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AMPK 通过控制氧化应激负调控 RANKL 诱导的破骨细胞分化。

AMPK negatively regulates RANKL-induced osteoclast differentiation by controlling oxidative stress.

机构信息

Department of Nutritional Science and Food Safety, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502, Japan; The Nippon Foundation Human Milk Bank, 17-10 Nihonbashi-koamicho, Chuo-ku, Tokyo, 103-0016, Japan.

Department of Nutritional Science and Food Safety, Faculty of Applied Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502, Japan.

出版信息

Free Radic Biol Med. 2023 Aug 20;205:107-115. doi: 10.1016/j.freeradbiomed.2023.05.033. Epub 2023 Jun 1.

Abstract

AMP-activated protein kinase (AMPK) is a crucial energy sensor of cellular metabolism under various metabolic stresses, such as oxidative stress and inflammation. AMPK deficiency increases osteoclast numbers and reduces bone mass; however, the precise mechanisms remain unclear. This study aimed to clarify the mechanistic connection between AMPK and osteoclast differentiation, and the potential role of AMPK in the anti-resorptive effects of several phytochemicals. We found that receptor activator of nuclear factor-kappa B (NF-κB) ligand (RANKL)-induced osteoclast differentiation, osteoclastic gene expression, and activation of mitogen-activated protein kinase (MAPK) and NF-κB were promoted in cells transfected with AMPK siRNA. AMPK knockdown led to defective synthesis of heme oxygenase-1, an antioxidant enzyme, and the upstream mediator, nuclear factor erythroid-2-related factor 2. Furthermore, treatment with N-acetyl-l-cysteine, an antioxidant, abolished osteoclast differentiation and MAPK/NF-κB activation induced by AMPK knockdown. AMPK activators, hesperetin, gallic acid, resveratrol, and curcumin, suppressed osteoclast differentiation via the activation of AMPK. These results suggest that AMPK inhibits RANKL-induced osteoclast differentiation by enhancing antioxidant defense system and regulating oxidative stress. AMPK activation by dietary-derived phytochemicals may be effective for the treatment of bone diseases.

摘要

腺苷酸活化蛋白激酶 (AMPK) 是细胞代谢在各种代谢应激下的重要能量传感器,如氧化应激和炎症。AMPK 缺乏会增加破骨细胞数量并减少骨量;然而,确切的机制仍不清楚。本研究旨在阐明 AMPK 与破骨细胞分化之间的机制联系,以及 AMPK 在几种植物化学物质的抗吸收作用中的潜在作用。我们发现,转染 AMPK siRNA 的细胞中,核因子-κB 受体激活剂(RANKL)诱导的破骨细胞分化、破骨细胞基因表达以及丝裂原活化蛋白激酶(MAPK)和 NF-κB 的激活均得到促进。AMPK 敲低导致抗氧化酶血红素加氧酶-1和上游介质核因子红系 2 相关因子 2 的合成缺陷。此外,抗氧化剂 N-乙酰-L-半胱氨酸的处理消除了 AMPK 敲低诱导的破骨细胞分化和 MAPK/NF-κB 激活。AMPK 激活剂橙皮苷、没食子酸、白藜芦醇和姜黄素通过激活 AMPK 抑制破骨细胞分化。这些结果表明,AMPK 通过增强抗氧化防御系统和调节氧化应激来抑制 RANKL 诱导的破骨细胞分化。膳食衍生的植物化学物质激活 AMPK 可能是治疗骨病的有效方法。

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