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兔膈肌的传递性疲劳

Transmission fatigue of the rabbit diaphragm.

作者信息

Aldrich T K

机构信息

Department of Medicine, Montefiore Medical Center, Bronx, NY 10467.

出版信息

Respir Physiol. 1987 Sep;69(3):307-19. doi: 10.1016/0034-5687(87)90085-5.

Abstract

This study evaluates the role of transmission fatigue of the diaphragm in rabbits subjected to inspiratory resistive loading (IRL) sufficiently severe to increase peak tidal airway pressure to about 50% of that elicited by 100 Hz phrenic nerve stimulation. After 58 +/- 14 min of IRL, the transdiaphragmatic pressure (Pdi) responses to phrenic nerve stimulation at 20, 60, and 100 Hz were reduced by approximately one third. In contrast, IRL induced no significant change in the response to direct diaphragm stimulation (in the presence of transient neuromuscular blockade). Although respiratory acidosis occurred during IRL (pH 7.04 +/- 0.04, PCO2 90 +/- 10, PO2 131 +/- 38), it was not sufficient to explain the reduced contractility. In a separate series of experiments, the diaphragm compound action potential elicited by unilateral phrenic nerve stimuli was recorded by implanted diaphragm electrodes and the Pdi elicited by contralateral phrenic nerve stimulation at 100 Hz was measured. Both action potential amplitude and Pdi declined during IRL and both improved after 10 min of recovery. These findings demonstrate that transmission fatigue plays a major role in rabbit diaphragm fatigue induced by spontaneous breathing against inspiratory resistance.

摘要

本研究评估了在承受吸气阻力负荷(IRL)的家兔中,膈肌传导性疲劳所起的作用。该负荷严重到足以使潮气量峰值气道压力增加至由100Hz膈神经刺激所引发压力的约50%。在IRL持续58±14分钟后,膈神经在20Hz、60Hz和100Hz刺激下的跨膈压(Pdi)反应降低了约三分之一。相比之下,IRL对直接膈肌刺激的反应(在存在短暂神经肌肉阻滞的情况下)未引起显著变化。尽管在IRL期间出现了呼吸性酸中毒(pH 7.04±0.04,PCO2 90±10,PO2 131±38),但这不足以解释收缩力的降低。在另一系列实验中,通过植入的膈肌电极记录单侧膈神经刺激引发的膈肌复合动作电位,并测量对侧膈神经在100Hz刺激下引发的Pdi。在IRL期间,动作电位幅度和Pdi均下降,恢复10分钟后两者均有所改善。这些发现表明,传导性疲劳在因对抗吸气阻力进行自主呼吸而导致的家兔膈肌疲劳中起主要作用。

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