Aoyagi T, Wada T, Yamamoto K, Kojima F, Nagai M, Umezawa H
J Pharmacobiodyn. 1984 May;7(5):312-21. doi: 10.1248/bpb1978.7.312.
The present study was undertaken to compare the peculiarity of enzymatic changes in dystrophic hamsters and mice. Various enzymatic activities in muscle, bone, heart, spleen, liver and kidney were measured. The enzymes tested include 7 aminopeptidases, 5 endopeptidases, 3 glycosidases, creatine kinase, phosphatase and esterase. In dystrophic mice, the enzymatic changes were chiefly confined to muscle and bone. In dystrophic hamsters, on the other hand, extensive and pronounced changes in enzymatic activities were seen not only in skeletal muscle but also in bone, heart muscle, spleen, liver and kidney. Furthermore, resemblance of pattern of enzymatic changes was seen among several organs including skeletal muscle, heart muscle, bone and spleen in the hamster model. Comparing the enzymatic changes in these two models, dystrophic mouse may be regarded as more specific a model for musculoskeletal diseases. Dystrophic hamster may be related more to multiorgan diseases possibly associated with immunological or other systemic diseases. These models may represent two different disease categories, respectively.
本研究旨在比较营养不良的仓鼠和小鼠体内酶变化的特点。测定了肌肉、骨骼、心脏、脾脏、肝脏和肾脏中的各种酶活性。所检测的酶包括7种氨基肽酶、5种内肽酶、3种糖苷酶、肌酸激酶、磷酸酶和酯酶。在营养不良的小鼠中,酶变化主要局限于肌肉和骨骼。另一方面,在营养不良的仓鼠中,不仅在骨骼肌中,而且在骨骼、心肌、脾脏、肝脏和肾脏中都观察到酶活性广泛而明显的变化。此外,在仓鼠模型中,包括骨骼肌、心肌、骨骼和脾脏在内的几个器官之间观察到酶变化模式的相似性。比较这两种模型中的酶变化,营养不良的小鼠可能被视为肌肉骨骼疾病更具特异性的模型。营养不良的仓鼠可能与可能与免疫或其他全身性疾病相关的多器官疾病关系更大。这些模型可能分别代表两种不同的疾病类别。