Tantucci C, Scionti L, Bottini P, Dottorini M L, Puxeddu E, Casucci G, Sorbini C A
Clinica di Semeiotica e Metodologia Medica, University of Ancona, Italy.
Chest. 1997 Jul;112(1):145-53. doi: 10.1378/chest.112.1.145.
To investigate the effects of the autonomic nervous system on control of breathing, the neuromuscular (mouth occlusion pressure at 0.1 s after onset of inspiration [P0.1]) and ventilatory (minute ventilation [VE]) response to progressive hyperoxic hypercapnia was assessed in diabetic patients with autonomic dysfunction of different severity. Eighteen diabetics with autonomic neuropathy, nine with parasympathetic damage (DANp), and nine with parasympathetic and sympathetic damage (DANp+s), as indicated by marked postural hypotension, low increment of diastolic BP during sustained handgrip, and lowest resting catecholamine plasma levels, were studied together with a group of 10 diabetic patients without autonomic neuropathy (D) and a group of 10 normal subjects (C). All subjects had pulmonary function tests, including maximal voluntary ventilation and diffusion of carbon monoxide, measurements of respiratory muscle strength as maximal inspiratory mouth pressure (MIP) and maximal expiratory mouth pressure (MEP), and a CO2 rebreathing test (Read's method). Although in the normal range, lung volumes and FEV1 and forced expiratory flows were lower in the DANp and DANp+s groups than in the D and C groups, MIP and MEP were similar among C and diabetic groups, as well as resting P0.1, VE, tidal volume (VT), and respiratory rate (RR). The slope of the linear relationship between P0.1 and end-tidal PCO2 (PETCO2) was higher in DANp+s (0.63+/-0.07 cm H2O/mm Hg) than in C (0.45+/-0.06 cm H2O/mm Hg; p<0.05) and three times greater in DANp+s than in D (0.26+/-0.03 cm H2O/mm Hg; p<0.001) and DANp (0.24+/-0.03 cm H2O/mm Hg; p<0.001), who in turn showed a lower deltaP0.1/deltaPETCO2 than C. The VE increase with increasing PETCO2 was greater in DANp+s (3.70+/-0.85 L/min/mm Hg) than in DANp (2.13+/-0.20 L/min/mm Hg; p<0.05) and D (2.37+/-0.40 L/min/mm Hg; p=0.07), but not significantly higher from that of C (3.17+/-0.36 L/min/mm Hg). No differences were found for deltaVT/deltaPETCO2 among the groups, whereas the deltaRR/deltaPETCO2 relationship was steeper in DANp+s than in DANp (p<0.05) and D (p=0.055). These data reflect a depressed CO2 response both in D and DANp. The presumable decrease of the sympathetic nerve traffic in DANp+s appears to reverse this abnormality. DANp+s, however, exhibit an enhanced CO2 neuromuscular response even in respect to C, suggesting that the sympathetic nervous system might modulate the output of the respiratory centers to hypercapnic stimulus.
为研究自主神经系统对呼吸控制的影响,我们评估了不同严重程度自主神经功能障碍的糖尿病患者对渐进性高氧高碳酸血症的神经肌肉反应(吸气开始后0.1秒时的口腔闭塞压[P0.1])和通气反应(分钟通气量[VE])。研究对象包括18例患有自主神经病变的糖尿病患者、9例伴有副交感神经损伤的患者(DANp)以及9例伴有副交感神经和交感神经损伤的患者(DANp + s),这些患者表现为明显的体位性低血压、持续握力时舒张压升高幅度低以及静息时血浆儿茶酚胺水平最低,同时还纳入了10例无自主神经病变的糖尿病患者(D)组和10例正常受试者(C)组。所有受试者均进行了肺功能测试,包括最大自主通气量和一氧化碳弥散量,测量呼吸肌力量,即最大吸气口腔压力(MIP)和最大呼气口腔压力(MEP),以及二氧化碳再呼吸试验(Read法)。尽管在正常范围内,但DANp组和DANp + s组的肺容积、第一秒用力呼气容积(FEV1)和用力呼气流量均低于D组和C组,而C组与糖尿病组之间的MIP和MEP相似,静息P0.1、VE、潮气量(VT)和呼吸频率(RR)也相似。DANp + s组中P0.1与呼气末二氧化碳分压(PETCO2)之间线性关系的斜率(0.63±0.07 cm H2O/mm Hg)高于C组(0.45±0.06 cm H2O/mm Hg;p<0.05),且DANp + s组是D组(0.26±0.03 cm H2O/mm Hg;p<0.001)和DANp组(0.24±0.03 cm H2O/mm Hg;p<0.001)的三倍,而D组和DANp组的ΔP0.1/ΔPETCO2低于C组。随着PETCO2升高,DANp + s组的VE增加幅度(3.70±0.85 L/min/mm Hg)大于DANp组(2.13±0.20 L/min/mm Hg;p<0.05)和D组(2.37±0.40 L/min/mm Hg;p = 0.07),但与C组(3.17±0.36 L/min/mm Hg)相比无显著差异。各组间的ΔVT/ΔPETCO2无差异,而DANp + s组中ΔRR/ΔPETCO2的关系比DANp组(p<0.05)和D组(p = 0.055)更陡峭。这些数据反映了D组和DANp组中二氧化碳反应均降低。DANp + s组中交感神经活动可能的降低似乎逆转了这种异常。然而,即使与C组相比,DANp + s组仍表现出增强的二氧化碳神经肌肉反应,这表明交感神经系统可能调节呼吸中枢对高碳酸血症刺激的输出。