Since little is known regarding the etiologic role of the immune system in alcohol-induced liver injury, this proposal represents an attempt to define cellular, humoral, and serum factors which are operative during the disease process. We will compare these studies to other acute and chronic liver diseases to determine if there are unique abnormalities attributable to patients with alcoholic liver disease. We have demonstrated the presence of circulating immune complexes in patients with acute alcoholic hepatitis and now will examine their physical properties and antigenic composition. The search for tissue deposition in the liver is of critical importance. There are potent circulating inhibitory factors in the serum of patients with alcoholic hepatitis which dramatically influence the effector function of normal cells and we will further explore their physical-chemical properties and biological activity on autologous lymphocytes. Investigations will be initiated to examine the control of immunoglobulin synthesis in vitro which may provide new and important information on the mechanism(s) of hypergammaglobulinemia so often observed in these patients. Finally, we will study the effect(s) of acute and chronic ethanol intoxication on hepatic regeneration. In this regard both in vivo and in vitro systems will be employed to probe the control of DNA synthesis and the possible mechanisms of ethanol action on liver repair. Thus, one of the long-term goals of this research is to focus on the magnitude and rate of liver repair under experimental conditions. It is reasonable to suspect that ethanol may have similar inhibitory effects on the hepatocyte proliferation response in man.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA002666-09
Application #
3108792
Study Section
Alcohol Biomedical Research Review Committee (ALCB)
Project Start
1979-07-01
Project End
1989-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
9
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
Derdak, Zoltan; Villegas, Kristine A; Wands, Jack R (2012) Early growth response-1 transcription factor promotes hepatic fibrosis and steatosis in long-term ethanol-fed Long-Evans rats. Liver Int 32:761-70
de la Monte, Suzanne; Derdak, Zoltan; Wands, Jack R (2012) Alcohol, insulin resistance and the liver-brain axis. J Gastroenterol Hepatol 27 Suppl 2:33-41
de la Monte, Suzanne M; Pang, Maoyin; Chaudhry, Rajeev et al. (2011) Peroxisome proliferator-activated receptor agonist treatment of alcohol-induced hepatic insulin resistance. Hepatol Res 41:386-98
Derdak, Zoltan; Lang, Charles H; Villegas, Kristine A et al. (2011) Activation of p53 enhances apoptosis and insulin resistance in a rat model of alcoholic liver disease. J Hepatol 54:164-72
de la Monte, Suzanne M; Wands, Jack R (2010) Role of central nervous system insulin resistance in fetal alcohol spectrum disorders. J Popul Ther Clin Pharmacol 17:e390-404
He, Jiman; de la Monte, Suzanne; Wands, Jack R (2010) The p85beta regulatory subunit of PI3K serves as a substrate for PTEN protein phosphatase activity during insulin mediated signaling. Biochem Biophys Res Commun 397:513-9
Szabo, Gyongyi; Wands, Jack R; Eken, Ahmet et al. (2010) Alcohol and hepatitis C virus--interactions in immune dysfunctions and liver damage. Alcohol Clin Exp Res 34:1675-86
Siu, Larry; Foont, Julie; Wands, Jack R (2009) Hepatitis C virus and alcohol. Semin Liver Dis 29:188-99
de la Monte, Suzanne M; Longato, Lisa; Tong, Ming et al. (2009) Insulin resistance and neurodegeneration: roles of obesity, type 2 diabetes mellitus and non-alcoholic steatohepatitis. Curr Opin Investig Drugs 10:1049-60
de la Monte, Suzanne M; Tong, Ming (2009) Mechanisms of nitrosamine-mediated neurodegeneration: potential relevance to sporadic Alzheimer's disease. J Alzheimers Dis 17:817-25

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