Effects of Longdan Xiegan Pill on Expression of Multidrug Resistance Protein and Neutrophil CD18 in Cholestatic Rats
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Effects of Longdan Xiegan Pill on Expression of Multidrug Resistance Protein and Neutrophil CD18 in Cholestatic Rats
Chinese Journal of Experimental Traditional Medical FormulaeVol. 17, Issue 21, Pages: 214-217(2011)
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Published:2011
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DONG Wei, LIANG Ai-hua, LI Chun-ying, et al. Effects of Longdan Xiegan Pill on Expression of Multidrug Resistance Protein and Neutrophil CD18 in Cholestatic Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(21): 214-217.
DOI:
DONG Wei, LIANG Ai-hua, LI Chun-ying, et al. Effects of Longdan Xiegan Pill on Expression of Multidrug Resistance Protein and Neutrophil CD18 in Cholestatic Rats[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(21): 214-217.DOI:
Effects of Longdan Xiegan Pill on Expression of Multidrug Resistance Protein and Neutrophil CD18 in Cholestatic Rats
Objective: To observe the effect of Longdan Xiegan pill (LD) on expression of multidrug resistance protein and neutrophil CD18 and tclarify the possible mechanism of LD to clear dampness-heat of liver and gallbladder. Method: Twenty healthy Wistar rats were randomly divided into 4 groups:control group
ANIT-treated model group
LD 5.0 g·kg-1group and LD 2.5 g·kg-1group. LD groups were administered orally for 8 days
while control group and model group were administered orally with equal distilled water
once daily. After the last administration for 1 h
model group and LD groups were treated with 100 mg·kg-1 ANIT
while control group was administered with equal peanut oil. After administration of ANIT 72 hours
The liver total RNA of all rats wwas extracted and the levels of MDR1a
MDR1b
MDR2
MRP1 and MRP2 mRNA in liver tissue were detected by reverse transcription polymerase chain reaction (RT-PCR). The expression of CD18 was measured by using flow cytometer. Total leukocytes and granular leukocytes were counted by using microcomputer controlled hematology analyzer. Result: The expression of MDR1a
MDR1b mRNA in model group wwas significantly higher than that of control group (P<0.05
P<0.01). The expression of MDR2
MRP1
MRP2 mRNA was not obviously changed. LD 5.0
2.5 g·kg-1 group had no obvious effects on expression of multidrug resistance protein in cholestatic rats. LD groups could reduce total leukocytes granular leukocytes and CD18 fluorescence intensity. Conclusion: LD has protection in ANIT-induced cholestatic rats
which is similar to the syndrome of dampness-heat of liver and gallbladder. The protection mechanism maybe mainly related to inhibiting endothelial-leukocyte adhesion
inhibiting inflammatory responses in bile ducts
alleviating biliary injuries
increasing bile flow of intrahepatic bile ducts
not related to the expresion of MRP1 and MRP2 mRNA in biliary epithelial cells.