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首页> 外文期刊>Journal of bone and mineral metabolism >Incadronate disodium inhibits joint destruction and periarticular bone loss only in the early phase of rat adjuvant-induced arthritis.
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Incadronate disodium inhibits joint destruction and periarticular bone loss only in the early phase of rat adjuvant-induced arthritis.

机译:仅仅在大鼠佐剂诱发的关节炎的早期阶段,中钙二钠才抑制关节破坏和关节周围骨丢失。

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摘要

Destruction of articular cartilage and subchon-dral bone loss in the affected joints of rat adjuvant arthritis have never been quantified histologically. This study aimed to evaluate the effect of incadronate disodium on joint destruction and periarticular bone loss, using histomorphometric measurements. Seven-week-old female Lewis rats were injected with 0.1 mg of heat-killed Mycobacterium butyricum into the tail base. Immediately after sensitization, vehicle, or incadronate at 10 or 100 microg/kg per day, was administered subcutaneously, three times per week. Hind-paw volume was measured weekly and the animals were killed at 2, 4, 6, and 10 weeks after sensitization. After taking X-rays, decalcified sagittal sections of the ankle joint were prepared and stained with toluidine blue and tartarate-resistant acid phosphatase. Articular cartilage destruction and subchondral bone loss were evaluated histomorphometrically. At 2 weeks after sensitization, no radiographic or histologic changes were observed. However, at 4 weeks, severe articular cartilage destruction and subchondral bone loss were found in the arthritic control group, while these changes were inhibited dose-dependently by incadronate treatment. At 6 and 10 weeks, both the destructive changes and the bone loss had further progressed, and they were not inhibited by incadronate treatment. Incadronate dose-dependently inhibited articular cartilage destruction and subchondral bone loss at 4 weeks after sensitization in this adjuvant arthritis model. However, the suppressive effects of incadronate did not continue until 6 and 10 weeks.
机译:尚未从组织学上量化大鼠佐剂关节炎的受影响关节中关节软骨的破坏和软骨下骨丢失。这项研究的目的是使用组织形态计量学来评估钙二钠对关节破坏和关节周围骨丢失的影响。七周大的雌性Lewis大鼠被注入0.1 mg的热杀死的丁酸分枝杆菌到尾巴基部。致敏后,每周皮下注射媒介物或钙盐,每天10或100 microg / kg。每周测量后爪体积,并在致敏后2、4、6和10周处死动物。拍摄X射线后,准备踝关节脱钙的矢状切面,并用甲苯胺蓝和耐酒石酸的酸性磷酸酶染色。用组织形态计量学评价关节软骨破坏和软骨下骨丢失。致敏后2周,未观察到影像学或组织学改变。然而,在第4周,在关节炎对照组中发现了严重的关节软骨破坏和软骨下骨丢失,而这些变化被钙盐酸盐治疗剂量依赖性地抑制。在第6周和第10周,破坏性变化和骨丢失均进一步发展,并且不受钙盐酸盐治疗的抑制。在这种佐剂性关节炎模型中,致敏后第4周,学院酸剂量依赖性地抑制关节软骨破坏和软骨下骨丢失。但是,直到6周和10周时,钙制高铁的抑制作用才持续。

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