Hepatoprotective and anti-inflammatory effects of entecavir or probiotics on Oxaliplatin-Induced Liver Injury in the rats.

Abstract

Oxaliplatin (OXA), a current cancer chemotherapeutic, has low efficacy and is linked to
serious adverse effects, including liver damage. We anticipated that probiotics and
entecavir would help reduce OXA-induced liver damage because the pathophysiology of
drug-induced liver damage is thought to be related to the disordered gut microbiota.
Twenty-four rats were used in this study and divided into 4 groups: control group (n=6),
OXA group (n=6), entecavir (ENT) group (n=6), and probiotics (PRO) group (n=6). After
3 weeks, all rats were sacrificed, and blood samples were analyzed for alkaline
phosphatase (ALP), alanine aminotransferase (ALT) and aspartate aminotransferase (AST),
interleukin 6 (IL-6), and IL-1. Serum measurement of biochemical parameters showed a
significant increase in ALP in the OXA group compared to the control group (p<0.0001).
The treatment with ENT or PRO along with OXA alleviated these changes. Significant
elevation of serum ALT (p=0.041) and non-significant (p=0.210) increase of AST was
observed in OXA-treated rats as compared with control rats. The administration of ENT or
PRO along OXA restored these changes, but they did not reach the levels of control rats.
Significant elevations of serum IL-1 (p=0.024) and a non-significant (p=0.114) increase of
IL-6 were observed in OXA-treated rats compared to control rats. The administration
of ENT or PRO along OXA reduced inflammatory cytokines' levels but they did not return to
the baseline. The treatment with ENT or PRO was beneficial in reducing the severity of
OXA-induced liver injury, likely by reducing inflammatory responses and liver function
tests.