WANG Jing-hui, TANG Dong-xin, HUANG Hui, et al. Effect of Gehua Jiecheng Fang on Protein Expression Level of Telomerase in Orthotopic Allograft HCC Mice[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(24): 73-78.
DOI:
WANG Jing-hui, TANG Dong-xin, HUANG Hui, et al. Effect of Gehua Jiecheng Fang on Protein Expression Level of Telomerase in Orthotopic Allograft HCC Mice[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(24): 73-78. DOI: 10.13422/j.cnki.syfjx.2015240073.
Effect of Gehua Jiecheng Fang on Protein Expression Level of Telomerase in Orthotopic Allograft HCC Mice
Objective: To investigate the influence of Gehua Jiecheng Fang(GJF) on the hepatic protein expression level of telomerase in mice. Method: The totally 32 Balb/C mice were randomly divided into the normal group(normal saline)
the model group(normal saline)
the low-and high-dose GJF groups(20
40 g·kg-1) of 8 mice each. The orthotopic allograft hepatic cellular cancer(HCC) model of H22 ascites tumor cells was established. The general observation including the general growth in mice
weight
liver index was conducted the pathological changes of the left hepatic lobe was observes by using HE staining. The changes of alanine aminotransferase(ALT)
aspartate aminotransferase(AST)
glutamyltransferase(GGT) were detected by using ELISA. The protein expression level of telomerase in hepatic tissues was detected by using Western blot. Result: Compared with the normal group
the weight decreased
liver index and the levels of ALT
AST
GGT and protein expression of telomerase increased in the model group(P<0.05). Compared with the model group
the weight increased
liver index and the levels of ALT
AST
GGT and protein expression of telomerase decreased in the low-and high-dose GJF groups(P<0.05). Hepatic tissue and cellular heteromorphism were obvious in the model mice and the damages were reduced in the GJF groups. Conclusion: GJF has certain effect on HCC model by reducing the liver damage
protecting the liver function
regulating the protein expression level of telomerase in mice and restraining the cellular immortalization.