Khan Mustafa H, Li Zhaozhu, Wang James H-C
Musculoskeletal Research Center, Department of Orthopaedic Surgery, University of Pittsburgh Medical Center, 210 Lothrop Street, Pittsburgh, PA 15213, USA.
Clin J Sport Med. 2005 Jan;15(1):27-33. doi: 10.1097/00042752-200501000-00006.
To determine whether repeated exposure of rabbit patellar tendon to prostaglandin-E(2) leads to degenerative changes in the tendon.
Laboratory animal study.
Intratendinous changes including cellularity, matrix organization, collagen fibril packing, and diameter.
Skeletally mature New Zealand White rabbits (n = 10) were transcutaneously injected in the midsubstance of the patellar tendon with prostaglandin-E(2) (PGE(2); 50 ng or 500 ng). The contralateral tendons were used as 3 different controls (no injection, saline injection, and needlestick only). The injection was repeated once a week for 4 weeks, and the rabbits were killed 1 week after the last injection. The patellar tendons were harvested and examined using hematoxylin and eosin staining and transmission electron microscopy.
Compared with the control groups, tendons exposed to PGE(2) by injection showed focal areas of hypercellularity, loss of normal tissue architecture, and focal areas of tendon disorganization and degeneration. Tendons injected with PGE(2) exhibited loosely organized collagen fibrils and had thinner collagen fibril diameter compared with control tendons (P < 0.005). Tendons injected with 500 ng PGE(2) appeared to be more disorganized and degenerated than those injected with 50 ng PGE(2).
Repeated exposure of the tendon to PGE(2) leads to degenerative changes within the tendon.
It is known that human tendon fibroblasts produce PGE(2) in vitro and in vivo in response to repetitive mechanical loading. This study demonstrates that repetitive exposure of the tendon to PGE(2) can result in degenerative changes within the tendon. Therefore, PGE(2) produced by tendon fibroblasts in response to repetitive mechanical loading in vivo might contribute to the development of exercise-induced tendinopathy.
确定兔髌腱反复暴露于前列腺素 - E(2) 是否会导致腱的退行性改变。
实验动物研究。
腱内变化,包括细胞密度、基质组织、胶原纤维排列及直径。
选用骨骼成熟的新西兰白兔(n = 10),经皮在髌腱中部注射前列腺素 - E(2)(PGE(2);50 ng 或 500 ng)。对侧腱用作 3 种不同对照(不注射、注射生理盐水及仅针刺)。每周注射 1 次,共 4 周,最后 1 次注射后 1 周处死兔子。取出髌腱,采用苏木精 - 伊红染色及透射电子显微镜检查。
与对照组相比,注射 PGE(2) 的腱出现细胞增多的局灶区域、正常组织结构丧失以及腱组织紊乱和退变的局灶区域。注射 PGE(2) 的腱胶原纤维排列松散,与对照腱相比胶原纤维直径更细(P < 0.005)。注射 500 ng PGE(2) 的腱比注射 50 ng PGE(2) 的腱紊乱和退变更明显。
腱反复暴露于 PGE(2) 会导致腱内发生退行性改变。
已知人体肌腱成纤维细胞在体外和体内对重复性机械负荷会产生 PGE(2)。本研究表明,腱反复暴露于 PGE(2) 可导致腱内发生退行性改变。因此,体内肌腱成纤维细胞对重复性机械负荷产生的 PGE(2) 可能促成运动性肌腱病的发展。