STUDIES IN PROTEIN METABOLISM

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1 STUDIES IN PROTEIN METABOLISM XI. THE METABOLIC RELATION OF CREATINE AND CREATININE STUDIED WITH ISOTOPIC NITROGEN* BY KONRAD BLOCH AND RUDOLF SCHOENHEIMER (From the Department of Biochemistry, College of Physicians and Surgeons, Columbia University, New York) (Received for publication, July 29, 1939) Folin (11, on the basis of his findings of the constancy of creatinine excretion and its apparent lack of relation to the intake of protein or creatine, proposed the theory that creatinine formation is wholly independent of creatine and can be taken as a measure of endogenous tissue metabolism. Experiments by Myers and Fine (2), however, demonstrated the close relationship between the creatinine coefficient and body creatine content for a given species. The findings by Rose and Dimmitt (3) and the extended experiments by Benedict and Osterberg (4) who found creatine administration to be followed by excretion of extra creatinine-though delayed and incompletedefinitely proved the biological dehydration of creatine. The slowness of this reaction was taken to indicate that the conversion is not a direct one but proceeds by way of intermediate compounds. Several investigators have recently discussed the possibility that urinary creatinine has also sources other than creatine (5, 6). The nitrogen isotope N15 offers a tool for the study of this biological conversion. We have prepared isotopic creatine (and creatinine) by treatment of isotopic sarcosine with non-isotopic cyanamide. As the nitrogen of the sarcosine contained 4.5 atom per cent excess isotope, the total nitrogen of the resulting creatine had an isotope content of one-third of that, i.e. 1.5 atom per cent. The N15 concentration was high enough to allow a dilution of the * This work was carried out with the aid of grants from the Rockefeller Foundation and the Josiah Macy, Jr., Foundation. 111

2 112 Protein Metabolism. XI creatine nitrogen with several hundred parts of ordinary nitrogen and still be detectable by the mass spectrometric analysis (7). The biological experiments were carried out with rats. Following the administration of the isotopic compounds, creatine from the tissues was converted into creatinine and isolated in that form. For the isolation of creatinine from the urine, the procedures developed by Folin (8) and by Benedict (9) for the urine of humans or dogs were for unknown reasons unsuccessful when applied to rat urines and had to be modified. Our modification, tested with isotopic compounds, leads to the isolation of preformed creatinine only, uncontaminated with creatine nitrogen. In all experiments with creatine feeding the daily dose was 44 mg. per kilo of body weight per day, an amount which roughly corresponds to the daily excretion of creatinine in the urine. The feeding of isotopic creatine resulted in the immediate excretion of isotopic creatinine, without an increase of the total creatinine output or the appearance of creatine in the urine. The results prove the immediate conversion of creatine into creatinine. On the other hand, the isotope concentration in the urinary creatinine obtained in these experiments was small as compared to that in the dietary creatine, indicating that the nitrogen of urinary creatinine represented not merely that of the dietary creatine but that from other sources. It was found that the bulk was derived from body creatine, which in these experiments contained mainly normal nitrogen. In the experiments recorded in Table I, two groups, each of three rats, kept on a normal creatine-free stock diet, were given creatine for 6 days and were then killed. Samples of creatinine were isolated from the urine collected during t,he experimental period, and found to contain and atom per cent excess W5; the body creatine contained and atom per cent. The results indicate that the administered creatine was mixed with the body creatine while the creatinine, which had an only slightly lower isotope concentration, must have been mainly derived from this mixture. The creatinine analyzed had been formed during the period of creatine administration. That from the pooled urines of the 6 day period must have represented mixtures of creatinine samples with continuously increasing isotope concentrations, starting

3 K. Bloch and R. Schoenheimer 113 with zero at the beginning of the experiment. The values found do not give direct information as to whether creatinine was derived only from body creatine. This can be obtained only by studies with a creatine-free diet.l Under such conditions the isotope concentration of both compounds at a given time should be the same. In a third experiment the body creatine of six rats was marked by the nitrogen isotope by keeping our animals during a preliminary period of 6 days on the diet containing isotopic creatine. After a subsequent 5 day period during which the animals received TABLE Convemion of Creatine to Creatinine Three male rats of 200 gm. each on a stock diet were given 44 mg. of creatine (1.5 atom per cent lv excess) per kilo of body weight per day for 6 days. Muscles Internal organs* Pooled urines of 6 day period I Creatine Creatinine Ammonia Urea I N"content Group1 Group II atwm per cent e5ce * Combined heart, lungs, kidneys, liver, testes, spleen, and brain. atom per cent fzvx the same diet without any creatine, they were killed. Body creatine was isolated from one group of animals, and urinary creatinine from the urine samples of both groups, collected only during the last 48 hours. All samples had identical isotope con- 1 If the dietary creatine in these experiments were completely mixed with body creatine and only the resulting mixture were converted into creatinine, the isotope concentration in the urinary creatinine should, on the assumption that it increases linearly with time, have been slightly more than half of that of the body creatine. The values found were somewhat higher, probably because a small proportion of the dietary creatine was converted before its complete distribution over all the body creatine. A direct conversion of only 2 per cent of the dietary creatine could account for the difference observed.

