Heat shock protein 70 (HSP70) reduces hepatic inflammatory and oxidative damage in a rat model of liver ischemia/reperfusion injury with hyperbaric oxygen preconditioning

Abstract

Background: Several clinical conditions can cause hepatic ischemia/reperfusion (I/R) injury. This study aimed to determine the mechanism of the protective effect of hyperbaric oxygen preconditioning (HBO 2 P) on hepatic ischemia/reperfusion (I/R) injury in a rat model, and to investigate the effects on HBO 2 P and I/R injury of blocking HSP70 using antibody (Ab) pretreatment. Material/Methods: Male Sprague-Dawley rats underwent HBO 2 P for 60 min at 2.0 atmosphere absolute (ATA) pressure for five consecutive days before surgical hepatic I/R injury, performed by clamping the portal vein and hepatic lobe. Four groups studied included: the non-HBO 2 P+ non-I/R group, which underwent sham surgery (N=10); the non-HBO 2 P + I/R group (N=10); the HBO 2 P + I/R group (N=10); and the HBO 2 P + HSP70-Ab + I/R group (N=10) received one dose of HSP70 antibody one day before hepatic I/R injury. Serum lactate dehydrogenase (LDH), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and pro-inflammatory cytokines, tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and hepatic malondialdehyde (MDA) and myeloperoxidase (MPO) were measured biochemically. Rat liver tissues were examined histologically. Results: In rats with hepatic I/R injury without HSP70 antibody pre-treatment, HBO 2 P significantly reduced hepatic injury and levels of LDH, AST, ALT, TNF-α, IL-6, MDA, and MPO levels; in comparison, the group pre-treated with an antibody to inhibit HSP70 (the HBO 2 P + HSP70-Ab + I/R group) showed significant reversal of the beneficial effects of HBO 2 P on hepatic I/R injury (p<0.05). Conclusions: In a rat model of hepatic I/R injury with HBO 2 P, HSP70 reduced hepatic inflammatory and oxidative damage.