We have shown previously that plating primary cultures of rat hepatocytes under low density, which stimulates hepatocytes to shift from the G 0 to the G 1 phase of the cell cycle, resulted in increased levels of glutathione (GSH) and cysteine, and increased activity of β₯-glutamylcysteine synthetase
Hepatic Glutathione Homeostasis in the Rat: Efflux Accounts for Glutathione Turnover
β Scribed by Bernhard H. Lauterburg; James D. Adams; Jerry R. Mitchell
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 553 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0270-9139
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β¦ Synopsis
Hepatic glutathione turnover and the efflux of glutathione from the liver into bile and blood were measured in male Sprague-Dawley rats in uiuo. In fed rats the efflux of glutathione into blood, calculated from the hepatic arteriovenous concentration gradient and hepatic blood flow, amounted to 12.4 f 1.4 nmoles min-gm liver. Together with the excretion of glutathione into bile (3.4 f 0.4 nmoles per min.gm liver) total efflux accounted for the hepatic turnover of glutathione of 15.2 f 0.9 nmoles per min.gm liver. Fasting animals for 48 h r markedly increased hepatic glutathione turnover to 26.4 f 1.2 nmoles per min.gm liver. Increased efflux into blood rather than increased intrahepatic catabolism accounted for this increased turnover. The systemic clearance of glutathione was 3.22 f 0.51 ml per min. 100 gm body weight. The efflux of glutathione from liver therefore was calculated to contribute over 90% of total glutathione inflow into the circulation, as determined from the clearance and the arterial concentration of glutathione. Thus, the liver is the major source of plasma glutathione, and turnover of hepatic glutathione in the basal state is accounted for almost entirely by efflux of glutathione from the liver. During fasting, the plasma clearance of exogenous glutathione increased to 5.32 f 0.35 ml per min.100 gm body
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