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骨关节炎的脑-关节轴:神经、生物钟及其他。

The brain-joint axis in osteoarthritis: nerves, circadian clocks and beyond.

机构信息

Rheumatology Department, Sorbonnes Universités UPMC Univ Paris 06, INSERM UMRS_938, DHU i2B, Assistance Publique-Hopitaux de Paris, Hôpital Saint-Antoine, 184 rue du Faubourg Saint-Antoine, Paris 75012, France.

Faculty of Biology, Medicine and Health, Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Oxford Road, Manchester M13 9PT, UK. University of Manchester.

出版信息

Nat Rev Rheumatol. 2016 Sep;12(9):508-16. doi: 10.1038/nrrheum.2016.93. Epub 2016 Jun 16.


DOI:10.1038/nrrheum.2016.93
PMID:27305851
Abstract

Osteoarthritis (OA) is a prevalent and debilitating joint disease for which ageing, obesity and chronic inflammation are known risk factors. The central, peripheral and autonomic nervous systems are essential in all metabolic systems, and emerging evidence suggests a role for these systems in OA. In the past few years, metabolic diseases, such as obesity or diabetes, have been linked to disruption of circadian rhythms that are tightly regulated by the nervous system, whereas inflammatory and autoimmune diseases are known to be linked to disruption of the cholinergic vagus nerve reflex. Interestingly, metabolism, inflammation and circadian rhythms have all been linked to the development and progression of OA. This article reviews current knowledge of the direct and indirect roles of the nervous system and circadian system in the initiation and/or progression of OA, and highlights the directions for future research in this emerging field.

摘要

骨关节炎(OA)是一种普遍且使人虚弱的关节疾病,已知的风险因素包括衰老、肥胖和慢性炎症。中枢、外周和自主神经系统对于所有代谢系统都是必不可少的,并且有新的证据表明这些系统在 OA 中起作用。在过去的几年中,代谢疾病(如肥胖或糖尿病)与由神经系统严密调节的昼夜节律紊乱有关,而炎症和自身免疫性疾病与胆碱能迷走神经反射的紊乱有关。有趣的是,代谢、炎症和昼夜节律都与 OA 的发生和发展有关。本文综述了神经系统和昼夜节律系统在 OA 发生和/或进展中的直接和间接作用的现有知识,并强调了这一新兴领域未来研究的方向。

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
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Bone. 2016-3

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Nat Rev Rheumatol. 2016-2

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Acta Orthop. 2015

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J Cell Physiol. 2015-9

[10]
Activation of α7 nicotinic acetylcholine receptors prevents monosodium iodoacetate-induced osteoarthritis in rats.

Cell Physiol Biochem. 2015

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