Sheel A William, Derchak P Alexander, Pegelow David F, Dempsey Jerome A
University of Wisconsin-Madison, Department of Population Health Sciences, John Rankin Laboratory of Pulmonary Medicine, Madison, Wisconsin 53705, USA.
Am J Physiol Heart Circ Physiol. 2002 May;282(5):H1732-8. doi: 10.1152/ajpheart.00798.2001.
The purpose of this study was to determine whether the human diaphragm, like limb muscle, has a threshold of force output at which a metaboreflex is activated causing systemic vasoconstriction. We used Doppler ultrasound techniques to quantify leg blood flow (Q(L)) and utilized the changes in mouth twitch pressure (DeltaP(M)T) in response to bilateral phrenic nerve stimulation to quantify the onset of diaphragm fatigue. Six healthy male subjects performed four randomly assigned trials of identical duration (8 +/- 2 min) and breathing pattern [20 breaths/min and time spent on inspiration during the duty cycle (time spent on inspiration/total time of one breathing cycle) was 0.4] during which they inspired primarily with the diaphragm. For trials 1-3, inspiratory resistance and effort was gradually increased [30, 40, and 50% maximal inspiratory pressure (MIP)], diaphragm fatigue did not occur, and Q(L), limb vascular resistance (LVR), and mean arterial pressure remained unchanged from control (P > 0.05). The fourth trial utilized the same breathing pattern with 60% MIP and caused diaphragm fatigue, as shown by a 30 +/- 12% reduction in P(M)T with bilateral phrenic nerve stimulation. During the fatigue trial, Q(L) and LVR were unchanged from baseline at minute 1, but LVR rose 36% and Q(L) fell 25% at minute 2 and by 52% and 30%, respectively, during the final minutes of the trial. Both LVR and Q(L) returned to control within 30 s of recovery. In summary, voluntary increases in inspiratory muscle effort, in the absence of fatigue, had no effect on LVR and Q(L), whereas fatiguing the diaphragm elicited time-dependent increases in LVR and decreases in Q(L). We attribute the limb vasoconstriction to a metaboreflex originating in the diaphragm, which reaches its threshold for activation during fatiguing contractions.
本研究的目的是确定人类膈肌是否像肢体肌肉一样,存在一个力输出阈值,在该阈值时会激活代谢性反射,导致全身血管收缩。我们使用多普勒超声技术来量化腿部血流量(Q(L)),并利用双侧膈神经刺激后口部抽搐压力(DeltaP(M)T)的变化来量化膈肌疲劳的开始。六名健康男性受试者进行了四项随机分配的试验,试验持续时间相同(8±2分钟)且呼吸模式相同[20次/分钟,吸气时间占呼吸周期的比例(吸气时间/一个呼吸周期的总时间)为0.4],在此期间他们主要通过膈肌吸气。在试验1 - 3中,吸气阻力和努力程度逐渐增加[分别为最大吸气压力(MIP)的30%、40%和50%],未出现膈肌疲劳,Q(L)、肢体血管阻力(LVR)和平均动脉压与对照组相比保持不变(P>0.05)。第四次试验采用相同的呼吸模式,MIP为60%,导致了膈肌疲劳,双侧膈神经刺激时P(M)T降低了30±12%,表明出现了膈肌疲劳。在疲劳试验中,第1分钟时Q(L)和LVR与基线相比无变化,但在第2分钟时LVR上升了36%,Q(L)下降了25%,在试验的最后几分钟分别上升了52%和下降了30%。LVR和Q(L)在恢复30秒内均恢复到对照水平。总之,在没有疲劳的情况下,吸气肌努力程度的自愿增加对LVR和Q(L)没有影响,而膈肌疲劳会引起LVR随时间增加和Q(L)降低。我们将肢体血管收缩归因于起源于膈肌的代谢性反射,该反射在疲劳收缩期间达到激活阈值。