Reddy G K, Dhar S C
Department of Biochemistry, Central Leather Research Institute, Madras, India.
Calcif Tissue Int. 1992 Apr;50(4):320-6. doi: 10.1007/BF00301629.
The metabolic alterations in the matrix of connective tissue collagen were investigated in bone and tendon of rats with adjuvant-induced arthritis. Adjuvant arthritis was induced in rats with the immunization of Freund's adjuvant containing heat-killed Mycobacterium tuberculosis. The changes in the metabolism of collagen were studied using radioactive isotopic measurements with (3H)-proline. Tissue specimens were fractionated individually into soluble and insoluble collagens. The synthesis of collagen was examined by measuring the total collagen content and the radioactivity of (3H)-hydroxyproline in soluble collagen fraction within 24 hours after the administration of tritiated proline. The conversion of soluble to insoluble collagen was analyzed by measuring the radioactivity of (3H)-hydroxyproline in both soluble and insoluble collagens. The catabolism of soluble and insoluble collagens was studied by estimating the radioactivity of urinary (3H)-hydroxyproline 24 hours after the injection of tritiated proline. It was observed that the total collagen content and the total radioactivity of (3H)-hydroxyproline in bone and tendon were decreased significantly in adjuvant arthritic rats. The specific and total radioactivities of (3H)-hydroxyproline in soluble collagen were found to be reduced, indicating the decreased de novo synthesis of collagen during the diseased state. The conversion of soluble to insoluble collagen was impaired in tissues as evidenced by the increased content of soluble collagen in arthritic disease. In addition, an enhanced excretion of hydroxyproline was found in urine of arthritic rats, indicating the increased degradation of collagen in arthritic disease. These observations could, therefore, explain in part the changes in synthesis and degradation of collagen in bone and tendon during the development of experimentally induced adjuvant arthritis in rats.
在佐剂诱导性关节炎大鼠的骨骼和肌腱中,对结缔组织胶原蛋白基质中的代谢改变进行了研究。通过用含有热灭活结核分枝杆菌的弗氏佐剂免疫大鼠来诱导佐剂性关节炎。使用(3H)-脯氨酸的放射性同位素测量法研究胶原蛋白的代谢变化。将组织标本分别分离为可溶性胶原蛋白和不溶性胶原蛋白。通过测量给予氚化脯氨酸后24小时内可溶性胶原蛋白部分的总胶原蛋白含量和(3H)-羟脯氨酸的放射性来检测胶原蛋白的合成。通过测量可溶性和不溶性胶原蛋白中(3H)-羟脯氨酸的放射性来分析可溶性胶原蛋白向不溶性胶原蛋白的转化。通过估计注射氚化脯氨酸后24小时尿中(3H)-羟脯氨酸的放射性来研究可溶性和不溶性胶原蛋白的分解代谢。观察到佐剂性关节炎大鼠骨骼和肌腱中的总胶原蛋白含量以及(3H)-羟脯氨酸的总放射性显著降低。发现可溶性胶原蛋白中(3H)-羟脯氨酸的比放射性和总放射性均降低,表明在患病状态下胶原蛋白的从头合成减少。如在关节炎疾病中可溶性胶原蛋白含量增加所证明的,组织中可溶性胶原蛋白向不溶性胶原蛋白的转化受损。此外,在关节炎大鼠的尿液中发现羟脯氨酸排泄增加,表明关节炎疾病中胶原蛋白的降解增加。因此,这些观察结果可以部分解释在大鼠实验性诱导的佐剂性关节炎发展过程中骨骼和肌腱中胶原蛋白合成和降解的变化。