4 114 Protein Metabolism. XI tent (Table II), definitely proving that on a creative-free diet body creatine was the only precursor of creatinine. Any other source would have given rise to a dilution of the isotopic creatinine nitrogen with normal nitrogen. Dietary creatine when given in small amounts is uniformly distributed over the creatine of muscles and organs. From the animals of Experiment 2 (Group II, Table I), creatine was also isolated from the internal organs (liver, kidney, lungs, etc.). This had almost the same isotope concentration as that of the muscles.2 The results of our three experiments, considered together, furthermore indicate that the replacement of the body creatine by TABLE Creatinine Formation on Creatine-Free Diet Two groups of three male rats of 300 gm. each were first given 44 mg. of isotopic creatine (1.5 atom per cent Nib excess) per kilo of body weight for 6 days, and then kept on a creatine-free diet for 5 days, when Group I was killed. Creatine from muscles... Creatinine from urine of last 48 hrs.. II I Group1 N"content Group11 atom per cent ezce.y* newly synthesized creatine proceeds at a very slow rate. The animals in Experiment 3 (Table II), kept on a creatine-free diet 2 Most of the creatine in muscles is known to be present as phosphocreatine. The almost equal distribution of the isotope over the creatine in organs, muscles, and urinary creatinine suggests a rapid replacement of the creatine in phosphocreatine. Hevesy and Rebbe (10) have determined the rate of this process ( molecular rejuvenation of phosphocreatine) by determining the replacement of its other component, phosphoric acid, by employing radioactive phosphorus. They administered marked phosphate ions to frogs and found that 3 hours after injection the phosphorus in the phosphocreatine had 78 per cent of the isotope concentration in the inorganic phosphates in the serum, indicating a 78 per cent rejuvenation of the phosphocreatine. Our findings on the fast rate of rejuvenation of phosphocreatine are thus in accordance with those of these authors.

5 K. Bloch and R. Schoenheimer 115 for 5 days, still had about the same isotope level in their body creatine as the animals in Experiments 1 and 2 (Table I) which were killed at the end of the period of creatine administratione3 The mechanism of creatinine formation in viva is wholly unknown. While the reaction creatine G creatinine is a reversible process in vitro, it is questionable whether it is reversible also in vivo. It is known that the administration of creatinine results in an immediate elimination of extra creatinine, but a quantitative recovery has never been secured (11). If the loss of ingested creatinine were due to its partial conversion into creatine, the administration of isotopic creatinine should result in the formation of significant quantities of isotopic creatine. This, however, was not the case. Three other rats were given isotopic creatinine for 6 days in addition to the stock diet. The isotope content in the urinary creatinine was half of that in the administered creatinine, indicating that half of the urinary material was derived from the diet. The increase of creatinine in the urine corresponded to a recovery of 75 per cent of the dietary creatinine. The creatine isolated from the muscles had normal nitrogen. If only 2 per cent of this substance had been derived from the administered creatinine, it would have been detected in the analytical procedure. The conversion of creatine into creatinine seems therefore to be biologically irreversible. None of our experiments offered any evidence for degradation of either creatine or creatinine. Samples of ammonia or urea isolated from the urine of our animals had only normal nitrogen, a finding totally different from those observed after isotopic amino acids were fed (12). As the total amount of urea nitrogen in the urine is high compared with the amount of creatine or creatinine administered, a small decomposition might have increased the isotope in the urea so little that it escaped detection. The creatine and creatinine samples given were marked only by the isotope in the sarcosine part of the molecule. A replacement of the nitrogen in the NH&Z=NH I (amidine) group by nor- 3 In an experiment not yet published, we have determined the amount of creatine synthesized per day by rats on a creatine-free diet. It corresponds t.o about 2 per cent of the body creatine; i.e., the same amount as was daily excreted in the form of creatinine.

6 116 Protein Metabolism. XI ma1 nitrogen from other sources such as occurs with arginine (13, 14) could not have become apparent. This reaction will be discussed in a forthcoming publication. EXPERIMENTAL Preparation of Isotopic Creatine and Creatinine-Glycine containing 4.50 atom per cent N1j excess prepared according to Schoenheimer and Ratner (15) was converted into sarcosine (16), and the latter treated with cyanamide and a trace of ordinary (non-isotopic) ammonia (17). The over-all yield of creatine, recrystallized from water, was 58 per cent. It contained 1.50 (calculated 1.50) atom per cent N15 excess. Kjeldahl N found 28.0 per cent; calculated Creatinine was prepared by refluxing isotopic creatine with hydrochloric acid and was isolated as the hydrochloride. It contained 1.50 atom per cent N15 excess. Kjeldahl N found 27.8 per cent; calculated Stability of Nitrogen Atoms in Creatine--~O.OOl mole of creatine and mole of ammonium chloride (2.18 at)om per cent N S excess) in 40 cc. of water were refluxed for 24 hours. The solution was made normal in regard to hydrochloric acid, refluxed for 3 hours, and brought to dryness. The product was isolated as potassium creatinine picrate and recrystallized five times from water. After the removal of picric acid from a sample by extraction of the acidified solution with ether, the nitrogen present contained atom per cent N15 excess. This was due to contamination with a minute amount of isotopic ammonia not removed by the repeated recrystallization. It was removed by treating the compound with ordinary ammonia ( washing out process): 80 mg. of the potassium creatine picrate were once recrystallized from water containing 186 mg. of ordinary (nonisotopic) ammonium chloride, and once from water. The creatinine then contained atom per cent N15 excess. If only 1 per cent of the nitrogen of creatine had exchanged with the nitrogen of ammonia, the isotope content of the product would have been per cent. The decrease of isotope during the washing out process could not have been due to back exchange. If the 2 per cent of isotope had originally entered by exchange during 24 hours, it could not have been removed completely (100 per cent) by exchange during the few minutes when it was in contact with normal ammonia.

