AI Article Synopsis

  • Salvianolic acid C (SAC) is a natural compound that may protect against kidney diseases, specifically by targeting tubulointerstitial fibrosis in the kidneys.* -
  • Experiments using mouse models and human kidney cells showed that SAC treatment reduced fibrosis levels and inhibited related protein expressions, suggesting a protective role against kidney damage.* -
  • The study concluded that SAC works by inhibiting epithelial-mesenchymal transition (EMT) and operates through the TGF-β/Smad signaling pathway to alleviate kidney fibrosis.*

Article Abstract

Background: Salvianolic acid C (SAC) is a natural compound derived from that can protect against renal diseases. The aims of this work were to explore the effect of SAC on kidney tubulointerstitial fibrosis and study the associated mechanism.

Methods: Models for unilateral ureteral obstruction (UUO) and aristolochic acid I (AAI) were established in mice to study renal tubulointerstitial fibrosis. Rat kidney fibroblasts (NRK-49F) and human kidney epithelial cells (HK2) were used as cellular models to evaluate the effects of SAC on kidney fibrosis.

Results: Treatment with SAC for two weeks reduced the level of renal tubulointerstitial fibrosis in UUO- and AAI-induced fibrotic kidneys, as demonstrated by Masson's staining and Western blot. SAC inhibited extracellular matrix protein expression in NRK-49F cells and TGF-β-stimulated HK2 cells in dose-dependent fashion. Moreover, SAC inhibited the expression of epithelial-mesenchymal transition (EMT) factors in animal and cellular models of kidney fibrosis, as well as the EMT-related transcription factor snail. Furthermore, SAC inhibited the fibrosis-related signaling pathway Smad3 in the fibrotic kidneys of two mouse models and in renal cells.

Conclusions: We conclude that SAC inhibits EMT and ameliorates tubulointerstitial fibrosis through involvement of the signaling pathway for transforming growth factor-β (TGF-β)/Smad.

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Source
http://dx.doi.org/10.31083/j.fbl2806121DOI Listing

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