Time course and localization of nerve growth factor expression and sensory nerve growth during progression of knee osteoarthritis in rats

神经生长因子 降钙素基因相关肽 医学 骨关节炎 降钙素 内科学 内分泌学 感觉神经 感觉系统 病理 神经肽 受体 生物 神经科学 替代医学
作者
Koji Aso,David A. Walsh,Hiroyuki Wada,Masashi Izumi,H. Tomitori,K. Fujii,Masahiko Ikeuchi
出处
期刊:Osteoarthritis and Cartilage [Elsevier]
卷期号:30 (10): 1344-1355 被引量:4
标识
DOI:10.1016/j.joca.2022.07.003
摘要

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.
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