Sanchez J, Derenne J P, Debesse B, Riquet M, Monod H
Bull Eur Physiopathol Respir. 1982 Nov-Dec;18(6):901-14.
Histochemical muscle fibre composition was studied in biopsies from the diaphragm, the external and internal intercostal muscles in the fifth intercostal space and horizontal and vertical parts of the serratus in 8 subjects with normal lung function and in 18 patients with abnormal lung function (6 restrictive and 12 obstructive). Muscle fibres were classified as type I (slow twitch) or type II (fast twitch) on the basis of their myofibrillar ATPase pH lability. All the muscles studied showed a mosaic pattern with the two fibre types. In every respiratory muscle, the percentage of type I fibres was higher than 50%. There was no significant difference between the three groups (normal, restrictive and obstructive) for each of the six muscles studied. The fibre diameters were similar for all types and muscles (range of means: 41-63 micron), except for the diaphragm in which the diameters of type I and type II fibres were significantly higher in the normal subjects as compared to the obstructive and restrictive patients. Moreover, there was a significant linear correlation between the diameter of the diaphragmatic fibres and vital capacity and FEV1. A low "atrophy factor" was found for each muscle studied with a large intra-individual variation. The results support the idea that the increased respiratory loading due to disease do not hypertrophy the respiratory muscles and suggest that the effect of the disease on the respiratory muscles is more related to the increased mechanical impedance of the respiratory system rather than to the changes in thoracic configuration.
对8名肺功能正常的受试者以及18名肺功能异常的患者(6名限制性通气障碍患者和12名阻塞性通气障碍患者)的膈肌、第五肋间间隙的肋间外肌和肋间内肌、以及锯肌的水平部和垂直部活检组织进行了组织化学肌纤维组成研究。根据肌原纤维ATP酶pH稳定性,将肌纤维分为I型(慢肌纤维)或II型(快肌纤维)。所有研究的肌肉均呈现出两种纤维类型的镶嵌模式。在每块呼吸肌中,I型纤维的百分比均高于50%。在所研究的六块肌肉中,三组(正常、限制性通气障碍和阻塞性通气障碍)之间均无显著差异。除膈肌外,所有类型和肌肉的纤维直径相似(平均范围:41 - 63微米),在膈肌中,与阻塞性通气障碍和限制性通气障碍患者相比,正常受试者的I型和II型纤维直径显著更高。此外,膈肌纤维直径与肺活量和第一秒用力呼气量之间存在显著的线性相关性。在所研究的每块肌肉中均发现了较低的“萎缩因子”,个体内差异较大。结果支持这样的观点,即疾病导致的呼吸负荷增加并不会使呼吸肌肥大,并且表明疾病对呼吸肌的影响更多地与呼吸系统机械阻抗增加有关,而非与胸廓形态的变化有关。