Dietary comparison of conjugated linolenic acid (9 cis, 11 trans, 13 trans) and α-tocopherol effects on blood lipids and lipid peroxidation in alloxan-induced diabetes mellitus in rats

被引:29
作者
Dhar, P [1 ]
Bhattacharyya, DK [1 ]
Ghosh, S [1 ]
机构
[1] Univ Calcutta, Coll Sci & Technol, Dept Chem Technol, Kolkata, India
关键词
D O I
10.1007/s11745-006-5069-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present study investigated the dietary effect of conjugated linolenic acid (CLnA) on lipid profiles and lipid peroxidations in alloxan-induced diabetes mellitus in rats. Diabetic rats were fed with 20% sunflower oil (diabetic control), sunflower oil supplemented with 0.5% CLnA, sunflower oil supplemented with 0.159% alpha-tocopherol, and sunflower oil containing 0.25% CLnA + 0.1511% alpha-tocopherol. The results demonstrated that 0.5% CLnA, 0.15% alpha-tocopherol, and 0.25% CLnA + 0.15% alpha-tocopherol each on supplementation significantly lowered total cholesterol and non-HDL-cholesterol in comparison with the diabetic control group. The TAG level was significantly lowered in both the 0.150% alpha-tocopherol and 0.25% CLnA + 0.15% alpha-tocopherol groups. LDL-lipid peroxidation and erythrocyte membrane lipid peroxidation were reduced significantly in each of the experimental groups vs. the control group. The CLnA + alpha-tocopherol diet induced a greater reduction in membrane lipid and liver lipid peroxidation than the alpha-tocopherol diet alone. In conclusion, dietary CLnA exerts antioxidant activity as evidenced by reduced lipid peroxidation in chemically induced diabetes mellitus.
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页码:49 / 54
页数:6
相关论文
共 34 条
[31]   STREPTOZOCIN-INDUCED AND ALLOXAN-INDUCED H2O2 GENERATION AND DNA FRAGMENTATION IN PANCREATIC-ISLETS - H2O2 AS MEDIATOR FOR DNA FRAGMENTATION [J].
TAKASU, N ;
KOMIYA, I ;
ASAWA, T ;
NAGASAWA, Y ;
YAMADA, T .
DIABETES, 1991, 40 (09) :1141-1145
[32]  
WARNICK GR, 1985, CLIN CHEM, V31, P217
[33]  
Wills ED, 1987, BIOCH TOXICOLOGY PRA
[34]   DIABETES-MELLITUS AND FREE-RADICALS [J].
WOLFF, SP .
BRITISH MEDICAL BULLETIN, 1993, 49 (03) :642-652