Maes Karen, Testelmans Dries, Cadot Pascal, Deruisseau Keith, Powers Scott K, Decramer Marc, Gayan-Ramirez Ghislaine
Respiratory Muscle Research Unit, Laboratory of Pneumology and Respiratory Division, Katholieke Universiteit Leuven, Leuven, Belgium.
Am J Respir Crit Care Med. 2008 Dec 15;178(12):1219-26. doi: 10.1164/rccm.200702-296OC. Epub 2008 Oct 10.
Mechanical ventilation is known to induce ventilator-induced diaphragm dysfunction. Patients submitted to mechanical ventilation often receive massive doses of corticosteroids that may cause further deterioration of diaphragm function.
To examine whether the combination of 24 hours of controlled mechanical ventilation with corticosteroid administration would exacerbate ventilator-induced diaphragm dysfunction.
Rats were randomly assigned to a group submitted to 24 hours of controlled mechanical ventilation receiving an intramuscular injection of saline or 80 mg/kg methylprednisolone, a group submitted to 24 hours of spontaneous breathing receiving saline, or methylprednisolone and a control group.
The diaphragm force-frequency curve was shifted downward in the mechanical ventilation group, but this deleterious effect was prevented when corticosteroids were administered. Diaphragm cross-sectional area of type I fibers was similarly decreased in both mechanical ventilation groups while atrophy of type IIx/b fibers was attenuated after corticosteroid administration. The mechanical ventilation-induced reduction in diaphragm MyoD and myogenin protein expression was attenuated after corticosteroids. Plasma cytokine levels were unchanged while diaphragm lipid hydroperoxides were similarly increased in both mechanical ventilation groups. Diaphragmatic calpain activity was significantly increased in the mechanical ventilation group, but calpain activation was abated with corticosteroid administration. Inverse correlations were found between calpain activity and diaphragm force.
A single high dose of methylprednisolone combined with controlled mechanical ventilation protected diaphragm function from the deleterious effects of controlled mechanical ventilation. Inhibition of the calpain system is most likely the mechanism by which corticosteroids induce this protective effect.
已知机械通气会诱发呼吸机诱导的膈肌功能障碍。接受机械通气的患者常接受大剂量皮质类固醇治疗,这可能会导致膈肌功能进一步恶化。
研究24小时控制性机械通气联合皮质类固醇给药是否会加重呼吸机诱导的膈肌功能障碍。
将大鼠随机分为三组,一组接受24小时控制性机械通气并肌肉注射生理盐水或80mg/kg甲泼尼龙,一组接受24小时自主呼吸并注射生理盐水或甲泼尼龙,还有一组为对照组。
机械通气组的膈肌力-频率曲线向下移位,但给予皮质类固醇时可防止这种有害影响。两个机械通气组中I型纤维的膈肌横截面积均同样减小,而给予皮质类固醇后IIx/b型纤维的萎缩减轻。皮质类固醇给药后,机械通气诱导的膈肌MyoD和肌细胞生成素蛋白表达降低得到缓解。两组机械通气组的血浆细胞因子水平均未改变,而膈肌脂质氢过氧化物均同样增加。机械通气组的膈肌钙蛋白酶活性显著增加,但给予皮质类固醇可减轻钙蛋白酶激活。发现钙蛋白酶活性与膈肌力量呈负相关。
单次高剂量甲泼尼龙联合控制性机械通气可保护膈肌功能免受控制性机械通气的有害影响。抑制钙蛋白酶系统很可能是皮质类固醇产生这种保护作用的机制。