Langewitz W, Rüddel H, Schächinger H, Lepper W, Mulder L J, Veldman J H, van Roon A
Department of Medicine (Psychosomatic Medicine) University of Bonn, FRG.
Homeost Health Dis. 1991;33(1-2):23-33.
Spectral analyses of heart rate (HR) and blood pressure (BP) fluctuations yield three typical peaks at a low (0.02-0.06 Hz), a mid (0.07-0.14 Hz) and a high (around the respiratory frequency) frequency area. These so-called bands attract the interest of researchers because they seem to offer the facility of non-invasively studying autonomic cardiovascular control mechanisms. The high frequency component is solely under vagal control, the influence of sympathetic/vagal efferents on the low and mid frequency band is unclear. We therefore investigated in a single case study (23 year old male) the effects of propanol (0.06 mg/kg, 30 min. interruption, 0.12 mg/kg i.v.), dobutamine (1.14 micrograms/kg/min for 30 minutes, then 2.21 micrograms/kg/min i.v., then 4.42 micrograms/kg/min), atropine (0.01 mg/kg within 5 minutes, 30 minutes later 0.02 mg/kg within 5 minutes), and carbachol (0.125 mg, 30 min. interruption, 0.25 mg s.c.) upon HR, HR-variability spectra, BP and respiratory parameters at rest and during 5 minutes of a mental task. Under all four drug conditions BP is elevated at rest and mental stress, the latter always giving higher results than the former. Atropine shortens interbeat intervals (IBI) by almost 50 percent (from 939 msec to 514 msec), the high dose of dobutamine reduces IBI from 725 to 580 msec, propranolol increases interval length by 10 percent. Drug effects on spectral bands give clear results with atropine: It reduces spectral energy in all three frequency bands at rest and during mental stress. The other drugs show no clear-cut effects on HR-variability spectra. Even though results of a single case study should be interpreted with great caution we believe that the following conclusion can be made: At rest and during short-lasting mental stress all frequency bands in HR-variability spectra are to a large extent under parasympathetic control.
心率(HR)和血压(BP)波动的频谱分析在低频(0.02 - 0.06赫兹)、中频(0.07 - 0.14赫兹)和高频(接近呼吸频率)区域产生三个典型峰值。这些所谓的频段引起了研究人员的兴趣,因为它们似乎提供了非侵入性研究自主心血管控制机制的便利。高频成分仅受迷走神经控制,交感神经/迷走神经传出纤维对低频和中频带的影响尚不清楚。因此,我们在一项单病例研究(23岁男性)中,研究了普萘洛尔(0.06毫克/千克,中断30分钟,静脉注射0.12毫克/千克)、多巴酚丁胺(1.14微克/千克/分钟,持续30分钟,然后静脉注射2.21微克/千克/分钟,然后4.42微克/千克/分钟)、阿托品(5分钟内0.01毫克/千克,30分钟后5分钟内0.02毫克/千克)和卡巴胆碱(0.125毫克,中断30分钟,皮下注射0.25毫克)对静息状态以及在进行5分钟心理任务期间的心率、心率变异性频谱、血压和呼吸参数的影响。在所有四种药物条件下,静息和心理应激时血压均升高,心理应激时的结果总是高于静息时。阿托品使心跳间期(IBI)缩短近50%(从939毫秒降至514毫秒),高剂量多巴酚丁胺使IBI从725毫秒降至580毫秒,普萘洛尔使间期长度增加10%。药物对频谱带的影响在阿托品作用下结果明确:静息和心理应激时,它降低了所有三个频段的频谱能量。其他药物对心率变异性频谱没有明确的影响。尽管单病例研究的结果应极为谨慎地解释,但我们认为可以得出以下结论:在静息和短暂心理应激期间,心率变异性频谱中的所有频段在很大程度上受副交感神经控制。