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营养保健品在骨关节炎生物学中的作用:关注营养基因组学的作用。

Nutraceutical Activity in Osteoarthritis Biology: A Focus on the Nutrigenomic Role.

机构信息

Department of Medical and Surgical Sciences, Alma Mater Studiorum - University of Bologna, 40126 Bologna, Italy.

Laboratory of Immunorheumatology and Tissue Regeneration, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.

出版信息

Cells. 2020 May 16;9(5):1232. doi: 10.3390/cells9051232.

Abstract

Osteoarthritis (OA) is a disease associated to age or conditions that precipitate aging of articular cartilage, a post-mitotic tissue that remains functional until the failure of major homeostatic mechanisms. OA severely impacts the national health system costs and patients' quality of life because of pain and disability. It is a whole-joint disease sustained by inflammatory and oxidative signaling pathways and marked epigenetic changes responsible for catabolism of the cartilage extracellular matrix. OA usually progresses until its severity requires joint arthroplasty. To delay this progression and to improve symptoms, a wide range of naturally derived compounds have been proposed and are summarized in this review. Preclinical in vitro and in vivo studies have provided proof of principle that many of these nutraceuticals are able to exert pleiotropic and synergistic effects and effectively counteract OA pathogenesis by exerting both anti-inflammatory and antioxidant activities and by tuning major OA-related signaling pathways. The latter are the basis for the nutrigenomic role played by some of these compounds, given the marked changes in the transcriptome, miRNome, and methylome. Ongoing and future clinical trials will hopefully confirm the disease-modifying ability of these bioactive molecules in OA patients.

摘要

骨关节炎(OA)是一种与年龄相关的疾病,或是能引发关节软骨老化的疾病,关节软骨是一种有丝分裂后组织,在主要的体内平衡机制失效之前一直保持功能。OA 会引起疼痛和残疾,严重影响国家卫生系统的成本和患者的生活质量。OA 是一种全关节疾病,由炎症和氧化信号通路以及负责软骨细胞外基质分解代谢的明显表观遗传变化维持。OA 通常会进展,直到其严重程度需要进行关节置换术。为了延缓这种进展并改善症状,已经提出了广泛的天然来源化合物,并在本综述中进行了总结。临床前的体外和体内研究已经提供了原理性证据,证明其中许多营养保健品能够发挥多效性和协同作用,并通过发挥抗炎和抗氧化作用以及调节主要的 OA 相关信号通路,有效地对抗 OA 的发病机制。鉴于转录组、miRNome 和甲基组发生了明显的变化,后者是这些化合物中一些具有营养基因组作用的基础。正在进行和未来的临床试验有望证实这些生物活性分子在 OA 患者中的疾病修饰能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd6e/7291002/258a7e366474/cells-09-01232-g001.jpg

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