This study aimed to demonstrate protective activities of the
narirutin fraction from peels of Citrus unshiu against
ethanol-induced hepatic damage through an animal study. Citrus
narirutin fraction (CNF), contained 75% of
narirutin, was obtained by an ultra-sonicated extraction and further purification. ICR mice were divided into four groups; normaldiet control,
ethanol control (6.5g
ethanol/kg), low-CNF (ethanol+150mg CNF/kg) and high-CNF (ethanol+300mg CNF/kg) groups. Consumption of alcohol for 8weeks induced severe liver damage with increases in prognostic indicators such as
aspartate transaminase,
alanine transaminase in serum whereas co-administration of CNF suppressed their increases. Excessive accumulations in liver TG and TC in
ethanol control group were also suppressed by co-administration of CNF. Co-administration of CNF maintained SOD activity, GSH and
malondialdehyde levels close to those of the normal diet group. Chronic consumption of alcohol also stimulated abrupt increases in pro-inflammatory
cytokines such as nuclear factor (NF)-κB,
tumor necrosis factor (TNF)-α and
interleukin (IL)-1β in liver otherwise co-administration of CNF effectively suppressed production of these
cytokines dose-dependently. These results indicate that co-administration of CNF with alcohol can alleviate alcohol induced liver damage through preventing
lipid formation, protecting
antioxidant system and suppressing productions of pro-inflammatory
cytokines.