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锌缺乏通过Nrf2/HO-1途径调节氧化应激和炎症,加重高脂饮食诱导的肾损伤。

Zinc Deficiency Aggravates High-Fat Diet-Induced Renal Injury by Regulating Oxidative Stress and Inflammation via the Nrf2/HO-1 Pathway.

作者信息

Guan Yucan, Wu Linlin, Wu Man, Zhu Yuexin, Luo Ping, Luo Manyu

机构信息

Department of Nephropathy, The Second Hospital of Jilin University, Changchun, Jilin Province, China.

Pharmacy Intravenous Admixture Service, The Second Hospital of Jilin University, Changchun, Jilin Province, China.

出版信息

Biol Trace Elem Res. 2025 Jun 5. doi: 10.1007/s12011-025-04663-5.

Abstract

Obesity-related kidney disease (ORG) is associated with oxidative stress and inflammation. Zinc plays a crucial role in antioxidative defense, but its deficiency may exacerbate renal injury. The role of Zn deficiency in obesity-induced oxidative stress remains unclear. Male C57BL/6J mice were divided into four groups: ND/NZ (normal diet, normal Zn), ND/LZ (normal diet, low Zn), HFD/NZ (high-fat diet, normal Zn), and HFD/LZ (high-fat diet, low Zn) groups. After 24 weeks, renal function, histopathology, oxidative stress, and inflammatory markers were analyzed. The levels of ROS and key proteins in the Nrf2/HO-1 and PI3K/Akt pathways were assessed via Western blotting and immunofluorescence. An in vitro MPC5 podocyte model was used to examine the effects of Zn under palmitic acid stimulation, with siRNA-mediated Nrf2 knockdown. Zn deficiency exacerbated renal dysfunction, fibrosis, and inflammation in obese mice; increased ROS levels; suppressed Nrf2 signaling; and activated PI3K/Akt. In vitro, Zn supplementation reduced ROS levels and restored Nrf2 nuclear translocation, whereas Nrf2 knockdown aggravated oxidative stress. Zn deficiency promotes obesity-induced renal injury by increasing oxidative stress and inflammation through Nrf2 inhibition and PI3K/Akt activation.

摘要

肥胖相关肾病(ORG)与氧化应激和炎症相关。锌在抗氧化防御中起关键作用,但其缺乏可能会加重肾损伤。锌缺乏在肥胖诱导的氧化应激中的作用仍不清楚。将雄性C57BL/6J小鼠分为四组:正常饮食/正常锌(ND/NZ)组、正常饮食/低锌(ND/LZ)组、高脂饮食/正常锌(HFD/NZ)组和高脂饮食/低锌(HFD/LZ)组。24周后,分析肾功能、组织病理学、氧化应激和炎症标志物。通过蛋白质免疫印迹法和免疫荧光法评估活性氧(ROS)水平以及Nrf2/HO-1和PI3K/Akt信号通路中的关键蛋白。利用体外MPC5足细胞模型,在棕榈酸刺激下,采用小干扰RNA(siRNA)介导的Nrf2基因敲低技术,研究锌的作用。锌缺乏加剧了肥胖小鼠的肾功能障碍、纤维化和炎症;增加了ROS水平;抑制了Nrf2信号传导;并激活了PI3K/Akt。在体外,补充锌可降低ROS水平并恢复Nrf2核转位,而Nrf2基因敲低则加重氧化应激。锌缺乏通过抑制Nrf2和激活PI3K/Akt增加氧化应激和炎症,从而促进肥胖诱导的肾损伤。

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