Babcock Matthew C, Brian Michael S, Watso Joseph C, Edwards David G, Stocker Sean D, Wenner Megan M, Farquhar William B
Department of Kinesiology and Applied Physiology, University of Delaware , Newark, Delaware.
Department of Health and Human Performance, Plymouth State University , Plymouth, New Hampshire.
Am J Physiol Regul Integr Comp Physiol. 2018 Oct 1;315(4):R688-R695. doi: 10.1152/ajpregu.00002.2018. Epub 2018 Jun 27.
High dietary sodium intake has been linked to alterations in neurally mediated cardiovascular function, but the effects of high sodium on cardiovagal baroreflex sensitivity (cBRS) in healthy adults are unknown. The purpose of this study was to determine whether high dietary sodium alters cBRS and heart rate variability (HRV) and whether acute intravenous sodium loading similarly alters cBRS and HRV. High dietary sodium (300 mmol/day, 7 days) was compared with low dietary sodium (20 mmol/day, 7 days; randomized) in 14 participants (38 ± 4 yr old, 23 ± 1 kg/m body mass index, 7 women). Acute sodium loading was achieved via a 23-min intravenous hypertonic saline infusion (HSI) in 14 participants (22 ± 1 yr old, 23 ± 1 kg/m body mass index, 7 women). During both protocols, participants were supine for 5 min during measurement of beat-to-beat blood pressure (photoplethysmography) and R-R interval (ECG). cBRS was evaluated using the sequence method. Root mean square of successive differences in R-R interval (RMSSD) was used as an index of HRV. Serum sodium (137.4 ± 0.7 vs. 139.9 ± 0.5 meq/l, P < 0.05), plasma osmolality (285 ± 1 vs. 289 ± 1 mosmol/kgHO, P < 0.05), cBRS (18 ± 2 vs. 26 ± 3 ms/mmHg, P < 0.05), and RMSSD (62 ± 6 vs. 79 ± 10 ms, P < 0.05) were increased following high-sodium diet intake compared with low-sodium diet intake. HSI increased serum sodium (138.1 ± 0.4 vs. 141.1 ± 0.5 meq/l, P < 0.05) and plasma osmolality (286 ± 1 vs. 290 ± 1 mosmol/kgHO, P < 0.05) but did not change cBRS (26 ± 5 vs. 25 ± 3 ms/mmHg, P = 0.73) and RMSSD (63 ± 9 vs. 63 ± 8 ms, P = 0.99). These data suggest that alterations in dietary sodium intake alter cBRS and HRV but that acute intravenous sodium loading does not alter these indexes of autonomic cardiovascular regulation.
高膳食钠摄入量与神经介导的心血管功能改变有关,但高钠对健康成年人心脏迷走神经压力反射敏感性(cBRS)的影响尚不清楚。本研究的目的是确定高膳食钠是否会改变cBRS和心率变异性(HRV),以及急性静脉注射钠负荷是否会同样改变cBRS和HRV。在14名参与者(年龄38±4岁,体重指数23±1kg/m²,7名女性)中,将高膳食钠(300 mmol/天,7天)与低膳食钠(20 mmol/天,7天;随机分组)进行比较。通过在14名参与者(年龄22±1岁,体重指数23±1kg/m²,7名女性)中进行23分钟的静脉高渗盐水输注(HSI)来实现急性钠负荷。在两个方案期间,参与者在测量逐搏血压(光电容积描记法)和R-R间期(心电图)时仰卧5分钟。使用序列法评估cBRS。R-R间期连续差值的均方根(RMSSD)用作HRV的指标。与低钠饮食摄入相比,高钠饮食摄入后血清钠(137.4±0.7 vs. 139.9±0.5 meq/l,P<0.05)、血浆渗透压(285±1 vs. 289±1 mosmol/kgH₂O,P<0.05)、cBRS(18±2 vs. 26±3 ms/mmHg,P<0.05)和RMSSD(62±6 vs. 79±10 ms,P<0.05)均升高。HSI增加了血清钠(138.1±0.4 vs. 141.1±0.5 meq/l,P<0.05)和血浆渗透压(286±1 vs. 290±1 mosmol/kgH₂O,P<0.05),但未改变cBRS(26±5 vs. 25±3 ms/mmHg,P=0.73)和RMSSD(63±9 vs. 63±8 ms,P=0.99)。这些数据表明,膳食钠摄入量的改变会改变cBRS和HRV,但急性静脉注射钠负荷不会改变这些自主心血管调节指标。