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DW14006 作为一种直接 AMPKα 激活剂可改善小鼠糖尿病周围神经病变。

DW14006 as a Direct AMPKα Activator Ameliorates Diabetic Peripheral Neuropathy in Mice.

机构信息

Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.

Department of Medicinal Chemistry, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.

出版信息

Diabetes. 2020 Sep;69(9):1974-1988. doi: 10.2337/db19-1084. Epub 2020 Jul 9.

Abstract

Diabetic peripheral neuropathy (DPN) is a long-term complication of diabetes with a complicated pathogenesis. AMP-activated protein kinase (AMPK) senses oxidative stress, and mitochondrial function plays a central role in the regulation of DPN. Here, we reported that DW14006 (2-[3-(7-chloro-6-[2'-hydroxy-(1,1'-biphenyl)-4-yl]-2-oxo-1,2-dihydroquinolin-3-yl)phenyl]acetic acid) as a direct AMPKα activator efficiently ameliorated DPN in both streptozotocin (STZ)-induced type 1 and BKS type 2 diabetic mice. DW14006 administration highly enhanced neurite outgrowth of dorsal root ganglion neurons and improved neurological function in diabetic mice. The underlying mechanisms have been intensively investigated. DW14006 treatment improved mitochondrial bioenergetics profiles and restrained oxidative stress and inflammation in diabetic mice by targeting AMPKα, which has been verified by assay against the STZ-induced diabetic mice injected with adeno-associated virus 8-AMPKα-RNAi. To our knowledge, our work might be the first report on the amelioration of the direct AMPKα activator on DPN by counteracting multiple risk factors including mitochondrial dysfunction, oxidative stress, and inflammation, and DW14006 has been highlighted as a potential leading compound in the treatment of DPN.

摘要

糖尿病周围神经病变(DPN)是糖尿病的一种长期并发症,其发病机制复杂。AMP 激活的蛋白激酶(AMPK)可感知氧化应激,而线粒体功能在调节 DPN 中起着核心作用。在这里,我们报告了作为一种直接的 AMPKα 激活剂的 DW14006(2-[3-(7-氯-6-[2'-羟基-(1,1'-联苯)-4-基]-2-氧代-1,2-二氢喹啉-3-基)苯基]乙酸)可有效改善链脲佐菌素(STZ)诱导的 1 型和 BKS 2 型糖尿病小鼠的 DPN。DW14006 给药可显著促进背根神经节神经元的轴突生长,并改善糖尿病小鼠的神经功能。我们已经深入研究了其潜在机制。DW14006 通过靶向 AMPKα 改善了糖尿病小鼠的线粒体生物能谱,并抑制了氧化应激和炎症,这已通过用 STZ 诱导的注射腺相关病毒 8-AMPKα-RNAi 的糖尿病小鼠的检测得到证实。据我们所知,我们的工作可能是首次报道直接的 AMPKα 激活剂通过对抗包括线粒体功能障碍、氧化应激和炎症在内的多种风险因素改善 DPN,DW14006 已被突出为治疗 DPN 的潜在先导化合物。

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