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Effects of Curcumin on High Glucose-Induced Epithelial-to-Mesenchymal Transition in Renal Tubular Epithelial Cells Through the TLR4-NF-κB Signaling Pathway.

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机构: [1]Traditional Chinese Medicine, LiaoningUniversity of Traditional ChineseMedicine, Shenyang, Liaoning Province,110847, People’s Republic of China [2]Department of Nephrology, SecondPeople’s Hospital, The First AffiliatedHospital of Shenzhen University,Shenzhen, Guangdong Province, 518000,People’s Republic of China [3]Departmentof Pathophysiology, China MedicalUniversity, Shenyang, Liaoning Province,110001, People’s Republic of China [4]Department of Physiology, ChinaMedical University, Shenyang, LiaoningProvince, 110001, People’s Republic ofChina [5]Center for Pathophysiology,School of Basic Medicine and ClinicalPharmacy, China PharmaceuticalUniversity, Nanjing, Jiangsu Province,210009, People’s Republic of China
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Diabetic kidney disease (DKD) is a microvascular complication in diabetes mellitus, while tubuloepithelial to mesenchymal transition (EMT) of mature tubular epithelial cells is a key point in the early development and progression of renal interstitial fibrosis. The present study aimed to investigate the protective effects of Curcumin on EMT and fibrosis in cultured normal rat kidney tubular epithelial cell line (NRK-52E). By using immunofluorescence staining and Western blot protocols, in vitro experiments were designed to analyze EMT markers, including collagen I and E-cadherin in high glucose (HG) exposed NRK-52E cells and to detect the expression levels of phosphorylated-NF-κB, TLR4 and reactive oxygen species (ROS) after Curcumin pre-treatment. With co-treatment with TAK242, these molecules in the TLR4-NF-κB signaling pathway were further evaluated. Curcumin decreased the HG-induced EMT levels and ROS production in NRK-52E cells. Furthermore, Curcumin was found to inhibit the TLR4-NF-κB signaling activation in HG-induced EMT of NRK-52E cells. The present study provides evidence suggesting a novel mechanism that Curcumin exerts the anti-fibrosis effects via inhibiting activation of the TLR4-NF-κB signal pathway and consequently protecting the HG-induced EMT in renal tubular epithelial cells. Thereby, TLR4-NF-κB may be a useful target for therapeutic intervention in DKD. © 2021 Liu et al.

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出版当年[2020]版:
大类 | 3 区 医学
小类 | 4 区 内分泌学与代谢
最新[2025]版:
大类 | 3 区 医学
小类 | 4 区 内分泌学与代谢
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出版当年[2019]版:
Q3 ENDOCRINOLOGY & METABOLISM
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Q3 ENDOCRINOLOGY & METABOLISM

影响因子: 最新[2023版] 最新五年平均 出版当年[2019版] 出版当年五年平均 出版前一年[2018版] 出版后一年[2020版]

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第一作者机构: [1]Traditional Chinese Medicine, LiaoningUniversity of Traditional ChineseMedicine, Shenyang, Liaoning Province,110847, People’s Republic of China
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通讯机构: [2]Department of Nephrology, SecondPeople’s Hospital, The First AffiliatedHospital of Shenzhen University,Shenzhen, Guangdong Province, 518000,People’s Republic of China [3]Departmentof Pathophysiology, China MedicalUniversity, Shenyang, Liaoning Province,110001, People’s Republic of China [5]Center for Pathophysiology,School of Basic Medicine and ClinicalPharmacy, China PharmaceuticalUniversity, Nanjing, Jiangsu Province,210009, People’s Republic of China [*1]Department of Nephrology, Second People’s Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, 518000, People’s Republic of China [*2]Center for Pathophysiology, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu Province, 210009, People’s Republic of China
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