Proteome profiling, biochemical and histological analysis of diclofenac-induced liver toxicity in Yersinia enterocolitica and Lactobacillus fermentum fed rat model: a comparative analysis.

Diclofenac is a hepatotoxic non-steroidal anti-inflammatory drug (NSAID) that affects liver histology and its protein expression levels. Here, we studied the effect of diclofenac on rat liver when co-administrated with either Yersinia enterocolitica strain 8081 serotype O:8 biovar 1B (DY) or Lactobacillus fermentum strain 9338 (DL). Spectroscopic analysis of stool samples showed biotransformation of diclofenac. When compared with each other, DY rats lack peaks at 1709 and 1198 cm, while DL rats lack peaks at 1411 cm. However, when compared to control, both groups lack peaks at 1379 and 1170 cm. Assessment of serum biomarkers of hepatotoxicity indicated significantly altered activities of AST (DY: 185.65 ± 8.575 vs Control: 61.9 ± 2.607, DL: 247.5 ± 5.717 vs Control: 61.9 ± 2.607), ALT (DY: 229.8 ± 6.920 vs Control: 70.7 ± 3.109, DL: 123.75 ± 6.068 vs Control: 70.7 ± 3.109), and ALP (DY: 276.4 ± 18.154 vs Control: 320.6 ± 9.829, DL: 298.5 ± 12.336 vs Control: 320.6 ± 9.829) in IU/L. The analysis of histological alterations showed hepatic sinusoidal dilation with vein congestion and cell infiltration exclusively in DY rats along with other histological changes that are common to both test groups, thereby suggesting more pronounced alterations in DY rats. Further, LC-MS/MS based label-free quantitation of proteins from liver tissues revealed 74.75% up-regulated, 25.25% down-regulated in DY rats and 51.16% up-regulated, 48.84% down-regulated in DL experiments. The proteomics-identified proteins majorly belonged to metabolism, apoptosis, stress response and redox homeostasis, and detoxification and antioxidant defence that demonstrated the potential damage of rat liver, more pronounced in D*Y rats. Altogether the results are in favor that the administration of lactobacilli somewhat protected the rat hepatic cells against the diclofenac-induced toxicity.