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葡萄籽原花青素通过 DPP4-Sirt1 通路抑制软骨细胞凋亡和衰老,改善骨关节炎。

Grape seed procyanidins suppress the apoptosis and senescence of chondrocytes and ameliorates osteoarthritis via the DPP4-Sirt1 pathway.

机构信息

Affiliated Yueqing Hospital of Wenzhou Medical University, Department of Orthopaedics, Wenzhou, Zhejiang, China..

出版信息

Food Funct. 2020 Dec 1;11(12):10493-10505. doi: 10.1039/d0fo01377c. Epub 2020 Nov 11.

Abstract

Osteoarthritis (OA) is a complicated pathological condition affecting thousands of people around world, many with substantial unmet medical care needs and without any effective therapies. Previous study has indicated that glucagon-like peptide-1 (GLP-1) is involved in the pathological progress of osteoarthritis; however, the role of dipeptidase-4 (DPP4), which regulates the degradation of GLP-1, still remains unclear in osteoarthritis. Herein, after comparing normal mouse cartilage tissues with OA mouse cartilage tissues by histological analysis, we found out that DPP4 was highly expressed in OA cartilage tissues. To investigate the role of DPP4 in osteoarthritis, the apoptosis and senescence of chondrocytes were found to be decreased in vitro when DPP4 was downregulated by siRNA in chondrocytes. Further study showed that the inhibition of DPP4 by procyanidins, a grape seed extract, attenuated apoptosis and senescence of chondrocytes in vitro. Furthermore, the results showed that DPP4 inhibition protects cartilage by activating Sirt1, which has been reported to be associated with many pathophysiological processes, particularly in age-related diseases, such as neurodegenerative disorders and osteoarthritis. In addition, animal experiment results demonstrated that procyanidins were capable of ameliorating the progression of osteoarthritis through the inhibition of DPP4. This study provides a competitive target for the therapeutic treatment of osteoarthritis, and procyanidins were shown to be a potential medicine for the restoration of the effects of osteoarthritis.

摘要

骨关节炎(OA)是一种复杂的病理状况,影响着全球成千上万的人,其中许多人有大量未满足的医疗需求,且没有任何有效的治疗方法。先前的研究表明,胰高血糖素样肽-1(GLP-1)参与骨关节炎的病理进展;然而,调节 GLP-1 降解的二肽基肽酶-4(DPP4)在骨关节炎中的作用仍不清楚。在此,通过组织学分析比较正常小鼠软骨组织和 OA 小鼠软骨组织后,我们发现 DPP4 在 OA 软骨组织中高度表达。为了研究 DPP4 在骨关节炎中的作用,我们发现当用 siRNA 下调软骨细胞中的 DPP4 时,体外培养的软骨细胞凋亡和衰老减少。进一步的研究表明,葡萄籽提取物原花青素通过抑制 DPP4 减轻了体外软骨细胞的凋亡和衰老。此外,研究结果表明,DPP4 抑制通过激活 Sirt1 来保护软骨,Sirt1 已被报道与许多病理生理过程有关,特别是在与年龄相关的疾病中,如神经退行性疾病和骨关节炎。此外,动物实验结果表明,原花青素通过抑制 DPP4 能够改善骨关节炎的进展。本研究为骨关节炎的治疗提供了一个有竞争力的靶点,原花青素被证明是一种恢复骨关节炎效应的潜在药物。

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