Beverly M, Mellon S, Kennedy J A, Murray D W
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Botnar Research Centre, Nuffield Orthopaedic Centre, Oxford, UK.
Bone Joint Res. 2018 Sep 15;7(8):511-516. doi: 10.1302/2046-3758.78.BJR-2017-0343.R2. eCollection 2018 Aug.
We studied subchondral intraosseous pressure (IOP) in an animal model during loading, and with vascular occlusion. We explored bone compartmentalization by saline injection.
Needles were placed in the femoral condyle and proximal tibia of five anaesthetized rabbits and connected to pressure recorders. The limb was loaded with and without proximal vascular occlusion. An additional subject had simultaneous triple recordings at the femoral head, femoral condyle and proximal tibia. In a further subject, saline injections at three sites were carried out in turn.
Loading alone caused a rise in subchondral IOP from 11.7 mmHg (sd 7.1) to 17.9 mmHg (sd 8.1; p < 0.0002). During arterial occlusion, IOP fell to 5.3 mmHg (sd 4.1), then with loading there was a small rise to 7.6 mmHg (sd 4.5; p < 0.002). During venous occlusion, IOP rose to 20.2 mmHg (sd 5.8), and with loading there was a further rise to 26.3 mmHg (sd 6.3; p < 0.003). The effects were present at three different sites along the limb simultaneously. Saline injections showed pressure transmitted throughout the length of the femur but not across the knee joint.
This is the first study to report changes in IOP during loading and with combinations of vascular occlusion and loading. Intraosseous pressure is not a constant. It is reduced during proximal arterial occlusion and increased with proximal venous occlusion. Whatever the perfusion state, load is transferred partly by hydraulic pressure. We propose that joints act as hydraulic pressure barriers. An understanding of subchondral physiology may be important in understanding osteoarthritis and other bone diseases.: M. Beverly, S. Mellon, J. A. Kennedy, D. W. Murray. Intraosseous pressure during loading and with vascular occlusion in an animal model. 2018;7:511-516. DOI: 10.1302/2046-3758.78.BJR-2017-0343.R2.
我们在动物模型中研究了加载过程中以及血管闭塞时的软骨下骨内压(IOP)。我们通过注射生理盐水探索了骨的分隔情况。
将针置于五只麻醉兔的股骨髁和胫骨近端,并连接到压力记录仪。在有或没有近端血管闭塞的情况下对肢体进行加载。另一只实验对象在股骨头、股骨髁和胫骨近端同时进行三重记录。在另一只实验对象中,依次在三个部位进行生理盐水注射。
单独加载导致软骨下骨内压从11.7 mmHg(标准差7.1)升至17.9 mmHg(标准差8.1;p < 0.0002)。在动脉闭塞期间,骨内压降至5.3 mmHg(标准差4.1),然后加载时略有上升至7.6 mmHg(标准差4.5;p < 0.002)。在静脉闭塞期间,骨内压升至20.2 mmHg(标准差5.8),加载时进一步升至26.3 mmHg(标准差6.3;p < 0.003)。这些效应同时出现在肢体的三个不同部位。生理盐水注射显示压力沿股骨全长传递,但不穿过膝关节。
这是第一项报告加载过程中以及血管闭塞与加载组合时骨内压变化的研究。骨内压不是恒定的。在近端动脉闭塞时降低,在近端静脉闭塞时升高。无论灌注状态如何,负荷部分通过液压传递。我们认为关节起到液压屏障的作用。了解软骨下生理学对于理解骨关节炎和其他骨疾病可能很重要。:M. 贝弗利、S. 梅隆、J. A. 肯尼迪、D. W. 默里。动物模型中加载及血管闭塞时的骨内压。2018;7:511 - 516。DOI:10.1302/2046 - 3758.78.BJR - 2017 - 0343.R2。