← Back to research
Our interpretation / GoldJan 2027
Not yet verified
This paper was discovered by the mouse-research search pipeline, but mouse involvement has not been confirmed.Water extract of Persicaria capitata lowers serum ALT in mice
In a whole‑organism mouse model of alcoholic liver injury, daily oral WP significantly reduced serum ALT and AST and lowered hepatic lipid levels.
Editorial projection
gold-editorial-llm-v3
Source
PubMed / NCBI
Mouse involvement
Not yet verified
This paper was discovered by the mouse-research search pipeline, but mouse involvement has not been confirmed.
Our semantic representation
What happened
- ↓serum ALTWP significantly reduced serum ALT.
- ↓serum ASTWP significantly reduced serum AST.
- ↓hepatic lipid levelsWP significantly reduced hepatic lipid levels.
- ↓oxidative stressWP alleviated oxidative stress.
- ↑ZO-1 expressionWP increased ZO-1 expression.
The experiment
What they did
whole-organism studyWP treatment in alcoholic liver injury mouse model
- Water extract of Persicaria capitata (WP)oral · daily
- Water extract of Persicaria capitata (WP)oral · daily
- Water extract of Persicaria capitata (WP)oral · daily
The subjects
Who / what was studied
whole-organism study
- mice
The researchers' voice
Original research
Hepatoprotective effects of Persicaria capitata against alcoholic liver injury by regulating the gut-liver axis via PI3K-Akt and TLR4/NF-κB signaling pathways.
Original abstract
Persicaria capitata, a vital Miao medicine, is traditionally employed to "clear heat and promote diuresis" and "detoxify". In traditional theory, alcoholic liver injury (ALI) is categorized as a "Damp-Heat accumulation" syndrome, often manifesting as damp-heat jaundice. The traditional application of P. capitata in treating jaundice and inflammatory conditions provides a rationale for its hepatoprotective use.
To provide a scientific basis for the traditional use of P. capitata by systematically investigating the protective effects of its water extract (WP) on ALI and exploring the associated molecular mechanisms.
An ALI mouse model was established by alcohol feeding for 28 days. Mice were orally administered with WP (175, 350, 700 mg/kg/day). Liver and intestinal functions were assessed by biochemical assays, histology, transcriptomics, 16S rRNA sequencing, and Western blotting.
WP significantly reduced serum ALT, AST, and hepatic lipid levels while alleviating oxidative stress. Mechanistically, WP regulated the gut-liver axis by maintaining intestinal barrier integrity (increased ZO-1 and Occludin expression) and enriching beneficial Akkermansia bacteria. This restoration of the intestinal barrier subsequently suppressed hepatic inflammatory responses and hepatocyte apoptosis by blocking the LPS-TLR4/NF-κB signaling cascade while simultaneously promoting the PI3K-Akt survival pathway.
By modulating the gut-liver axis-specifically through the restoration of intestinal barrier integrity and the regulation of TLR4/NF-κB and PI3K-Akt signaling-P. capitata effectively mitigates ALI. This study provides a mechanistic rationale for its traditional use and supports its development as a promising intervention for alcoholic liver-related pathologies.