颈动脉化学反射在未治疗高血压的年轻成人维持高静息和运动血压中的作用尚不清楚。通过缺氧通气反应评估的颈动脉化学反射敏感性在未经治疗的年轻高血压患者(n = 14,年龄)之间相似
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Carotid chemoreflex control of blood pressure at rest and during exercise in young-onset hypertension

Carotid chemoreflex control of blood pressure at rest and during exercise in young-onset hypertension
Despite reports of amplified carotid chemoreflex sensitivity to hypoxia in young adults with hypertension (<40 years), it is unclear whether this equates to a direct role of this reflex in maintaining high resting and exercise blood pressures (BP). The aim of this study was to examine whether tonic carotid chemoreflex activity contributes to high resting and exercise BP in young people with untreated hypertension compared to normotensives (NTN). In 14 NTN and 14 untreated hypertensives (HTN) (aged 27 ± 6 and 28 ± 5 years, respectively) the ventilatory and haemodynamic responses to hypoxia were measured using the transient hypoxic test at rest and during submaximal steady-state upright cycle exercise (40%–50% V ̇ O 2 peak ${\dot V_{{{\mathrm{O}}_2}{\mathrm{peak}}}}$ ). A double-blinded placebo-controlled systemic infusion of low-dose dopamine (2 mcg/kg/min) was used to inhibit the carotid chemoreflex and assess its tonic contribution to ventilation and BP at rest and submaximal exercise (mixed-model ANOVA). The hypoxic ventilatory response (HVR) at rest and submaximal cycle exercise were comparable between groups and were similarly blunted by dopamine infusion in both groups. However, at rest, there was a greater decrease in resting systolic BP (SBP) during carotid chemoreflex inhibition in the HTN group. Notably, during submaximal exercise, SBP was reduced during dopamine versus that during saline, but the decrease was similar between groups. The carotid chemoreflex appears to contribute to resting SBP in young people with untreated HTN but does not play a role in exaggerated exercise BP responses in this group.

Key points

  • The role of the carotid chemoreflex in maintaining high resting and exercise blood pressures in young adults with untreated hypertension is unclear.
  • Carotid chemoreflex sensitivity, assessed by the ventilatory response to hypoxia was similar between untreated young adults with hypertension (n = 14, age < 40 years) and age-matched normotensives (n = 14).
  • During normoxic rest, there was a reduction in SBP during carotid chemoreflex inhibition with low-dose dopamine (2 mcg/kg/min; vs. saline) in people with hypertension which was not observed in the normotensive group.
  • During submaximal cycle exercise, SBP was reduced during carotid chemoreflex inhibition, but this was similar between groups.
  • These results suggest the carotid chemoreflex influences resting SBP in hypertensives but does not affect the exaggerated exercise BP response in this group.
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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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