ArticleAdvanced biomedical research2025
Investigating the Effect of Secretome Secreted from Adult Rat Kidney-Derived Stem Cells on the Expression of miR375, miR494 and Tissue Changes in Glycerol-Induced Acute Kidney Injury.
Article in Advanced biomedical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Renoprotection by 5-Methoxytryptophan in Kidney Disease.Biomolecules · 2026Review
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Acute kidney injury (AKI) causes high mortality. Cell therapy has provided acceptable results, but factors such as immune rejection and teratoma formation have limited their use. The purpose of this research is to study the reparative effects of secretome secreted from kidney-derived stem cells on glycerol-induced kidney damage in rats. Materials and Methods: Secretomes were isolated from conditioned media of kidney mesenchymal stem cells. The animals were separated into 4 groups: Control, Secretome (received 30 μg/kg secretome, for 3 days), Glycerol (10 ml/kg of glycerol, intramuscularly) and Glycerol + Secretome (received glycerol and secretome). Blood urea (BUN), Creatinine (Cr) and Albumin (alb) levels were measured with detection kits. The histopathological results of the secretomes on kidney were checked with PAS staining and the amount of expression of miR-375 and miR-494 was assessed by quantitative real-time polymerase chain reaction (qRT-PCR). Results: The results of this research showed that intravenous of secretomes significantly decreased the levels of BUN ( Conclusion: The results of this research showed that secretomes extracted from kidney stem cells can play a role in reducing kidney damage by regulating miRNAs related to AKI.
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