Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-29T04:36:41.175Z Has data issue: false hasContentIssue false

Abnormal essential fatty acid composition of tissue lipids in genetically diabetic mice is partially corrected by dietary linoleic and γ-linolenic acids

Published online by Cambridge University Press:  24 July 2007

S. C. Cunnane
Affiliation:
Efamol Research Institute, PO Box 818, Kentville, Nova Scotia, CanadaB4N 4H8
M. S. Manku
Affiliation:
Efamol Research Institute, PO Box 818, Kentville, Nova Scotia, CanadaB4N 4H8
D. F. Horrobin
Affiliation:
Efamol Research Institute, PO Box 818, Kentville, Nova Scotia, CanadaB4N 4H8
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

1. Genetically diabetic mice (db/db)and their non-diabetic litter-mates were maintained for 15 weeks on diets supplemented with safflower oil or evening primrose (Oenothera bienis) oil, both essential fatty acid (EFA)-rich sources, or hydrogenated coconut oil (devoid of EFA).

2. Plasma glucose was higher in the diabetic mice supplemented with the oils than in the unsupplemented diabetic mice. In the oil-supplemented non-diabetic mice, plasma glucose did not differ compared with the unsupplemented non-diabetic mice.

3. The proportional content of arachidonic acid in the phospholipids of the pancreas was significantly decreased in diabetic mice, an effect which was completely prevented by supplementation with safflower or evening primrose oil but not hydrogenated coconut oil.

4. In the liver phospholipids of the diabetic mice, dihomo-γ-linolenic acid was proportionally increased, an effect reduced by supplementation with safflower oil but not evening primrose or hydrogenated coconut oils.

5. In the liver triglycerides of the diabetic mice, γ-linolenic acid, dihomo-γ-linolenic acid and arachidonic acid were all proportionally decreased, effects which were also prevented by safflower or evening primrose oil but not hydrogenated coconut oil.

6. Alopecia and dry scaly skin were prominent in the diabetic mice but less extensive in the diabetic mice supplemented with EFA.

Type
Papers of direct relevance to Clinical and Human Nutrition
Copyright
Copyright © The Nutrition Society 1985

References

Brenner, R. R. (1977). Advances in Experimental Biology and Medicine 83, 85102.CrossRefGoogle Scholar
Brenner, R. R., Peluffo, R. O., Mercuri, O. &Restelli, M. A. (1968). American Journal of Physiology 215, 6369.Google Scholar
Clark, D. L., Hamel, F. G. &Queener, S. F. (1983). Lipids 18, 696705.Google Scholar
Coleman, D. L. (1981). In Mammalian Genetics and Cancer: The Jackson Laboratory Fiftieth Anniversary Symposium, pp. 145158. New York: A. R. Liss.Google Scholar
Coleman, D. L. &Hummel, K. P. (1967). Diabetologia 3, 238248.Google Scholar
Cunnane, S. C., Manku, M. S. & Horrobin, D. F. (1985). British Journal of Nutrition. 53, 441448.Google Scholar
De Alaniz, M. J. T. & Brenner, R. R. (1969). Acta Physiologica Latinoamericana 19, 115.Google Scholar
Faas, F. H. & Carter, W. J. (1980).Lipids 15, 953961.Google Scholar
Faas, F. H. & Carter, W. J. (1983).Lipids 18, 339342.Google Scholar
Futterman, S. & Kupfer, C. (1968). Investigative Ophthalmology 7, 105108.Google Scholar
Holman, R. T., Johnson, S. B., Gerrard, J. M., Mauer, S. M., Kupcho-sandberg, S. & Brown, D. M. (1983). Proceedings of the National Academy of Science, USA 80, 23752379.Google Scholar
Houtsmuller, A. J., van Hal-Ferwerda, J., Zahn, K. J. & Henkes, H. E. (1980). Nutrition and Metabolism 24 (Suppl.1), 105108.Google Scholar
Houtsmuller, A. J., van Hal-Ferwerda, J., Zahn, K. J. & Henkes, H. E. (1981). Progress in Lipid Research 20, 377386.Google Scholar
Huang, Y.-S., Horrobin, D. F., Manku, M. S., Mitchell, J. & Ryan, M. A. (1984). Lipids 19, 367370.Google Scholar
Jones, D. B., Carter, R. D., Haitas, B. & Mann, J. I. (1983). British Medical Journal 286, 173175.Google Scholar
Laychock, S. (1983). Diabetes 32, 613.Google Scholar
Mercuri, O., Peluffo, R. O. & Brenner, R. R. (1966). Biochimica et Biophysica Acta 116, 406411.Google Scholar
Poisson, J. P., LeMarchal, P., Blond, J. P., Lecerf, J. & Mendy, F. (1978). Diabetes and Metabolism 4, 3945.Google Scholar
Pratt, J. D. (1984). Hormone and Metabolic Research 16, 152153.Google Scholar