首页> 美国卫生研究院文献>American Journal of Physiology - Heart and Circulatory Physiology >Chronic baroreflex activation restores spontaneous baroreflex control and variability of heart rate in obesity-induced hypertension
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Chronic baroreflex activation restores spontaneous baroreflex control and variability of heart rate in obesity-induced hypertension

机译:肥胖引起的高血压中的慢性压力反射激活可恢复自发的压力反射控制和心率变异性

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摘要

The sensitivity of baroreflex control of heart rate is depressed in subjects with obesity hypertension, which increases the risk for cardiac arrhythmias. The mechanisms are not fully known, and there are no therapies to improve this dysfunction. To determine the cardiovascular dynamic effects of progressive increases in body weight leading to obesity and hypertension in dogs fed a high-fat diet, 24-h continuous recordings of spontaneous fluctuations in blood pressure and heart rate were analyzed in the time and frequency domains. Furthermore, we investigated whether autonomic mechanisms stimulated by chronic baroreflex activation and renal denervation—current therapies in patients with resistant hypertension, who are commonly obese—restore cardiovascular dynamic control. Increases in body weight to ∼150% of control led to a gradual increase in mean arterial pressure to 17 ± 3 mmHg above control (100 ± 2 mmHg) after 4 wk on the high-fat diet. In contrast to the gradual increase in arterial pressure, tachycardia, attenuated chronotropic baroreflex responses, and reduced heart rate variability were manifest within 1–4 days on high-fat intake, reaching 130 ± 4 beats per minute (bpm) (control = 86 ± 3 bpm) and ∼45% and <20%, respectively, of control levels. Subsequently, both baroreflex activation and renal denervation abolished the hypertension. However, only baroreflex activation effectively attenuated the tachycardia and restored cardiac baroreflex sensitivity and heart rate variability. These findings suggest that baroreflex activation therapy may reduce the risk factors for cardiac arrhythmias as well as lower arterial pressure.
机译:在肥胖症高血压患者中,压力反射控制心率的敏感性降低,这增加了心律不齐的风险。其机制尚不完全清楚,也没有疗法可改善这种功能障碍。为了确定高脂饮食狗的体重逐渐增加导致肥胖和高血压的心血管动力学效应,在时域和频域对血压和心率的自发性波动进行了24小时连续记录。此外,我们研究了慢性压力反射反射激活和肾脏去神经支配所刺激的自主神经机制(目前对于肥胖的抵抗性高血压患者的当前治疗方法)是否能恢复心血管动态控制。体重增加至约150%的对照后,高脂饮食4周后平均动脉压逐渐比对照(100±2 mmHg)逐渐增加至17±3 mmHg。与逐渐增加的动脉压相反,高脂饮食在1至4天内表现为心动过速,变时性压力反射反应减弱和心率变异性降低,达到每分钟130±4次搏动(bpm)(对照= 86± 3 bpm),分别为对照水平的〜45%和<20%。随后,压力反射激活和肾神经支配都消除了高血压。但是,只有压力反射激活才能有效地减弱心动过速并恢复心脏压力反射敏感性和心率变异性。这些发现表明压力反射激活疗法可以减少心律不齐以及降低动脉压的危险因素。

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