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Journal of Nutrition Vol. 56 No. 1 May 1955, pp. 67-82
Copyright © 1955 by American Society for Nutrition
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The Absorption of Cyanocobalamin1 (Vitamin B12) from the gastrointestinal tract of dogs,2,3,

Four Figures

Harold L. Rosenthal4 and John K. Hampton, Jr.5

Departments of Medicine, Biochemistry and Physiology, Tulane University School of Medicine, New Orleans, Louisiana

In the post-absorptive state, plasma vitamin B12 activity of dogs is the same in portal and peripheral blood plasma, but portal plasma contains greater amounts of activity than does peripheral plasma during active absorption of the vitamin from the intestinal tract.

Crystalline vitamin B12 placed in ligated segments of the duodenum or in the unligated duodenum of dogs results in the rapid appearance of vitamin B12 activity in the plasma of portal and peripheral blood. During absorption, small but definite amounts of vitamin activity also appear in the urine. In dogs subjected to operation but administered saline in place of vitamin B12, plasma and urine activity remained constant. The plasma vitamin B12 activity of dogs with stomachs ligated at the duodenal cap remained essentially constant following the administration of vitamin.

The major portion of vitamin B12 administered by intravenous injection, in an amount approximately that found in plasma during oral absorption, results in a rapid elimination of the vitamin in the urine. These data are discussed in relation to the problem of vitamin B12 absorption in man and animals.


1 Cyanocobalamin is used to designate crystalline vitamin B12 in this report. The term "vitamin B12 activity" denotes all substances representing such activity for Lactobacillus leichmanii. The major portion of this activity is presumed to be cyanocobalamin.

2 This work was supported, in part, by grants from Hoffman LaRoche, Inc., The Nutrition Foundation, Inc., The Williams-Waterman Fund of the Research Corporation, and the Division of Research Grants and Fellowships of the National Institutes of Health, United States Public Health Service.

3 A preliminary report of this investigation has appeared in Fed. Proc., 12: 428, 1953.

4 Present address; Division of Biochemistry, Clinical and Pathological Laboratories, The Rochester General Hospital, Rochester, New York.

5 Markle Scholar in Medical Science.

Manuscript received 12 November 1954.





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