Furlan R, Piazza S, Bevilacqua M, Turiel M, Norbiato G, Lombardi F, Malliani A
Centro Ricerche Cardiovascolari, CNR, Milano, Italy.
J Auton Nerv Syst. 1995 Mar 2;51(3):223-35. doi: 10.1016/0165-1838(94)00135-7.
The aim of this study was to evaluate the sympatho-vagal interaction modulating cardiovascular function and the possible impairment of baroreceptor sensitivity in patients affected by Pure Autonomic Failure (PAF). We studied 4 patients affected by PAF and 7 controls at rest and during different levels (45 degrees, 60 degrees, 90 degrees) of head-up tilt. On a different day all subjects underwent i.v. administration of phenylephrine at dosages adequate to enhance systolic blood pressure by about 20 mmHg both at rest and during 45 degrees head-up tilt. Finally, 1.5 mg atropine was infused intravenously only in the patients. Spectral analysis of RR interval and systolic arterial pressure (SAP) variabilities provided markers of sympathetic (low-frequency oscillations, about 0.1 Hz, LFRR) and vagal (high-frequency oscillations, about 0.25 Hz, HFRR) modulations of heart period and of sympathetic vasomotor activity (low-frequency oscillations of SAP variability, LFSAP). Baroreceptor mechanisms were quantified by means of the index alpha (calculated from the square root of the ratio between the powers of HF components of RR interval and SAP variabilities) and of the phenylephrine RR-SAP slope. Patients affected by PAF were characterized by a drastic decrease in total power of RR variability and by the absence of LFRR and LFSAP components. Moreover, HFRR, although largely predominant in its relative value, was also markedly reduced in its absolute value. Finally, the baroreceptive mechanisms appeared to be heavily impaired. In conclusion, PAF patients seem to be characterized by a complex alteration of neural mechanisms, which in addition to the signs of a sympathetic denervation include an impairment, at least functional, of the vagal modulation of heart rate.
本研究旨在评估纯自主神经功能衰竭(PAF)患者中调节心血管功能的交感-迷走神经相互作用以及压力感受器敏感性可能存在的损害。我们研究了4例PAF患者和7例对照者,分别在静息状态以及不同程度(45度、60度、90度)的头高位倾斜过程中进行观察。在另一天,所有受试者静脉注射去氧肾上腺素,剂量足以使静息状态及45度头高位倾斜时收缩压升高约20 mmHg。最后,仅对患者静脉注射1.5 mg阿托品。RR间期和收缩期动脉压(SAP)变异性的频谱分析提供了心脏周期交感神经(低频振荡,约0.1 Hz,LFRR)和迷走神经(高频振荡,约0.25 Hz,HFRR)调节以及交感血管运动活动(SAP变异性的低频振荡,LFSAP)的标志物。通过指数α(由RR间期和SAP变异性的高频成分功率之比的平方根计算得出)和去氧肾上腺素RR-SAP斜率对压力感受器机制进行量化。PAF患者的特征是RR变异性的总功率急剧下降,且不存在LFRR和LFSAP成分。此外,HFRR虽然在相对值上占主导地位,但其绝对值也明显降低。最后,压力感受机制似乎严重受损。总之,PAF患者似乎具有神经机制的复杂改变,除了交感神经去神经支配的迹象外,还包括至少在功能上迷走神经对心率调节的损害。