Schlenker E H, Burbach J A
Department of Physiology and Pharmacology, University of South Dakota School of Medicine, Vermillion 57069.
Lung. 1990;168(3):125-36. doi: 10.1007/BF02719684.
The BIO 14.6 dystrophic hamster has been used extensively over the past 30 years as an animal model in which to study the mechanisms responsible for the development of cardiomyopathy and skeletal muscle dysfunction associated with muscular dystrophy. More recently, structural and functional aspects of the respiratory system of this animal model have been investigated. This review summarizes our current knowledge of ventilation, lung morphometry and mechanics, the structure and function of the diaphragm, tracheal and pulmonary vascular smooth muscle, and pulmonary macrophages in the BIO 14.6 dystrophic hamster. We conclude that many aspects of the structure and function of the respiratory system of this hamster warrant further investigation, including the development of alveolar hypoventilation, the causes of pulmonary vascular hyporeactivity, and the potential contribution of abnormal pulmonary macrophages to the pathogenesis of life-threatening respiratory disease in muscular dystrophy.
在过去30年里,BIO 14.6营养不良性仓鼠被广泛用作动物模型,用于研究与肌肉萎缩症相关的心肌病和骨骼肌功能障碍的发病机制。最近,人们对该动物模型呼吸系统的结构和功能方面进行了研究。这篇综述总结了我们目前对BIO 14.6营养不良性仓鼠的通气、肺形态学和力学、膈肌、气管和肺血管平滑肌以及肺巨噬细胞的结构和功能的认识。我们得出结论,该仓鼠呼吸系统结构和功能的许多方面值得进一步研究,包括肺泡通气不足的发展、肺血管反应性降低的原因,以及异常肺巨噬细胞对肌肉萎缩症中危及生命的呼吸系统疾病发病机制的潜在影响。