Journal of Practical Hepatology ›› 2023, Vol. 26 ›› Issue (3): 324-327.doi: 10.3969/j.issn.1672-5069.2023.03.006

• Hepatitis in mice • Previous Articles     Next Articles

Protective effect of glycogen synthase kinase 3β inhibitor TDZD-8 on liver injuries in mice with D-Gal/LPS-induced acute liver failure

Zhang Danmei , Shi Chunxia , Chen Qian, et al.   

  1. Department of Infectious Diseases, People’s Hospital, Wuhan University , Wuhan 430060 , Hubei Province, China
  • Received:2022-06-07 Online:2023-05-10 Published:2023-05-08

Abstract: Objective The aim of this study was to investigate the protective effect of glycogen synthase kinase 3β (GSK3β) inhibitor TDZD-8 on liver injuries in mice with D-Gal/LPS-induced acute liver failure(ALF). Methods Twenty-four male mice were randomly divided into control, model and TDZD-8-intervened group, with eight in each. The model of ALF was established by intraperitoneal injection of D-Gal/LPS. Serum free DNA (cf-DNA) was detected by fluorescent dye, and liver homogenate tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were assayed by ELISA. The hepatic expression of L-18, IL-1β, UNC-51-like kinase 1 (ULK1), Beclin 1 and P62 were detected by Western blotting. Results Serum ALT, AST and total bilirubin levels in model group were (3460.8±105.2)U/L, (2710.4±84.3)U/L and (93.8±1.1)μmol/L, all significantly higher than [(28.1±4.2)U/L,(25.78±2.5)U/L and (3.4±0.4)μmol/L, respectively, P<0.05] in the control, while they all greatly decreased in TDZD-8-intervened group [(370.1±7.1)U/L, (277.3±20.3)U/L and (35.1±0.8)μmol/L, respectively, P<0.05]; the liver homogenate TNF-α, IL-1β and serum cf-DNA levels in the model were (3004.6±239.2)pg/mL, (469.6±56.7)pg/mL and (772.2±192.2) ng/mL, while they all greatly decreased in TDZD-8-intervened group [(2353.3±284.7)pg/mL, (339.2±48.7)pg/mL and (180.0±15.4)ng/mL, respectively, P<0.05]; the hepatic expression of IL-18 and IL-1β in the model intensified greatly as compared to in the control (P<0.05), while they both became weaker in TDZD-8-intervened group (P<0.05); the relative hepatic expression of ULK1 and Beclin1 obviously decreased(P<0.05), and the hepatic expression of P62 protein increased greatly(P<0.05)compared to in the control, while the ULK1 and Beclin1 expression greatly intensified, and the P62 expression became weaker (P<0.05) in TDZD-8-intervened mice. Conclusion The inhibition of GSK3β activity in a mouse model of acute liver failure could protect the liver injuries, which might be related to the up-regulation of autophagy and the inhibition of inflammatory cytokine release.

Key words: Acute liver failure, Glycogen synthase kinase3β, Autophagy, Cytokines