TY - JOUR
T1 - The effect of a fish oil enriched diet on oxygen toxicity and lipid peroxidation in mice
AU - Burns, Alex
AU - Yiguang, Lin
AU - Gibson, Robert
AU - Jamieson, Dana
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1991/9/12
Y1 - 1991/9/12
N2 - Mice were fed a chow diet or diets enriched in fish oil, sunflower oil or beef tallow for 3 weeks. Fatty acid analysis was carried out in samples of plasma, brain and lungs from these animals and large changes were found in plasma and lungs with relatively small dietary-induced changes in brain tissue. Bleeding times were increased very significantly in the fish oil group, and slightly increased in the sunflower oil group. Endogenous lipid peroxidation (measured as thiobarbituric acid reactive substances) was unchanged in lung and brain, but lung tissue from fish oil fed mice produced more lipid peroxides in vitro during incubation at 37° than those of other dietary groups. Mice fed the four different diets were exposed to hyperbaric oxygen at 618, 585 and 515 kPa and convulsive activity and lung damage was recorded. No dietary-induced alterations in susceptibility to oxygen toxicity were found.
AB - Mice were fed a chow diet or diets enriched in fish oil, sunflower oil or beef tallow for 3 weeks. Fatty acid analysis was carried out in samples of plasma, brain and lungs from these animals and large changes were found in plasma and lungs with relatively small dietary-induced changes in brain tissue. Bleeding times were increased very significantly in the fish oil group, and slightly increased in the sunflower oil group. Endogenous lipid peroxidation (measured as thiobarbituric acid reactive substances) was unchanged in lung and brain, but lung tissue from fish oil fed mice produced more lipid peroxides in vitro during incubation at 37° than those of other dietary groups. Mice fed the four different diets were exposed to hyperbaric oxygen at 618, 585 and 515 kPa and convulsive activity and lung damage was recorded. No dietary-induced alterations in susceptibility to oxygen toxicity were found.
UR - https://www.scopus.com/pages/publications/0025775610
U2 - 10.1016/0006-2952(91)90445-B
DO - 10.1016/0006-2952(91)90445-B
M3 - Article
C2 - 1930258
AN - SCOPUS:0025775610
SN - 0006-2952
VL - 42
SP - 1353
EP - 1360
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 7
ER -