Meyer P, Burkhardt H, Palombo-Kinne E, Gründer W, Bräuer R, Stiller K J, Kalden J R, Becker W, Kinne R W
University of Göttingen, Germany.
Arthritis Rheum. 2000 Feb;43(2):298-310. doi: 10.1002/1529-0131(200002)43:2<298::AID-ANR9>3.0.CO;2-G.
To assess the involvement of the contralateral knee joint in monarticular antigen-induced arthritis (AIA) by scintigraphy with the cationic (pI >10), 123I-labeled, serine proteinase inhibitor antileukoproteinase (123I-ALP) and to compare the scintigraphic findings with those of radiography and high-resolution ex vivo magnetic resonance imaging (MRI).
Lewis rats with chronic AIA were examined 2.5 months following arthritis induction (injection of 500 microg of methylated bovine serum albumin/saline into the ipsilateral [arthritic] knee joint and injection of phosphate buffered saline into the contralateral knee joint following systemic immunization). 123I-ALP was injected intravenously into normal rats (n = 4) or rats with AIA (n = 6). The ipsilateral and contralateral knee joints and both ankles were examined by scintigraphy and radiography. Joint cartilage was examined by high-resolution ex vivo MRI, histopathology, and measurement of tissue radioactivity.
ALP accumulation (typically observed in normal articular cartilage) was lost in both the ipsilateral and the contralateral knee joints, but not in the clinically unaffected ankles of rats with AIA. In both knee joints, 123I-ALP target:background ratios and cartilage radioactivity correlated negatively with the loss of toluidine blue staining in cartilage, which documents the depletion of charged matrix molecules. Findings of histopathology confirmed mild alterations in the ipsilateral knee joint and even milder alterations in the contralateral knee joint, while the ankles were normal. Radiography and high-resolution ex vivo MRI failed to detect abnormalities in the contralateral knee joint.
Loss of ALP accumulation appears to document proteoglycan depletion, even in the microscopically altered cartilage of the contralateral knee joint in AIA. These findings underscore the high sensitivity of 123I-ALP for in vivo detection of biochemical cartilage alterations in arthritis, and furthermore, question the use of the contralateral knee joint as a normal control in AIA.
通过使用阳离子(pI >10)、123I标记的丝氨酸蛋白酶抑制剂抗白细胞蛋白酶(123I-ALP)进行闪烁扫描,评估单关节抗原诱导性关节炎(AIA)中对侧膝关节的受累情况,并将闪烁扫描结果与放射摄影和高分辨率离体磁共振成像(MRI)结果进行比较。
对诱导关节炎2.5个月后的慢性AIA刘易斯大鼠进行检查(全身免疫后,向同侧[患关节炎的]膝关节注射500微克甲基化牛血清白蛋白/生理盐水,向对侧膝关节注射磷酸盐缓冲盐水)。将123I-ALP静脉注射到正常大鼠(n = 4)或AIA大鼠(n = 6)体内。通过闪烁扫描和放射摄影检查同侧和对侧膝关节以及双侧踝关节。通过高分辨率离体MRI、组织病理学和组织放射性测量来检查关节软骨。
在同侧和对侧膝关节中均未观察到正常关节软骨中典型的ALP积累,但在AIA大鼠临床未受累的踝关节中观察到了。在两个膝关节中,123I-ALP的靶标:本底比值和软骨放射性与软骨中甲苯胺蓝染色的丧失呈负相关,这表明带电荷的基质分子减少。组织病理学结果证实同侧膝关节有轻度改变,对侧膝关节改变更轻,而踝关节正常。放射摄影和高分辨率离体MRI未能检测到对侧膝关节的异常。
即使在AIA对侧膝关节微观改变的软骨中,ALP积累的丧失似乎也表明蛋白聚糖减少。这些发现强调了123I-ALP在体内检测关节炎中软骨生化改变的高敏感性,此外,还对在AIA中使用对侧膝关节作为正常对照提出了质疑。