AI Article Synopsis

  • - Fu-Fang-Jin-Qian-Cao is a traditional Chinese herbal remedy aimed at treating urinary stones by protecting kidney cells from damage caused by calcium oxalate and oxidative stress, although its exact mechanisms are still under investigation.
  • - The study utilized comprehensive metabolomics and network pharmacology to analyze how Fu-Fang-Jin-Qian-Cao inhibits autophagy in a mouse model of renal injury induced by calcium oxalate, identifying several key proteins involved in this process.
  • - Results indicated that treatment with Fu-Fang-Jin-Qian-Cao effectively reversed damage related to two major signaling pathways (MAPK and PI3K-Akt) and restored the function of several autophagy-related proteins, suggesting its potential in mitigating kidney

Article Abstract

Introduction: Fu-Fang-Jin-Qian-Cao is a Chinese herbal preparation used to treat urinary calculi. Fu-Fang-Jin-Qian-Cao can protect renal tubular epithelial cells from calcium oxalateinduced renal injury by inhibiting ROS-mediated autopathy. The mechanism still needs further exploration. Metabonomics is a new subject; the combination of metabolomics and network pharmacology can find pathways for drugs to act on targets more efficiently.

Methods: Comprehensive metabolomics and network pharmacology to study the mechanism of Fu-Fang-Jin-Qian-Cao inhibiting autophagy in calcium oxalate-induced renal injury. Based on UHPLC-Q-TOF-MS, combined with biochemical analysis, a mice model of Calcium oxalateinduced renal injury was established to study the therapeutic effect of Fu-Fang-Jin-Qian-Cao. Based on the network pharmacology, the target signaling pathway and the protective effect of Fu- Fang-Jin-Qian-Cao on Calcium oxalate-induced renal injury by inhibiting autophagy were explored. Autophagy-related proteins LC3-II, BECN1, ATG5, and ATG7 were studied by immunohistochemistry.

Results: Combining network pharmacology and metabolomics, 50 differential metabolites and 2482 targets related to these metabolites were found. Subsequently, the targets enriched in PI3KAkt, MAPK and Ras signaling pathways. LC3-II, BECN1, ATG5 and ATG7 were up-regulated in Calcium oxalate-induced renal injury. All of them could be reversed after the Fu-Fang-Jin-Qian- Cao treatment.

Conclusions: Fu-Fang-Jin-Qian-Cao can reverse ROS-induced activation of the MAPK signaling pathway and inhibition of the PI3K-Akt signaling pathway, thereby reducing autophagy damage of renal tubular epithelial cells in Calcium oxalate-induced renal injury.

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Source
http://dx.doi.org/10.2174/1386207326666230515151302DOI Listing

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