Objective: This study evaluated the protective effect of D-limonene against ethanol-induced hepatic injury in
rats and analyzed the associated mechanisms. Methods: The alcoholic liver disease (ALD) model of rats was established
by administration of 50% alcohol. Seven groups of mice were created, namely blank control (A), alcoholic damage model
(B), low-dose D-limonene (C), middle-dose D-limonene (D), high-dose D-limonene (E), high-dose D-limonene blank
(F), and diammonium glycyrrhizinate (DG) control (G) groups. Group A was daily administered by gavage with distilled
water at a volume of 8 mL/(kg·d) first for two weeks followed by 8 mL/(kg·d) for another four weeks, Group B was
administered with 50% aqueous by the same schedule as for group A, Groups C, D and E were respectively given 100, 200
and 400 mL/(kg·d) D-limonene in 50% aqueous ethanol at the same volume as that used for groups A and B, Group F was
daily administered with 400 mL/(kg·d) D-limonene without alcohol-induced liver injury, and Group G was treated with
200 mL/(kg·d) of DG. HE staining and electronic microscopic evaluation were conducted for examining the morphology
and ultrastructure of liver tissues. The levels of alanine transaminase (ALT), aspartate transaminase (AST), phosoporic acid
(ALP), cholinesterase (CHE), triglyceride (TG), cholesterol (CHO), and low-density lipoprotein-cholesterol (LDL-C) were
detected. Results: Normal liver tissue structure was observed in Group A. Many secondary lysosomes were observed in
Group B. A small amount of lipid droplets was observed in Group C while Golgi was normal and mitochondria was clear.
Normal mitochondria were observed in Group D. Normal mitochondria and Golgi were observed in Group E. The organelles
without abnormalities were observed in Group F. Normal mitochondria were observed in Group G. Serum ALT, AST, ALP,
CHE, TG, CHO and LDL-C were higher in group B than in other groups (P < 0.05); serum levels of the indicators measured
were reduced in different D-limonene groups at various doses than those in alcohol model group (P < 0.05). Conclusion:
D-limonene can ameliorate the damage of ultrastructure in liver tissues, reduce serum indexes caused by alcohol exposure
and the body’s lipids. Moreover, it has a regulatory role in lipid metabolism disorders caused by alcohol.