分解代谢
胶原酶
炎症
关节炎
医学
蛋白多糖
细胞外基质
软骨
机制(生物学)
基质金属蛋白酶
细胞生物学
糖胺聚糖
关节软骨
功能(生物学)
酶
生物物理学
免疫学
生物化学
病理
骨关节炎
生物
内科学
解剖
新陈代谢
哲学
替代医学
认识论
标识
DOI:10.7326/0003-4819-88-6-821
摘要
Erosion of joint surfaces in arthritic conditions is always associated with the degradation of the two principal matrix macromolecules of cartilage, proteoglycan and collagen. The major enzymes thought to be involved in articular catabolism have now been isolated, purified, and their properties studied, but precise spatial and temporal activities are still imperfectly understood. We are beginning to understand some aspects of cellular function in the control of catabolic enzyme function. Recent studies on molecular, cellular, and tissue mechanisms in this process are discussed here. Of particular interest is a possible natural control mechanism involving a recently discovered inhibitor of collagenase. A newly developed pharmacologic method of inflammation control utilizes the properties of liposomes in the closed environment of the joint cavity. Very low doses of modified steroids encapsulated within liposomes are capable of substantially reducing inflammation in experimentally arthritic animals and may be applicable to man.
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