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-Tocopherol1



2
Departments of
*
Nutrition and Dietetics and
Clinical Biochemistry, Kings College, London, UK
2To whom correspondence should be addressed.
Some studies have shown that reductions in tissue protein synthesis,
under a variety of cytotoxic conditions, are ameliorated by
-tocopherol (ATC) supplementation. We have also shown evidence of
increased oxidative stress and reduced protein synthesis rates in
alcohol-exposed muscle. Serum levels of ATC fall and rates of
muscle protein synthesis are reduced in patients with alcoholic
myopathy. We therefore tested the hypothesis that treatment with ATC
could ameliorate the ethanol-induced changes in muscle protein
synthesis, a contributory event in the pathogenesis of alcoholic muscle
disease. Studies were carried out on gastrocnemius (Type II
fiber-predominant and usually considered representative of the
musculature as a whole), soleus (Type I fiber-predominant) and
plantaris (Type II fiber-predominant) muscles. For comparative
purposes, we also investigated the liver. Young male Wistar rats (90 g
body weight) were injected intraperitoneally (i.p.) daily with ATC (30
mg/kg body weight) in Intralipid fat emulsion (0.1 mL/100 g body, i.p.)
for 5 d. Controls were similarly injected with the Intralipid
vehicle alone. After ATC supplementation, rats were given ethanol (75
mmol/kg body weight, i.p., 2.5 h) or saline (0.15 mol/L NaCl,
i.p.). Fractional rates of tissue protein synthesis (i.e., the
percentage of the tissue protein pool renewed each day,
ks, %/d) and RNA activities [i.e., the
amount of protein synthesis each day per unit RNA,
kRNA, mg protein/d/mg RNA)] were then
measured. Supplementation increased ATC concentrations in plasma,
gastrocnemius and liver. There was no effect of ATC supplementation
alone on ks in any of the tissues. ATC
supplementation in the absence of alcohol increased
kRNA in the plantaris muscle. In
nonsupplemented groups, acute ethanol treatment reduced skeletal muscle
(soleus, plantaris and gastrocnemius) ks.
Hepatic ks was not altered by ethanol,
although ATC concentrations in this tissue increased due to ethanol.
However, none of the changes in muscle ks or
kRNA due to ethanol were significantly
affected by ATC supplementation. In conclusion, ATC supplementation
does not appear beneficial in ameliorating acute alcohol toxicity in
skeletal muscle as defined by reductions in protein synthesis.
KEY WORDS:
-tocopherol muscle liver protein synthesis rats alcohol
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