Aso K, Walsh D A, Wada H, Izumi M, Tomitori H, Fujii K, Ikeuchi M
Department of Orthopedic Surgery, Kochi Medical School, Kochi University, 185-1 Oko-cho Kohasu, Nankoku 783-8505, Japan.
Pain Centre Versus Arthritis & NIHR Nottingham Biomedical Research Centre, University of Nottingham, Nottingham, NG5 1PB, UK.
Osteoarthritis Cartilage. 2022 Oct;30(10):1344-1355. doi: 10.1016/j.joca.2022.07.003. Epub 2022 Jul 14.
Nerve growth factor (NGF) and sensory nerves are key factors in established osteoarthritis (OA) knee pain. We investigated the time course of NGF expression and sensory nerve growth across early and late stages of OA progression in rat knees.
Knee OA was induced by medial meniscectomy in rats. OA histopathology, NGF expression, and calcitonin gene-related peptide immunoreactive (CGRP-IR) nerves were quantified pre-surgery and post-surgery at weeks 1, 2, 4 and 6. Pain-related behavior was evaluated using dynamic weight distribution and mechanical sensitivity of the hind paw.
NGF expression in chondrocytes increased from week 1 and remained elevated until the advanced stage. In synovium, NGF expression increased only in early stages, whereas in osteochondral channels and bone marrow, NGF expression increased in the later stages of OA progression. CGRP-IR nerve density in suprapatellar pouch peaked at week 4 and decreased at week 6, whereas in osteochondral channels and bone marrow, CGRP-IR innervation increased through week 6. Percent ipsilateral weight-bearing decreased throughout the OA time course, whereas reduced paw withdrawal thresholds were observed only in later stages.
During progression of knee OA, time-dependent alterations of NGF expression and CGRP-IR sensory innervation are knee tissue specific. NGF expression increased in early stages and decreased in advanced stage in the synovium but continued to increase in osteochondral channels and bone marrow. Increases in CGRP- IR sensory innervation followed increases in NGF expression, implicating that NGF is a key driver of articular nerve growth associated with OA pain.
神经生长因子(NGF)和感觉神经是已确诊的骨关节炎(OA)膝关节疼痛的关键因素。我们研究了大鼠膝关节OA进展早期和晚期NGF表达及感觉神经生长的时间进程。
通过内侧半月板切除术诱导大鼠膝关节OA。在手术前以及手术后第1、2、4和6周对OA组织病理学、NGF表达和降钙素基因相关肽免疫反应性(CGRP-IR)神经进行定量分析。使用后爪的动态重量分布和机械敏感性评估疼痛相关行为。
软骨细胞中NGF表达从第1周开始增加,并一直保持升高直至晚期。在滑膜中,NGF表达仅在早期增加,而在骨软骨通道和骨髓中,NGF表达在OA进展的后期增加。髌上囊的CGRP-IR神经密度在第4周达到峰值,并在第6周下降,而在骨软骨通道和骨髓中,CGRP-IR神经支配在第6周时持续增加。在整个OA病程中同侧负重百分比下降,而仅在后期观察到后爪退缩阈值降低。
在膝关节OA进展过程中,NGF表达和CGRP-IR感觉神经支配的时间依赖性改变具有膝关节组织特异性。滑膜中NGF表达在早期增加而在晚期减少,但在骨软骨通道和骨髓中持续增加。CGRP-IR感觉神经支配的增加跟随NGF表达增加,这表明NGF是与OA疼痛相关的关节神经生长的关键驱动因素。