Criswell David S, Shanely R Andrew, Betters Jenna J, McKenzie Michael J, Sellman Jeff E, Van Gammeren Darin L, Powers Scott K
Department of Exercise and Sport Sciences, Center for Exercise Science, University of Florida, Gainesville, FL 32611, USA.
Chest. 2003 Dec;124(6):2302-8. doi: 10.1378/chest.124.6.2302.
Unloading the diaphragm, via mechanical ventilation (MV), results in significant diaphragmatic atrophy, contractile dysfunction, and oxidative stress in young adult animals. Since aging increases skeletal muscle susceptibility to atrophy and injury, we tested the hypothesis that MV-induced diaphragmatic contractile dysfunction would be exacerbated in aging rats.
Fisher 344/Brown Norway hybrid rats (4 months old [young] and 30 months old [old]) were assigned to either control or MV groups. MV rats were anesthetized, tracheostomized, and ventilated with 21% O(2) for 12 h. Arterial BP, pH, and blood gas homeostasis were maintained in the MV animals throughout the experimental period. Animals in the control group were acutely anesthetized, and the diaphragms were immediately removed. Muscle strips from the mid-costal diaphragm were removed from each experimental animal, and contractile properties were studied in vitro.
Compared to young control animals, aging (old control animals) was associated with a 13% decrease in maximal isometric tension (24.5 N/cm(2) vs 21.3 N/cm(2)). Although, MV induced similar relative losses (24%) in diaphragmatic isometric tension in both young and old animals receiving MV, the combined effects of aging and MV resulted in a 34% decrement in diaphragmatic isometric tension compared to young control animals (24.5 N/cm(2) vs 16.1 N/cm(2)).
These data do not support the hypothesis that aging exacerbates the relative MV-induced impairment in diaphragmatic isometric tension. Nonetheless, the additive effects of aging and MV have dramatic effects on diaphragmatic force reserve. This could exacerbate weaning difficulties in older individuals receiving MV.
通过机械通气(MV)使膈肌卸载,会导致成年幼龄动物出现明显的膈肌萎缩、收缩功能障碍和氧化应激。由于衰老会增加骨骼肌对萎缩和损伤的易感性,我们检验了以下假设:MV诱导的膈肌收缩功能障碍在衰老大鼠中会加剧。
将费希尔344/布朗挪威杂交大鼠(4个月龄[幼龄]和30个月龄[老龄])分为对照组或MV组。对MV组大鼠进行麻醉、气管切开,并使用21%氧气通气12小时。在整个实验期间,维持MV组动物的动脉血压、pH值和血气平衡。对照组动物进行急性麻醉,然后立即取出膈肌。从每只实验动物的肋中膈肌处取下肌肉条,在体外研究其收缩特性。
与幼龄对照动物相比,衰老(老龄对照动物)使最大等长张力降低了13%(24.5牛/平方厘米对21.3牛/平方厘米)。虽然,MV在接受MV的幼龄和老龄动物中均导致膈肌等长张力出现相似的相对损失(24%),但衰老和MV的联合作用使膈肌等长张力相较于幼龄对照动物降低了34%(24.5牛/平方厘米对16.1牛/平方厘米)。
这些数据不支持衰老会加剧MV诱导的膈肌等长张力相对损伤这一假设。尽管如此,衰老和MV的叠加效应会对膈肌力量储备产生显著影响。这可能会加剧接受MV的老年个体的撤机困难。