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首页> 外文期刊>Journal of orthopaedic research >Attenuation of cartilage degeneration by calcitonin gene-related paptide receptor antagonist via inhibition of subchondral bone sclerosis in osteoarthritis mice
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Attenuation of cartilage degeneration by calcitonin gene-related paptide receptor antagonist via inhibition of subchondral bone sclerosis in osteoarthritis mice

机译:降钙素基因相关的八肽受体拮抗剂通过抑制骨关节炎小鼠的软骨下骨硬化来减轻软骨变性

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摘要

Osteoarthritis (OA) is a progressive joint disorder which affects cartilage and subchondral bone. Calcitonin gene-related peptide (CGRP) plays a role in bone metabolism. The purpose of this study is to examine the therapeutic effect of the blocking CGRP on OA progression in mice by inhibition of subchondral bone sclerosis. OA was induced by the resection of the medial meniscotibial ligament of the knee in C57/BL6 mice. An intraperitoneal injection of the CGRP receptor antagonist (BIBN4096) was administered after OA surgery. At 1, 4, and 8 weeks after injection, histological analysis were performed. In vitro, the effect of CGRP and BIBN4096 on osteogenesis and osteoclastogenesis was analyzed. BIBN4096 could prevent cartilage degeneration and subchondral bone sclerosis. The OARSI score in the BIBN4096 group was significantly lower than that in the control. In vitro, CGRP up regulated osteocalcin expression, but its expression was down regulated by BIBN4096. CGRP inhibited osteoclastogenesis of raw 267.4 cells, but its effect was reduced by the addition of BIBN4096.The current study showed that subchondral bone sclerosis and increasing expression of CGRP occurs in the early phase of OA in relation to cartilage degeneration, and that BIBN4096 could effectively attenuate OA progression. (c) 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1177-1184, 2016.
机译:骨关节炎(OA)是一种进行性关节疾病,会影响软骨和软骨下骨。降钙素基因相关肽(CGRP)在骨代谢中起作用。这项研究的目的是通过抑制软骨下骨硬化来检查阻断CGRP对小鼠OA进展的治疗作用。在C57 / BL6小鼠中,膝关节内侧半月板韧带切除术诱发了OA。 OA手术后腹膜内注射CGRP受体拮抗剂(BIBN4096)。注射后第1、4和8周,进行组织学分析。在体外,分析了CGRP和BIBN4096对成骨和破骨细胞的作用。 BIBN4096可预防软骨变性和软骨下骨硬化。 BIBN4096组的OARSI得分显着低于对照组。在体外,CGRP上调了骨钙素的表达,但其表达被BIBN4096下调。 CGRP抑制了原始的267.4细胞的破骨细胞生成,但加入BIBN4096降低了其作用。目前的研究表明,软骨下骨硬化和CGRP表达的增加与软骨退变有关,并且在OA的早期阶段发生,而BIBN4096可以有效地减弱OA进展。 (c)2015骨科研究学会。由Wiley Periodicals,Inc.出版J Orthop Res 34:1177-1184,2016。

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