JOURNAL OF PRACTICAL HEPATOLOGY ›› 2014, Vol. 17 ›› Issue (2): 168-171.doi: 10.3969/j.issn.1672-5069.2014.02.014

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Tolerance of concanavalin A in three different strains of mice with acute hepatic injury

Yu Huijie, Sheng Guoguang.   

  1. Hubei University of Traditional Chinese Medicine,Wuhan 430065,Hubei Province,China
  • Received:2013-08-01 Online:2014-08-20 Published:2016-04-15

Abstract: Objective To compare the differences in serum liver enzymes, mortality and liver histological changes in three different strains of mice with concanavalin A(ConA) -induced acute hepatic injury (AHI). Methods C57BL/6J mice,BABL/c mice and KM mice were subjected to ConA at four different dosages (i.e.6, 12,20 and 30 mg·kg-1) for 8 hours,and then mice were sacrificed and serum liver enzymes and liver histological changes were examined. Results ConA at dose of 6 mg·kg-1 successfully induced acute liver injury in all three strains of mice;ConA at dose of 12 mg·kg-1 caused remarkable increases in serum ALT (1006.8 ± 12.1) U/L and AST (1391.8 ± 13.4)U/L levels in KM mice,significantly higher than those in BABL/c mice [(75.7 ± 0.5) U/L and (284.7 ± 23.4) U/L,respectively and in C57BL/6J mice (104. ±32.2) U/L and (492.2 ± 12.3) U/L,respectively,P<0.05];Similarly,liver index (5.4±0.3) and spleen index(0.7±0.5) in KM mice were significantly higher than that in BABL/c mice [(5.2±0.4) and (0.6±0.3),respectively and in C57BL/6J mice(5.0±0.6) and (0.6±0.2),respectively,P<0.05];Serum ALT and AST levels did not differ among three strains of mice when Con A at dose of 20 mg·kg-1 was used,however,the mortality in BABL/c (4/10) and C57BL/6J(5/10) was significantly higher than that in KM mice(1/10);30 mg·kg-1 of ConA resulted in a remarkably high mortality in all three strains of mice (30% in KM mice,100% in BABL/c and 100% in C57BL/6J mice). Conclusion Mouse strains play a significant role in liver response to Con A,and the tolerance of KM mice to ConA is better than BABL/c and C57BL/6J mice and the liver damage is in a dose-dependent manner.

Key words: Acute liver injury, Concanavalin A, KM mice, BABL/c mice, C57BL/6J mice