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Basic Study
Copyright: ©Author(s) 2026.
World J Gastroenterol. Apr 28, 2026; 32(16): 116187
Published online Apr 28, 2026. doi: 10.3748/wjg.v32.i16.116187
Figure 6
Figure 6 Oxymatrine reverses hepatic metabolite changes in metabolic dysfunction-associated steatotic liver disease rats. A: Principal component analysis scores (positive/negative modes); B: Orthogonal partial least squares discriminant analysis score plots (positive and negative ion modes); C: Orthogonal partial least squares discriminant analysis permutation tests: Both ion modes; D: Top 150 hepatic metabolites: Heatmap visualization; E: The levels of adrenic acid, luteolin, oleoylethanolamide and pomiferin in the hepatic metabolites among the three groups, n = 6; F: Enrichment analysis of differential hepatic metabolites in Kyoto Encyclopedia of Genes and Genomes pathways (control, model, oxymatrine). aP < 0.05, bP < 0.01 and cP < 0.001. Statistical analysis was conducted using one-way analysis of variance with Tukey’s post hoc test, and results are presented as mean ± SD. Group A: Control; Group B: Model; Group C: Oxymatrine; NS: Not significant.


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