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Experimental Biology and Medicine | 1958

Further properties of isoglutamine-oxytocin; inhibition of pressor activity of vasopressin.

Charlotte Ressler; Julian R. Rachele

Summary 1) The isoglutamine isomer of oxytocin has been found to inhibit significantly the pressor activity of administered vasopressin in the anesthetized rat. 2) Various data suggest that acetic acid is lost when the polypeptide acetate is rigorously dried. Isoglutamine-oxytocin forms a crystalline flavianate salt.


Archives of Biochemistry and Biophysics | 1959

Hydrogen isotope effects in the in vivo utilization of formate.

Julian R. Rachele; Edward J. Kuchinskas; Joseph E. Knoll; Maxwell L. Eidinoff

Abstract The hydrogen isotope effects in the utilization of formate in the rat were investigated with formate labeled intermolecularly with deuterium, tritium, and C 14 . Following the administration of this triply labeled formate, the isotope ratios of the formate excreted in the urine and of the methyl groups of tissue choline and creatine were determined and compared with the same ratios in the injected formate. The results indicate extensive selection among the hydrogen isotopes during the metabolism of formate. Intramolecular multiple labeling is suggested as a means of allowing less equivocal interpretations of isotope ratios in studies of the metabolism of C-H units.


Archives of Biochemistry and Biophysics | 1959

The utilization in vivo of deuterio-C14 formate, labeled intramolecularly.

Julian R. Rachele; Hugo Aebi

Abstract The utilization of formate labeled in the same molecule i.e., intramolecularly, with deuterium and C 14 was investigated in the rat. The deuterium and the C 14 contents of the urinary formate and of the methyl groups of choline and creatine, derived from formate, demonstrated the absence of the hydrogen isotope effects noted in earlier experiments performed with precursors labeled in separate molecules with the isotopes of carbon and hydrogen.


Biochimica et Biophysica Acta | 1953

Effect of the presence of labile methyl groups in the diet on labile methyl neogenesis

Vincent du Vigneaud; John M. Kinney; John Eric Wilson; Julian R. Rachele

Abstract The incorporation of deuterium from isotopically labelled body water into the methyl groups of body choline has been used as an indication of methyl synthesis in the rat in vivo. As a test of this concept the amount of isotope appearing in the body choline of rats on a methyl-free diet has been compared with that in rats receiving choline me methionine in the diet. The animals growing well without a source of methyl groups in the diet were found to incorporate approximately four times as much isotope into body choline as animals given choline or methionine.


Archives of Biochemistry and Biophysics | 1959

Hydrogen isotope effects in the oxidation of labeled formate in vivo.

Edward J. Kuchinskas; Antonio Horvath; Julian R. Rachele

Abstract A hydrogen isotope effect has been demonstrated in the in vivo oxidation of formate to CO 2 . It has been suggested that this phenomenon may contribute in great part to the hydrogen isotope effects observed in a previous investigation on the in vivo utilization of formate (1).


Journal of Biological Chemistry | 1947

A synthesis of methionine containing radiocarbon in the methyl group.

Donald B. Melville; Julian R. Rachele; Elizabeth B. Keller


Science | 1950

The Biological Synthesis of "Labile Methyl Groups"

V. Du Vigneaud; Charlotte Ressler; Julian R. Rachele


Journal of the American Chemical Society | 1952

A TEST OF TRITIUM AS A LABELING DEVICE IN A BIOLOGICAL STUDY

Walter G. Verly; Julian R. Rachele; V. du Vigneaud; M.L. Eidinoff; J.E. Knoll


Journal of the American Chemical Society | 1951

One-carbon compounds in the biosynthesis of "biologically labile" methyl group.

V. du Vigneaud; Walter G. Verly; John Eric Wilson; Julian R. Rachele; Charlotte Ressler; John M. Kinney


Journal of Nutrition | 1951

The synthesis of " biologically labile" methyl groups in the germ-free rat.

Vincent du Vigneaud; Charlotte Ressler; Julian R. Rachele; James A. Reyniers; Thomas D. Luckey

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Lester J. Reed

University of Texas at Austin

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