Effects of Each Phase of Anterior Cruciate Ligament Reconstruction Surgery on Joint Contracture in Rats
Effects of Each Phase of Anterior Cruciate Ligament Reconstruction Surgery on Joint Contracture in Rats
复制标题
前交叉韧带重建手术各阶段对大鼠关节挛缩的影响
DOI:
10.1080/08941939.2021.1985193
复制
发表时间:
2021
影响因子:
1.9
通讯作者:
Yamaoka Kaoru
中科院分区:
文献类型:
--
作者:
Kaneguchi Akinori;Ozawa Junya;Minamimoto Kengo;Yamaoka Kaoru
BackgroundAlthough anterior cruciate ligament reconstruction surgery is known to cause joint contracture, the mechanisms of this process are unknown. We aimed to assess the effects of transection of this ligament and each phase of reconstruction surgery on contracture formation.Materials and methodsRats were divided into groups according to treatment received: sham (arthrotomy), ligament transection, ligament transection plus bone drilling, and ligament reconstruction. Surgery was performed on the right knee. Untreated left knees in the sham group were used as controls.ResultsAt 7 and 28 d post-surgery, range of motion before myotomy, mainly representing myogenic contracture, was restricted in the sham and ligament transection groups, and more so in the bone drilling and reconstruction groups. Restricted range of motion after myotomy, representing arthrogenic contracture, was detected at both timepoints in the bone drilling and reconstruction groups, but not in the sham or ligament transection groups. At 3 d post-surgery, although a large blood clot was observed in all three treatment groups, only the bone drilling and reconstruction groups showed significant joint swelling. At 7 d post-surgery, inflammatory-cell infiltration into the joint capsule was most apparent in the bone drilling and reconstruction groups, and joint capsule fibrosis was also most apparent in these groups at 7 and 28 d post-surgery.ConclusionsOur results suggest that (1) myogenic contracture after anterior cruciate ligament reconstruction is caused by arthrotomy and aggravated by bone drilling, and (2) arthrogenic contracture is mostly due to bone drilling, which triggers an inflammation–fibrosis cascade.
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DOI:
10.1210/jcem.83.6.4848
发表时间:
1998
期刊:
The Journal of clinical endocrinology and metabolism.
影响因子:
--
作者:
Cheleuitte,D;Mizuno,S;Glowacki,J
通讯作者:
Glowacki,J
DOI:
--
发表时间:
2001
期刊:
影响因子:
--
作者:
P. Millett;T. Wickiewicz;R. Warren
通讯作者:
R. Warren
影响因子:
1.1
作者:
Ben K. Graf;Judson W Ott;Richard H. Lange;James S. Keene
通讯作者:
James S. Keene
影响因子:
5.3
作者:
Austin, John C.;Phornphutkul, Chanakarn;Wojtys, Edward M.
通讯作者:
Wojtys, Edward M.
影响因子:
4.1
作者:
Eckenrode, Brian J.;Carey, James L.;Zgonis, Miltiadis H.
通讯作者:
Zgonis, Miltiadis H.