Background: Hepatic ischemia reperfusion injury (HIRI) is considered
one of the most common causes of liver damage and dysfunction.
Oxytocin (OT), besides its classical functions, exhibits a potent antistress,
anti-inflammatory, and antioxidant effects. Aim: This study was
designed to evaluate the effect of pretreatment with OT on HIRI and to
determine its possible protective mechanisms, focusing on the potential
role of NADPH oxidase 2 (NOX2). Methods: 28 adult Wister albino
male rats were divided into 4 groups: group I (control group): received
saline and subjected to surgery without ischemic procedure, group II (OT
group): received OT and subjected to surgery without ischemic
procedure, group III (HIR group): underwent hepatic ischemia
reperfusion (HIR) procedure & group IV (HIR+ OT group): received OT
and underwent HIR procedure. We assessed the effect of OT on serum
liver enzymes, hepatic malondialdehyde (MDA), glutathione (GSH), tumor necrosis factor alfa
(TNFα), and NOX2. Results: HIR caused significant increase in serum liver enzymes, hepatic
MDA, TNFα and NOX2 levels with a significant decrease in GSH level. Administration of OT
caused a significant improvement in all previous parameters, these results were supported by
histopathological examination. Conclusion: OT exerts hepatoprotective effect in HIR-induced
liver injury even in part through NOX2.
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