Effect of Chronic Coadministration of Endotoxin and Ethanol on Rat Liver Pathology and Proinflammatory and Anti–Inflammatory Cytokines
Open Access
- 1 May 1999
- journal article
- research article
- Published by Wolters Kluwer Health in Hepatology
- Vol. 29 (5) , 1503-1510
- https://doi.org/10.1002/hep.510290508
Abstract
To better understand how gut–derived endotoxins influence alcohol–induced liver injury and the expression of inflammatory cytokines a new animal model was developed. After 2 weeks on a modified ethanol–containing liquid diet, some rats also were infused with endotoxin via osmotic minipumps for 4 additional weeks. Ethanol diet alone increased plasma endotoxin threefold to 9.3 pg/mL. Endotoxin infusion increased the levels to 388 and 513 pg/mL in controls and ethanol–fed animals, respectively. Panlobular macrovesicular and microvesicular steatosis and inflammatory foci were observed in livers from both ethanol– and ethanol–endotoxin-treated animals, but there was no significant potentiation by endotoxin. Only minor changes, mainly polymorphonuclear infiltration, were seen in animals treated with endotoxin alone although the messenger RNA (mRNA) expression of both proinflammatory cytokines tumor necrosis factor α (TNF–α), interleukin 1β (IL–1β) and anti–inflammatory cytokines IL–4 and IL–10 were markedly increased, as shown by competitive polymerase chain reaction (PCR) analysis using cyclophilin as standard. The effect of endotoxin infusion on cytokine mRNA expression in ethanol–fed animals was not significantly different. Expression of transforming growth factor β1 (TGF–β1 ) mRNA was increased twofold by ethanol, eightfold by endotoxin, but only threefold by ethanol–endotoxin treatment. The mRNA expression of lipopolysaccharide binding protein (LBP) and CD14 endotoxin receptor was not significantly increased by chronic endotoxin treatment, contrasting with the marked elevation observed after acute endotoxin challenge. These results suggest that the tolerance observed despite sustained hepatic expression of proinflammatory cytokines is counteracted by the anti–inflammatory cytokines and by down–regulation of CD14 and LBP. Furthermore, a similar adaptation may occur in alcoholics with continuous endotoxemia.Keywords
Funding Information
- Swedish Alcohol Research Fund, by the Swedish Medical Research Council, and in Finland by the Oscar Öflund Fund and the Mary och Georg Ehrnrooth Fund
This publication has 45 references indexed in Scilit:
- Ethanol feeding enhances inflammatory cytokine expression in lipopolysaccharide-induced hepatitisJournal of Gastroenterology and Hepatology, 1997
- ALCOHOL AND ENDOTOXIN: ANOTHER PATH TO ALCOHOLIC LIVER INJURY?Alcohol, Clinical and Experimental Research, 1995
- CD14 and other recognition molecules for lipopolysaccharide: A reviewImmunopharmacology, 1995
- Inactivation of Kupffer cells prevents early alcohol-induced liver injuryHepatology, 1994
- Lactobacillus Feeding Reduces Endotoxemia and Severity of Experimental Alcoholic Liver (Disease)Experimental Biology and Medicine, 1994
- CD14, a Receptor for Complexes of Lipopolysaccharide (LPS) and LPS Binding ProteinScience, 1990
- Intestinal Endotoxins as Co-Factors in Liver InjuryImmunological Investigations, 1989
- Endotoxin induced hepatic necrosis in rats on an alcohol dietThe Journal of Pathology, 1987
- Endotoxemia in patients with alcoholic and non-alcoholic cirrhosis and in subjects with no evidence of chronic liver disease following acute alcohol excessJournal of Hepatology, 1987
- THE LEAKY GUT OF ALCOHOLISM: POSSIBLE ROUTE OF ENTRY FOR TOXIC COMPOUNDSPublished by Elsevier ,1984