Journal of Ethnopharmacology, Journal Year: 2024, Volume and Issue: 334, P. 118572 - 118572
Published: July 16, 2024
Language: Английский
Journal of Ethnopharmacology, Journal Year: 2024, Volume and Issue: 334, P. 118572 - 118572
Published: July 16, 2024
Language: Английский
Phytomedicine, Journal Year: 2025, Volume and Issue: unknown, P. 156664 - 156664
Published: March 1, 2025
Language: Английский
Citations
0Journal of Ethnopharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 119398 - 119398
Published: Jan. 1, 2025
Language: Английский
Citations
0Naunyn-Schmiedeberg s Archives of Pharmacology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 13, 2025
Language: Английский
Citations
0Scientific Reports, Journal Year: 2025, Volume and Issue: 15(1)
Published: March 28, 2025
This study investigates the role of miR-203 in regulating renal cell injury diabetic nephropathy by targeting suppressor cytokine signaling (SOCS) proteins SOCS6 and SOCS7. Using NRK cells, we assessed apoptosis through flow cytometry TUNEL assays, while real-time quantitative PCR (RT-PCR) quantified miRNA mRNA expressions. Cell viability was measured using CCK-8 assay, levels were determined ELISA. We also evaluated reactive oxygen species (ROS) malondialdehyde (MDA) with specific assay kits. The dual luciferase confirmed interaction Western blotting analyzed protein key molecules including JAK1, p-JAK1, JAK2, p-JAK2, STAT3, p-STAT3.Our findings revealed that high glucose (HG) treatment reduced levels, leading to decreased proliferation, increased concentrations (TNF-α, IL-1β, IL-4, IL-6), heightened ROS MDA apoptosis. Notably, mimics counteracted HG's detrimental effects, inhibitors exacerbated them. Mechanistically, directly SOCS7 expression, thereby inhibiting JAK/STAT3 signaling. Thus, provides protective effects against modulating SOCS their associated pathways.
Language: Английский
Citations
0Open Medicine, Journal Year: 2025, Volume and Issue: 20(1)
Published: Jan. 1, 2025
Abstract Introduction Diabetic kidney disease (DKD) represents serious diabetes-associated complications, and podocyte loss is an important histologic sign of DKD. The cellular molecular profiles podocytes in DKD have yet to be fully elucidated. Methods This study analyzed kidney-related single-nucleus RNA-seq datasets (GSE131882, GSE121862, GSE141115) human diabetic glomeruli transcriptome profiling (GSE30122). ARHGAP28 expression was validated by western blot immunohistochemistry. Results In tissues, 154 differentially expressed genes (DEGs) were identified podocytes, which enriched biological processes related nephron development extracellular matrix–receptor interactions. Similarly, the mouse kidney, 344 DEGs found, clustering pathways associated with renal signaling mechanisms like PI3K/Akt (phosphatidylinositol-3 kinase/protein kinase B) PPAR (peroxisome proliferator-activated receptor). glomeruli, 438 identified, showing significant enrichment nephropathy. Venn analysis revealed 22 common across being notably overexpressed podocytes. nephropathy model using db/db mice showed that significantly upregulated cortex glomeruli. vitro studies a high-glucose corroborated these findings. Conclusions Collectively, this provides insight into function diagnosis indicates potential biomarker
Language: Английский
Citations
0Journal of Ethnopharmacology, Journal Year: 2024, Volume and Issue: 334, P. 118572 - 118572
Published: July 16, 2024
Language: Английский
Citations
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