Department of Biomedical Engineering, Faculty of Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
Department of Rheumatology, Assistance Publique - Hôpitaux de Paris (AP-HP), Inserm UMRS_938, Sorbonne Université, Saint-Antoine Hospital, Paris, France.
Osteoarthritis Cartilage. 2021 May;29(5):643-653. doi: 10.1016/j.joca.2021.02.005. Epub 2021 Feb 17.
Osteoarthritis (OA) poses a major health and economic burden worldwide due to an increasing number of patients and the unavailability of disease-modifying drugs. In this review, the latest understanding of the involvement of the cholinergic system in joint homeostasis and OA will be outlined. First of all, the current evidence on the presence of the cholinergic system in the normal and OA joint will be described. Cholinergic innervation as well as the non-neuronal cholinergic system are detected. In a variety of inflammatory diseases, the classic cholinergic anti-inflammatory pathway lately received a lot of attention as via this pathway cholinergic agonists can reduce inflammation. The role of this cholinergic anti-inflammatory pathway in the context of OA will be discussed. Activation of this pathway improved the progression of the disease. Secondly, chondrocyte hypertrophy plays a pivotal role in osteophyte formation and OA development; the impact of the cholinergic system on hypertrophic chondroblasts and endochondral ossification will be evaluated. Cholinergic stimulation increased chondrocyte proliferation, delayed chondrocyte differentiation and caused early mineralisation. Moreover, acetylcholinesterase and butyrylcholinesterase affect the endochondral ossification via an acetylcholine-independent pathway. Thirdly, subchondral bone is critical for cartilage homeostasis and metabolism; the cholinergic system in subchondral bone homeostasis and disorders will be explored. An increase in osteoblast proliferation and osteoclast apoptosis is observed. Lastly, current therapeutic strategies for OA are limited to symptom relief; here the impact of smoking on disease progression and the potential of acetylcholinesterase inhibitors as candidate disease-modifying drug for OA will be discussed.
骨关节炎(OA)由于患者数量不断增加和缺乏疾病修饰药物,在全球范围内造成了重大的健康和经济负担。在这篇综述中,将概述胆碱能系统在关节稳态和 OA 中最新的参与机制。首先,将描述正常关节和 OA 关节中胆碱能系统的现有证据。检测到胆碱能神经支配和非神经元胆碱能系统。在各种炎症性疾病中,经典的胆碱能抗炎途径最近受到了很多关注,因为通过这条途径,胆碱能激动剂可以减轻炎症。将讨论该胆碱能抗炎途径在 OA 中的作用。该途径的激活改善了疾病的进展。其次,软骨细胞肥大在骨赘形成和 OA 发展中起关键作用;将评估胆碱能系统对肥大软骨细胞和成骨作用的影响。胆碱能刺激增加软骨细胞增殖,延迟软骨细胞分化并导致早期矿化。此外,乙酰胆碱酯酶和丁酰胆碱酯酶通过非乙酰胆碱依赖途径影响成骨作用。第三,软骨下骨对软骨稳态和代谢至关重要;将探讨软骨下骨稳态和疾病中的胆碱能系统。观察到成骨细胞增殖增加和破骨细胞凋亡。最后,OA 的当前治疗策略仅限于缓解症状;这里将讨论吸烟对疾病进展的影响以及乙酰胆碱酯酶抑制剂作为 OA 候选疾病修饰药物的潜力。