ArticleApplied biochemistry and biotechnology2026
Luling Anshen Granules, a Novel Traditional Chinese Medicine formulation, Mitigates Renal Fibrosis in Mice with Chronic Renal Failure by Suppressing the Wnt/β-catenin Signaling Pathway.
Article in Applied biochemistry and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Chronic renal failure (CRF) is an escalating global health concern, imposing substantial economic and health challenges. Traditional Chinese medicine (TCM) offers potential treatments. Luling Anshen Granules (LLASG), a patented multi-herb formula used clinically for kidney disorders, have shown promise in preclinical studies, though their mechanisms remain unclear. A CRF mouse model was induced with a 2.5% adenine suspension. Mice were allocated into six groups: control, CRF model, Urotoxin Qing Granules (UCG) positive control, and three groups treated with LLASG at doses of 2.5, 5, and 10 g/kg. Renal function was evaluated after 4 weeks using blood urea nitrogen, serum creatinine, and 24-hour urinary protein measurements. Renal tissues underwent examination through hematoxylin and eosin, Masson, and TUNEL staining techniques. Protein and gene expressions were analyzed by Western blot, RT-qPCR, immunohistochemistry, and immunofluorescence. A β-catenin knockdown experiment was conducted, and LLASG’s biocompatibility and safety were evaluated in cardiac and hepatic tissues. LLASG enhanced renal function in a dose-dependent fashion, reducing serum blood urea nitrogen and creatinine levels by approximately 30–40% at the highest dose compared with CRF mice, decreased renal tissue damage and apoptosis, and alleviated renal inflammation through NF-κB pathway inhibition. It mitigated renal fibrosis by suppressing the Wnt/β-catenin pathway. β-catenin knockdown diminished the therapeutic effects of LLASG, confirming its mechanistic role. LLASG produced no observable cardiac or hepatic toxicity under the conditions tested, indicating acceptable short-term biocompatibility. Overall, LLASG ameliorates renal dysfunction, inflammation, and fibrosis in CRF mice by suppressing the Wnt/β-catenin pathway.
Indexed as
Identifiers
41670945What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.