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Vol. 299, Issue 2, 638-644, November 2001
Department of Pathology and Center for the Study of Liver Diseases,
The University of Hong Kong, Hong Kong, China (A.A.N.); Research Unit
of Alcohol Diseases, Helsinki University Central Hospital, Helsinki,
Finland (K.J.); Department of Anatomy, The University of Hong Kong,
Hong Kong, China (G.L.T.); Department of Pathology, Harvard Medical
School, Boston, Massachusetts (A.R.); and Department of Medicine, Weill
Medical College of Cornell University and Anne Fisher Nutrition Center
at Strang Cancer Prevention Center, New York, New York (A.J.D.)
We investigated the potential of dietary saturated fatty acids to
reverse alcoholic liver injury despite continued administration of
alcohol. Five groups (six rats/group) of male Wistar rats were studied.
Rats in groups 1 and 2 were fed a fish oil-ethanol diet for 8 and 6 weeks, respectively. Rats in groups 3 and 4 were fed fish oil and
ethanol for 6 weeks before being switched to isocaloric diets
containing ethanol with palm oil (group 3) or medium-chain triglycerides (MCTs, group 4) for 2 weeks. Rats in group 5 were fed
fish oil and dextrose for 8 weeks. Liver samples were analyzed for
histopathology, lipid peroxidation, nuclear factor-
B (NF-
B) activation, and mRNAs for cyclooxygenase-2 (Cox-2) and tumor necrosis factor-
(TNF-
). Endotoxin in plasma was determined. The most severe inflammation and fibrosis were detected in groups 1 and 2, as
were the highest levels of endotoxin, lipid peroxidation, activation of
NF-
B, and mRNAs for Cox-2 and TNF-
. After the rats were switched
to palm oil or MCT, there was marked histological improvement with
decreased levels of endotoxin and lipid peroxidation, absence of
NF-
B activation, and reduced expression of TNF-
and Cox-2. A diet
enriched in saturated fatty acids effectively reverses alcohol-induced
necrosis, inflammation, and fibrosis despite continued alcohol
consumption. The therapeutic effects of saturated fatty acids may be
explained, at least in part, by reduced endotoxemia and lipid
peroxidation, which in turn result in decreased activation of NF-
B
and reduced levels of TNF-
and Cox-2.
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