1.Glucose-6-phosphatase Activity and Ultrastructures in Hepatocytes of Thioacetamide-treated Mice.
Tai Sun SHIN ; Yong Kun DEUNG ; Soo Sung KIM
Yonsei Medical Journal 1976;17(2):85-96
To investigate the earlier cellular alterations(Glucose-6-Pase activity and morphologic features) caused by a hepatotoxin, thioacetamide (TAA), a single dose of the agent (200mg per kg of body weight) was given intraperitoneally to mice, which were sacrificed at intervals of 4, 8 or 16 hours after corresponding treatments. For histochemical study of glucose-6-phosphatase (G6Pase) activity, unfixed frozen sections were incubation of the Wachstein and Meisel medium and stained. The smallest pieces of liver tissue were fixed in glutaraldehyde and osmic acid, and stained by the routine electron-microscopic techniques. Some pieces of liver were fixed in 10% formalin, embedded in paraffin, and stained with hematoxylin and eosin. There was a rapid and progressive loss of G6Pase activity, in an orderly time sequence, in the experimental group. There were also morphologic changes: loss of cytoplasmic basophilia, cell infiltration and necrosis in the centrilobular and intermediate zones, and an increase of sER, small vesicles and ribosomes in the cytoplasm of hepatocytes, the marked changes of nuclei and nucleoli, and a slight increase of lipid droplets in the cytoplasm at 16 hours after intoxication. The correlation between these cellular alterations was discussed in view of mechanisms in the hepatotoxic action.
Acetamides/adverse effects*
;
Animal
;
Glucose-6-Phosphatase/metabolism*
;
Liver/drug effects*
;
Liver/enzymology
;
Liver/ultrastructure
;
Male
;
Mice
;
Thioacetamide/adverse effects*
;
MH -
;
Substances:
;
Acetamides
;
Thioacetamide
;
Glucose-6-Phosphatase
2.Glucose-6-phosphatase Activity and Ultrastructures in Hepatocytes of Thioacetamide-treated Mice.
Tai Sun SHIN ; Yong Kun DEUNG ; Soo Sung KIM
Yonsei Medical Journal 1976;17(2):85-96
To investigate the earlier cellular alterations(Glucose-6-Pase activity and morphologic features) caused by a hepatotoxin, thioacetamide (TAA), a single dose of the agent (200mg per kg of body weight) was given intraperitoneally to mice, which were sacrificed at intervals of 4, 8 or 16 hours after corresponding treatments. For histochemical study of glucose-6-phosphatase (G6Pase) activity, unfixed frozen sections were incubation of the Wachstein and Meisel medium and stained. The smallest pieces of liver tissue were fixed in glutaraldehyde and osmic acid, and stained by the routine electron-microscopic techniques. Some pieces of liver were fixed in 10% formalin, embedded in paraffin, and stained with hematoxylin and eosin. There was a rapid and progressive loss of G6Pase activity, in an orderly time sequence, in the experimental group. There were also morphologic changes: loss of cytoplasmic basophilia, cell infiltration and necrosis in the centrilobular and intermediate zones, and an increase of sER, small vesicles and ribosomes in the cytoplasm of hepatocytes, the marked changes of nuclei and nucleoli, and a slight increase of lipid droplets in the cytoplasm at 16 hours after intoxication. The correlation between these cellular alterations was discussed in view of mechanisms in the hepatotoxic action.
Acetamides/adverse effects*
;
Animal
;
Glucose-6-Phosphatase/metabolism*
;
Liver/drug effects*
;
Liver/enzymology
;
Liver/ultrastructure
;
Male
;
Mice
;
Thioacetamide/adverse effects*
;
MH -
;
Substances:
;
Acetamides
;
Thioacetamide
;
Glucose-6-Phosphatase
3.Reversing effects of silybin on TAA-induced hepatic CYP3A dysfunction through PXR regulation.
