MA Rong, LI Mao-xing, JIA Zheng-ping, et al. Hepatoprotective Effects of 50% Ethanol Elute of by Macroporous Adsorptive Resins on CCl-induced Acute Liver Injury[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(4): 132-136.
DOI:
MA Rong, LI Mao-xing, JIA Zheng-ping, et al. Hepatoprotective Effects of 50% Ethanol Elute of by Macroporous Adsorptive Resins on CCl-induced Acute Liver Injury[J]. Chinese journal of experimental traditional medical formulae, 2016, 22(4): 132-136. DOI: 10.13422/j.cnki.syfjx.2016040132.
Hepatoprotective Effects of 50% Ethanol Elute of by Macroporous Adsorptive Resins on CCl-induced Acute Liver Injury
Objective: To explore the hepatoprotective effects and the possible mechanism of 50% ethanol elute of Phlomis younghunsbandii by macroporous adsorptive resins (EPY-50) on CCl4-induced acute liver injury rats. Method: Sixty Wistar rats were randomly divided into normal group
model group
bifendate group (bifendate dropping pill
100 mg · kg-1) and EPY-50 high-dose
medium-dose and low-dose (400
200
50 mg · kg-1) groups
continuous for 4 days by gavage. The rats in normal group and model group were given with distilled water. 1 hour after administration on day 3
rats were ip injected with 15% CCl4 olive oil;rats in normal group were ip injected with with olive oil
After contamination for 2 h and 22 h
all groups were administered again and blood was taken from orbital vein at 1 h after the last administration. The levels of serum aspartate aminotransferase (AST)
alanine aminotransferase (ALT)
malondialdehyde (MDA)
and superoxide dismutase (SOD) were detected
then the rats were sacrificed for and livers were taken. The liver index and MDA
SOD
and glutathione reductase (GSH) levels in the liver tissues;in addition
histopathological examination was also done for the livers. Result: Compared with the normal group
serum AST and ALT levels were significantly elevated in model group (P<0.01)
MDA levels were significantly increased (P<0.05)
SOD and GSH levels were statistically reduced in the liver tissues (P<0.05)
the liver index was significantly increased (P<0.01)
indicating that the model of CCl4 injection was successful. Compared with the model group
EPY-50 with high-dose
and medium-dose (400
200 mg · kg-1) could significantly decrease the levels of AST
ALT (P<0.01
P<0.01)
significantly decrease MDA level
increase the SOD and GSH levels
reduce liver index and improve pathological state of the liver tissues. Conclusion: EPY-50 has hepatoprotective effects on CCl4-induced acute liver injury
and the mechanism may be associated with its antioxidative activity.