Abstract: Objective To investigate the effects of Qingre Jiedu Huazhuo tablets on ADP, TNF-α and IL-10 in
rat model of fatty liver disease. Methods The rat liver inflammation model was established by feeding high
sugar, fat and liquor. The rats were randomly divided into normal group, model group, Fenofibrate group and
Qingre Jiedu Huazhuo group, 10 rats in each group. Qingre Jiedu Huazhuo tablets (0.081 g/ml) and Fenofibrate
(0.083 g/ml) were used to treat liver inflammatory model rat for 30 days [1 ml/(100g·d)], respectively. The
content of blood serum alanine transaminase (ALT), aspartate transaminase (AST), triglyceride (TG) and total
cholesterin (TC) were measured by colorimetry; tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10) and
adiponectin (ADP) were measured by enzyme-linked immumsorbent assay (ELISA). Pathologic changes of
liver were measured by a microscope, and the two-step method of immunohistochemistry (IH) was adopted
to test the expression of TNF-α and IL-10 in live tissues. Results Light microscopic inspection: Qingre Jiedu
Huazhuo tablets can suppress liver inflammation and lipid deposition. The expression of serum TG, TCHO,
ALT, AST and TNF-α in model group were significantly higher than those in normal control group (P = 0.000,
0.006, 0.005, 0.005, 0.000, respectively). The expression of ADP in model group was significantly lower
than that in normal group (P = 0.005). Compared with the model group, the expression of TG, TCHO, ALT,
AST and TNF-α were significantly lower in Qingre Jiedu Huazhuo tablets group (P = 0.000). The expression
of ADP and IL-10 were significantly higher in Qingre Jiedu Huazhuo tablets group (P = 0.02, 0.000). Qingre
Jiedu Huazhuo tablets can significantly reduce the level of TNF-α (P = 0.000) and increase the level of IL-10
(P = 0.000). Conclusions Qingre Jiedu Huazhuo tablets can regulate lipid metabolism and resist inflammatory
injury, which may be associated with the reduced release of promoting inflammatory cytokines TNF-α and the
promoting of the expression of anti-inflammatory cytokine IL-10 and adipokine ADP.
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