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Influence of fasting‐refeeding and dietary linoleate on liver glucose‐6‐phosphate dehydrogenase and phospholipid fatty acid composition in rats adapted to a purified diet
Author(s) -
Williams M. A.,
Tinoco J.,
Ojakian M. A.,
Clark L.
Publication year - 1977
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/bf02533643
Subject(s) - clinical chemistry , medicine , lipidology , phospholipid , endocrinology , casein , fatty acid , composition (language) , biology , sucrose , chemistry , biochemistry , linguistics , philosophy , membrane
Responses to refeeding after fasting were studied in male rats fed a purified casein‐sucrose diet containing 5% safflower oil. After a 48 hr fast, the rats were fed either the same diet or the same diet minus oil (fat‐free diet). These experiments were designed to distinguish changes due to fasting and refeeding alone without a change of diet from those changes caused by refeeding a diet of different composition. In the first experiment, rats were refed for 3 or 7 days. In rats refed either diet, liver glucose‐6‐phosphate dehydrogenase (G6PD) activity was elevated above refasting levels, but after 7 days, activity in rats refed the 5% safflower oil diet was significantly lower than in those refed the fatfree diet. The amount of liver arachidonate in rats refed the safflower oil diet was the same during refeeding as before fasting. In the second experiment, rats were refed the fat‐free diet for 1, 2, 3, or 7 days. Liver G6PD and fatty acid synthetase were measured, as well as fatty acids in liver total lipids and phospholipids. G6PD activity increased above prefasting levels after one day refeeding and continued to increase, for 7 days. Fatty acid synthetase activity increased for the first 3 days of refeeding, with no additional increase after 7 days. In all rats refed the fat‐free diet, the proportions of arachidonate and linoleate in liver phospholipids diminished with time, and eicosatrienoate appeared. These results show that (a) maintenance of liver phospholipid arachidonate did not prevent increased G6PD activity in early refeeding, but the elevated G6PD activity later declined when phospholipid arachidonate was maintained by feeding a source of linoleate; (b) the metabolic state of fastedrefed rats had not returned to prefasting conditions even after 7 days of refeeding a linoleate‐rich diet to which the rats were adapted before fasting.