MODULATION OF PLASMA AND HEPATIC OXIDATIVE STATUS AND CHANGES IN PLASMA-LIPID PROFILE BY N-3 (EPA AND DHA), N-6 (CORN-OIL) AND A 3-THIA FATTY-ACID IN RATS
A. Demoz et al., MODULATION OF PLASMA AND HEPATIC OXIDATIVE STATUS AND CHANGES IN PLASMA-LIPID PROFILE BY N-3 (EPA AND DHA), N-6 (CORN-OIL) AND A 3-THIA FATTY-ACID IN RATS, Biochimica et biophysica acta (G). General subjects, 1199(3), 1994, pp. 238-244
This manuscript describes changes in plasma lipid profiles and paramet
ers of oxidative status in the plasma and liver of rats fed 5 differen
t fatty acids: 95% eicosapentaenoic acid, 92% docosahexaenoic acid (DH
A), corn oil (n-6), 1-mono-(carboxymethylthio)-tetradecane (CMTTD) and
palmitic acid (controls) for 3 months. At the given doses both EPA an
d the 3-thia fatty acid, CMTTD, caused a significant decrease in plasm
a triglycerides, phospholipids, free fatty acids and cholesterol. DHA
decreased plasma free fatty acids and cholesterol, while corn oil feed
ing reduced only plasma free fatty acids. Plasma and hepatic vitamin E
levels were significantly decreased in EPA, DHA and CMTTD fed rats, b
ut remained unchanged in corn oil fed rats. Plasma glutathione was not
ed to decrease after EPA and DHA feeding but remained unchanged in oth
er groups. However, hepatic glutathione content was increased in EPA,
DHA and CMTTD fed rats, whereas cysteine levels were noted to decrease
. As hepatic levels of cysteinylglycine remained unchanged, increased
rate of cellular glutathione synthesis rather than its decreased degra
dation is likely to contribute to the increased hepatic glutathione co
ntent in EPA, DHA and CMTTD fed rats. Except for reduction in the leve
ls of plasma lipid peroxidation caused by CMTTD, no significant change
s were noted between the different treatment groups. Hepatic lipid per
oxidation was elevated only in rats given DHA. Furthermore, our result
s show that EPA and DHA cause minimal imbalance of the peroxisomal H2O
2 metabolising enzymes as compared to CMTTD. In addition, contrary to
the potent peroxisome proliferator compound CMTTD which decreased the
activities of glutathione transferase and glutathione peroxidase, EPA
and DHA increased the activities of these detoxification enzymes.