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Journal of Nutrition Vol. 94 No. 2 February 1968, pp. 237-242
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Availability of Vitamin B6 Vitamers Fed Orally to Long-Evans Rats as Determined by Tissue Transaminase Activity and Vitamin B6 Assay1, 2,

V. F. Thiele and M. Brin

Department of Nutrition and Food Science, Syracuse University, Syracuse, New York; Upstate Medical Center, State University of New York, Syracuse, New York

To study 1) the availability of the 3 vitamin B6-vitamers when fed orally, and 2) the relationships between the vitamin B6-vitamer content of rat tissues to glutamic-pyruvic and glutamic-oxaloacetic transaminase activity, 8 groups of weanling rats of the Long-Evans strain were fed a vitamin B6-deficient diet for 14 days with the following modifications: group 1, no supplement; groups 2, 3, 4, 5 µg of pyridoxal, pyridoxol and pyridoxamine, respectively (administered daily as oral supplements); groups 5, 6, 7, 15 µg of pyridoxal, pyridoxol and pyridoxamine, respectively (administered daily as oral supplements); and group 8, 4 µg of pyridoxol/g of diet. Generally the total vitamin B6 and the 3 vitamer levels of the tissues (liver, kidney, brain, muscle and heart) from rats receiving the 15-µg supplements were higher than those receiving the 5-µg vitamer supplements. This same effect was observed with glutamic-pyruvic transaminase and glutamic-oxaloacetic transaminase enzyme activity. However, no great differences were observed either in tissue vitamer content or enzyme activity due to the form of the vitamer fed. Thus the data indicated that, when fed orally, the 3 vitamers were equally available to the rat. The rat tissues were more severely depleted of pyridoxol than the other 2 vitamers. The extent of tissue depletion of pyridoxamine was similar to the depletion of total vitamin B6 content. Glutamic-pyruvic transaminase was depleted to a greater extent than glutamic-oxaloacetic transaminase.


1 This study was aided by Public Health Service Research grants no. AM-09540 and AM-03127 from the National Institute of Arthritis and Metabolic Diseases.

2 Presented in part at the annual meeting of the Federation of American Societies for Experimental Biology, Chicago, 1967.

Manuscript received 24 August 1967.





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