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脂联素受体激动剂 AdipoRon 对椎间盘退变的抗炎作用。

Anti-Inflammatory Effects of Adiponectin Receptor Agonist AdipoRon against Intervertebral Disc Degeneration.

机构信息

Department of Orthopaedic Surgery, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.

出版信息

Int J Mol Sci. 2023 May 10;24(10):8566. doi: 10.3390/ijms24108566.

Abstract

Adiponectin, a hormone secreted by adipocytes, has anti-inflammatory effects and is involved in various physiological and pathological processes such as obesity, inflammatory diseases, and cartilage diseases. However, the function of adiponectin in intervertebral disc (IVD) degeneration is not well understood. This study aimed to elucidate the effects of AdipoRon, an agonist of adiponectin receptor, on human IVD nucleus pulposus (NP) cells, using a three-dimensional in vitro culturing system. This study also aimed to elucidate the effects of AdipoRon on rat tail IVD tissues using an in vivo puncture-induced IVD degeneration model. Analysis using quantitative polymerase chain reaction demonstrated the downregulation of gene expression of proinflammatory and catabolic factors by interleukin (IL)-1β (10 ng/mL) in human IVD NP cells treated with AdipoRon (2 μM). Furthermore, western blotting showed AdipoRon-induced suppression of p65 phosphorylation ( < 0.01) under IL-1β stimulation in the adenosine monophosphate-activated protein kinase (AMPK) pathway. Intradiscal administration of AdipoRon was effective in alleviating the radiologic height loss induced by annular puncture of rat tail IVD, histomorphological degeneration, production of extracellular matrix catabolic factors, and expression of proinflammatory cytokines. Therefore, AdipoRon could be a new therapeutic candidate for alleviating the early stage of IVD degeneration.

摘要

脂联素是一种由脂肪细胞分泌的激素,具有抗炎作用,参与肥胖、炎症性疾病和软骨疾病等多种生理和病理过程。然而,脂联素在椎间盘(IVD)退变中的功能尚不清楚。本研究旨在使用三维体外培养系统阐明脂联素受体激动剂 AdipoRon 对人椎间盘核(NP)细胞的作用。本研究还旨在使用体内穿刺诱导的 IVD 退变模型阐明 AdipoRon 对大鼠尾 IVD 组织的作用。定量聚合酶链反应分析表明,AdipoRon(2 μM)处理的人 IVD NP 细胞中白细胞介素(IL)-1β(10 ng/mL)下调促炎和分解代谢因子的基因表达。此外,Western blot 显示 AdipoRon 诱导 AMPK 通路中 p65 磷酸化(<0.01)抑制。椎间盘内给予 AdipoRon 可有效缓解大鼠尾 IVD 环状穿刺引起的放射学高度损失、组织形态学退变、细胞外基质分解代谢因子的产生和促炎细胞因子的表达。因此,AdipoRon 可能是缓解 IVD 退变早期的一种新的治疗候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8a7/10217873/24488f8a2d02/ijms-24-08566-g001.jpg

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