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动物模型和人类中的呼吸肌损伤。

Respiratory muscle injury in animal models and humans.

作者信息

Reid W D, MacGowan N A

机构信息

School of Rehabilitation Sciences, University of British Columbia, Vancouver, Canada.

出版信息

Mol Cell Biochem. 1998 Feb;179(1-2):63-80. doi: 10.1023/a:1006803703128.

Abstract

Respiratory muscle injury may result from excessive loading due to a decrease in respiratory muscle strength, an increase in the work of breathing, or an increase in the rate of ventilation. Other conditions such as hypoxemia, hypercapnia, aging, decreased nutrition, and immobilization may potentiate respiratory muscle injury. Respiratory muscle injury has been shown in animal models using direct muscle or phrenic nerve stimulation, acute inspiratory resistive loading, tracheal banding, corticosteroids, phrenic nerve section, and the mdx mouse. Although numerous examples of diaphragm injury have been shown in animal models, evidence in humans is sparse. Potential mechanisms which may contribute to respiratory muscle injury include high levels of intracellular calcium-activated degradative enzymes, non-uniformity of stresses and strains, plasma membrane disruptions, and activation of the inflammatory process.

摘要

呼吸肌损伤可能源于呼吸肌力量下降、呼吸功增加或通气速率增加导致的负荷过重。其他情况,如低氧血症、高碳酸血症、衰老、营养状况下降和制动,可能会加重呼吸肌损伤。在动物模型中,通过直接肌肉或膈神经刺激、急性吸气阻力负荷、气管结扎、皮质类固醇、膈神经切断和mdx小鼠等方法已证实存在呼吸肌损伤。尽管在动物模型中已展示了许多膈肌损伤的例子,但人类方面的证据却很少。可能导致呼吸肌损伤的潜在机制包括细胞内钙激活降解酶水平升高、应力和应变不均匀性、质膜破坏以及炎症过程的激活。

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