Chang F C
Pathophysiology Division, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010-5425.
Brain Res Bull. 1991 Jan;26(1):123-32. doi: 10.1016/0361-9230(91)90196-q.
Respiratory effects of sodium pentobarbital (35 mg/kg; IP) were studied in guinea pigs chronically instrumented to permit concurrent recordings of bulbar respiratory-related units (RRUs), diaphragmatic electromyogram (DEMG), and electrocorticogram (ECoG). RRU activities were recorded from either the Bötzinger Complex (BOT; expiratory) or Nucleus para-Ambiguus (NpA; inspiratory). Pentobarbital-induced changes in respiratory-related activities were evaluated before, throughout the course of, and during recovery from, anesthesia. The most notable development following pentobarbital was a state of progressive bradypnea which was accompanied by a variety of complex changes in the amplitude and temporal attributes of RRU, DEMG and ECoG activities. As anesthetic effects progressed, the activity profiles of both BOT and NpA units underwent striking transformations from a behavioral and state-dependent wakefulness pattern to an activity profile characterized by i) a significantly augmented RRU cycle duration, burst duration and spike frequency; and, ii) an alteration to the pattern of within-burst spike frequency modulation. Along with changes in RRU activity, pentobarbital also produced a marked attenuation of the amplitudes of diaphragmatic activity as well as a discrete, time-dependent alteration in the amplitude and spectral characters of ECoG activities. Differences in BOT and NpA unit responses to alveolar CO2 loading (ramp; 2% and 5%) across wakefulness and anesthesia states were also considerable. In addition to a depressed responsiveness to CO2, the temporal attributes of BOT and NpA activity profiles also indicated an asymmetrical change under pentobarbital anesthesia. Taken together, these findings indicate that pentobarbital causes not only a fundamental alteration in bulbar rhythmogenic mechanisms, but also a differential influence on bulbar respiratory system components that are involved in the definition of the shape and the amplitude of central respiratory drive. In conclusion, this study offers, for the first time, direct evidence from physiologically and structurally intact preparations that the functional dynamics of respiratory system components are profoundly altered during pentobarbital anesthesia.
在慢性植入仪器的豚鼠中研究了戊巴比妥钠(35毫克/千克;腹腔注射)的呼吸效应,以便同时记录延髓呼吸相关单位(RRU)、膈肌肌电图(DEMG)和脑电图(ECoG)。RRU活动记录于包钦格复合体(BOT;呼气)或疑核旁核(NpA;吸气)。在麻醉前、麻醉过程中和麻醉恢复期间评估戊巴比妥引起的呼吸相关活动变化。戊巴比妥给药后最显著的变化是进行性呼吸过缓状态,同时RRU、DEMG和ECoG活动的幅度和时间属性发生了各种复杂变化。随着麻醉效果的进展,BOT和NpA单位的活动模式经历了显著转变,从行为和状态依赖的清醒模式转变为具有以下特征的活动模式:i)RRU周期持续时间、爆发持续时间和尖峰频率显著增加;ii)爆发内尖峰频率调制模式改变。随着RRU活动的变化,戊巴比妥还使膈肌活动幅度显著减弱,以及ECoG活动幅度和频谱特征随时间发生离散变化。在清醒和麻醉状态下,BOT和NpA单位对肺泡二氧化碳负荷(斜坡;2%和5%)的反应差异也相当大。除了对二氧化碳的反应性降低外,BOT和NpA活动模式的时间属性在戊巴比妥麻醉下也显示出不对称变化。综上所述,这些发现表明戊巴比妥不仅引起延髓节律产生机制的根本改变,而且对参与定义中枢呼吸驱动形状和幅度的延髓呼吸系统成分产生不同影响。总之,本研究首次从生理和结构完整的制剂中提供了直接证据,表明戊巴比妥麻醉期间呼吸系统成分的功能动力学发生了深刻改变。