scholarly journals Coagulative and Fibrinolytic Activities in Primary Cultured Rat Hepatocytes Treated with Carbon Tetrachloride

1993 ◽  
Vol 5 (1) ◽  
pp. 51-62
Author(s):  
Hironori KATOH ◽  
Mayumi TSUJI ◽  
Masako OKAZAKI ◽  
Katsuji OGUCHI
1989 ◽  
Vol 24 (4) ◽  
pp. 447-447
Author(s):  
H. Yamamoto ◽  
Y. Kondo ◽  
T. Kawabe ◽  
K. Okano ◽  
R. Sassa ◽  
...  

2010 ◽  
Vol 38 (06) ◽  
pp. 1193-1205 ◽  
Author(s):  
H.M. Chi ◽  
S.T. Chou ◽  
S.C. Lin ◽  
Z.Y. Su ◽  
Lee-Yan Sheen

The objective of this study was to investigate the effects of various concentrations and incubation times of water extract of clam (WEC) on glutathione, its antioxidant and the detoxification defense systems in normal and CCl4 -induced oxidative damaged primary rat hepatocytes. This study showed that when the hepatocytes were treated with WEC(0.14 ~ 1.68 mg/ml), the intracellular glutathione (GSH) levels, GSH/GSSG ratio, and the activities of GSH-related enzymes (GPx, GRd, and GST) were higher than those in the control at 24 or 48 hour treatments. However, the lactate dehydrogenase (LDH) leakage and microscopic observations did not differ from those of the control. Yet, when the hepatocytes were pretreated with various concentrations of WEC for 24 hours and then exposed to 5 mM carbon tetrachloride (CCl4) for 1 hour, at concentrations of WEC between 0.42 ~ 1.68 mg/ml, the viabilities, intracellular GSH level, and activities of GST and GPx were significantly increased compared to those of the CCl4 -treated control group ( p < 0.05). In conclusion, WEC could improve the viability and the capabilities of detoxification and antioxidation in hepatocytes by increasing the GSH level and the activities of GSH-related enzymes.


1991 ◽  
Vol 19 (2) ◽  
pp. 209-213
Author(s):  
Gabi Schepers ◽  
Christiane Aschmann ◽  
Sabine Mörchel

An in vitro test protocol is reported, which, using primary cultured rat hepatocytes, allows for the screening of xenobiotic effects on biotransformation as well as on basal cellular functions. O-Deethylation of 7-ethoxycoumarin (7-EC) and subsequent conjugation of the metabolite 7-hydroxycoumarin (7-HC) with sulphate or glucuronic acid are determined, as representative parameters for the hepatic biotransformation. Cell viability is examined by measuring cellular ATP content and leakage of lactate dehydrogenase. With respect to immediate and delayed effects on biotransformation reactions, the standard test protocol includes exposure to xenobiotics for 1, 24 and 48 hours. Different response patterns could be demonstrated for the solvents dimethylformamide (DMF) and dimethylsulphoxide (DMSO), and the chlorinated phenols, pentachlorophenol (PCP) and hexachlorophene (HCP), which are known to uncouple mitochondrial respiration. Short-term incubation with the solvents resulted in decreased 7-EC- O-deethylation without signs of cytotoxicity. PCP and HCP inhibited 7-EC- O-deethylation and 7-HC-conjugation, affecting sulphate and glucuronide formation differently. 24-hour exposures to PCP and HCP resulted in decreased 7-ethoxycoumarin- O-deethylase activity, which correlated with diminished cell viability, while DMSO and DMF enhanced 7-EC- O-deethylation at sub-cytotoxic concentrations. After exposure for 48 hours to the solvents, enzyme induction was even more pronounced.


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