Yuan XIE ; Hai-Ping HAO ; Hong WANG ; Zhao-Xian WANG ; Guang-Ji WANG
Chinese Journal of Natural Medicines (English Ed.) 2013;11(6):645-652
AIM:
Silybin (SB), a major constituent of the milk thistle, has been used to treat several liver disorders. However, liver diseases were always accompanied by CYP450 dysfunction. This study was designed to explore the relationship between the hepatoprotective effect and CYP3A regulation of SB during thioacetamide (TAA)-induced rat liver injury.
METHODS:
Serum biochemical analysis and histopathological study were taken to evaluate the hepatoprotectinve effect of SB. α-SMA were detected by immunohistochemical analysis and cytokine release in rat liver was determined by ELISA assay. CYP3A and PXR expression were determined by RT-PCR and Western blot analysis, and CYP3A activity was based on the midazolam 4-hydroxylation reaction. Also, siRNA transfection was induced in HepG2 cells to evaluate the effect of PXR on cytotoxicity and CYP3A4 dysregulation caused by TAA.
RESULTS:
SB showed powerful hepatoprotective effects, and anti-inflammatory and anti-fibrosis effects, and reversed the loss of CYP3A and PXR in TAA-injured rat liver, and decreased PXR translocation into the cell nucleus. PXR silencing weakened the effect of SB on cytoprotection and CYP3A regulation.
CONCLUSIONS
PXR was a very important factor of CYP3A regulation and might be the target of SB in TAA-induced liver disease. Also, because of the potential interactions of SB and co-administered medicines, it might be necessary to adjust the dosage in the clinical medication of liver disease.
Animals
;
Chemical and Drug Induced Liver Injury
;
drug therapy
;
enzymology
;
Cytochrome P-450 CYP3A
;
genetics
;
metabolism
;
Drugs, Chinese Herbal
;
administration & dosage
;
Liver
;
drug effects
;
enzymology
;
metabolism
;
Male
;
Milk Thistle
;
chemistry
;
Pregnane X Receptor
;
Rats
;
Rats, Sprague-Dawley
;
Receptors, Steroid
;
genetics
;
metabolism
;
Signal Transduction
;
drug effects
;
Silybin
;
Silymarin
;
administration & dosage
;
Thioacetamide
;
adverse effects
4.Protective effect of aqueous extract of Feronia elephantum correa leaves on thioacetamide induced liver necrosis in diabetic rats.
Prashant SHARMA ; Subhash L BODHANKAR ; Prasad A THAKURDESAI
Asian Pacific Journal of Tropical Biomedicine 2012;2(9):691-695
OBJECTIVETo evalueate hepatoprotective effects Feronia elephantum (F. elephantum) correa against thioacetamide (TA) induced liver necrosis in diabetic rats.
METHODSMale wistar rats were made diabetic with alloxan (160 mg/kg) on day 0 of the study. They were intoxicated with hepatotoxicant (thioacetamide, 300 mg/kg, ip) on day 9 of study to produce liver necrosis. Effects of 7 day daily once administration (day 2 to day 9) of EF (400 and 800 mg/kg, po) were evaluated on necorosis of liver in terms of mortality, liver volume, liver weight, serum aspartate aminotransferase (AST) and serum alanine transaminase (ALT), and histopathology of liver sections (for signs of necorosis and inflammation) on day-9 of the study. Separate groups of rats with treated only with alloxan (DA control), thioacetamide (TA control) and both (TA+DA control) were maintained.
RESULTSFE significantly lowered the mortality rate and showed improvement in liver function parameters in TA-induced diabetic rats without change in liver weight, volume and serum glucose levels.
CONCLUSIONSFE showed promising activity against TA-induced liver necorsis in diabetic rats and so might be useful for prevention of liver complications in DM.
Animals ; Blood Glucose ; drug effects ; Chemical and Drug Induced Liver Injury ; drug therapy ; mortality ; pathology ; prevention & control ; Diabetes Mellitus, Experimental ; Disease Models, Animal ; Liver Function Tests ; Male ; Necrosis ; Plant Extracts ; administration & dosage ; chemistry ; pharmacology ; Protective Agents ; Rats ; Rutaceae ; chemistry ; Thioacetamide ; adverse effects