de Boisblanc B P, Meszaros K, Cairo J, Spitzer J J, Summer W
Department of Medicine, Louisiana State University, School of Medicine, New Orleans 70112.
J Med. 1990;21(1-2):7-26.
A rat model was used to study the effects of endotoxemic shock in vivo on diaphragmatic tension generation and diaphragmatic metabolism in vitro. Animals were injected with E. coli lipopolysaccharide (30 mg/kg) and killed at fixed times after injection. The hemidiaphragms were isolated in an organ bath, and tension generation was measured during electrical stimulation of the phrenic nerve or diaphragmatic muscle. Diaphragmatic oxygen consumption was measured in vitro during rest and during in vivo stimulation. Adenosine triphosphate and glycogen concentrations were measured in vivo before the animals were killed and in vitro. Tension generation was reduced in a time-dependent fashion after endotoxin at all stimulation frequencies. Both contractile fatigue and transmission fatigue were present. Glycogen stores were reduced but not depleted. ATP concentration was reduced in vivo but recovered in vitro. Diaphragmatic oxygen consumption was reduced in vitro at rest and during stimulation. The results suggest that endotoxemic shock results in diaphragmatic fatigue in a time-dependent fashion, that impaired neural or neuromuscular transmission is present in vitro, and that impaired oxygen consumption in the shocked diaphragm is associated with reduced high-energy-phosphate stores.
使用大鼠模型研究体内内毒素血症休克对体外膈肌张力产生和膈肌代谢的影响。给动物注射大肠杆菌脂多糖(30mg/kg),并在注射后的固定时间处死。将半侧膈肌分离置于器官浴槽中,在膈神经或膈肌电刺激期间测量张力产生。在体外休息期间和体内刺激期间测量膈肌耗氧量。在处死动物前和体外测量三磷酸腺苷和糖原浓度。内毒素作用后,在所有刺激频率下,张力产生均呈时间依赖性降低。同时存在收缩性疲劳和传递性疲劳。糖原储备减少但未耗尽。体内三磷酸腺苷浓度降低,但在体外恢复。体外休息期间和刺激期间膈肌耗氧量均降低。结果表明,内毒素血症休克以时间依赖性方式导致膈肌疲劳,体外存在神经或神经肌肉传递受损,且休克膈肌耗氧量受损与高能磷酸储存减少有关。