7 K. Bloch and R. Schoenheimer 117 Isolation of Creatine and Creatinine-Representative samples of creatine from the muscles and organs were obtained by the procedure described previously (14). For the isolation of creatinine the filtered urine was made acid to Congo red with HCl and treated with Lloyd s reagent. This was collected and washed with dilute HCl and then with 2 per cent barium hydroxide solution. The alkaline washings were neutralized to Congo red with sulfuric acid, freed of barium sulfate, and treated with phosphotungstic acid. The precipitate was centrifuged off and washed with a little ice-cold water. Creatinine phosphotungstate was extracted from t,he precipitate wit.h acetone and the acetone removed. The dry residue was suspended in 10 per cent HCl and phosphotung- TABLE III E xcretion of Creatinine Three male rats of 200 gm. of body weight, on a stock diet were given 50 mg. of creatinine (1.5 atom per cent, N15 excess) per kilo of body weight per day for 6 days. Creatine from muscle Non-protein nitrogen Creatinine fromurine... II.714 Ammonia from urine Urea from urine atom per cent emess stic acid removed by extraction with butanol-ether 1 :l. The aqueous solution was brought to dryness in vacua. The residue was dissolved in water and the amount of creatinine present, was determined calorimetrically in an aliquot. The calculated amounts of picric acid and potassium picrate for precipitation of potassium creatinine picrate were added. After recrystallization from a solution containing 0.12 per cent picric acid, the product was analytically pure. The purity of the samples was always tested (a) by determining the creatinine content colorimetrically, and (b) by determining the nitrogen after quantitative removal of picric acid by continuous extraction with ether. The creatinine content of all samples ranged between 18.3 and 18.8 per cent (calculated 18.6 per cent), and the creatinine nitrogen in the samples was found between 6.8 and 7.0 per cent (calculated 6.9).

8 118 Protein Metabolism. XI Separation of Creatinine from Urinary Creatine-Although in our creatine feeding experiments urinary creatine could not be detected calorimetrically, the possibility of small amounts of isotopic dietary creatine being excreted in the urine as such had to be considered. In order to test whether our isolation procedure involved a conversion of creatine into creatinine, the following experiment was carried out. To a normal sample of rat urine containing 25 mg. of creatinine (determined calorimetrically) 5 mg. of isotopic creatine (Nn = 1.5 atom per cent excess) were added. Creatinine was isolated as described before. It contained atom per cent N15 excess. The value found is within the limits of error of the analytical procedure. Feeding Experiments-Male rats of 200 or 300 gm. each were kept in metabolism cages on the following diet: 68 per cent cornstarch, 15 per cent casein, 6 per cent Wesson oil, 2 per cent cod liver oil, 4 per cent salt mixture (18), 5 per cent yeast. Creatine or creatinine was added in solution to the diet. The animals did not change weight appreciably during the short experimental period. All results are given in Tables I to III. SUMMARY 1. The biological conversion of creatine into creatinine has been studied in adult rats by feeding isotopic creatine or creatinine in addition to the stock diet. The compounds were prepared from isotopic glycine as the starting material. The stability of the nitrogen in creatine was investigated. The nitrogen does not exchange in vitro with the nitrogen of ammonia. 2. Creatine samples were isolated from muscles and creatinine from the urine of rats. In the isolation procedure for the latter any conversion of creatine into creatinine was avoided. This was tested with isotopic material. 3. The administration of small amounts of creatine was followed by an almost equal distribution of dietary creatine nitrogen over creatine of muscle and internal organs as well as over the urinary creatinine. The latter is thus derived mainly from the body creatine. 4. In a second series the body creatine of rats was marked with isotopic nitrogen by feeding isotopic creatine during a preliminary period. In the following period, when creatine was omitted

9 K. Bloch and R. Schoenheimer 119 from the diet, the isotope content of the urinary creatinine was identical with that of the body creatine. This indicated that on a creatine-free diet, body creatine is the only source of urinary creatinine. 5. The administration of isotopic creatinine results in the immediate excretion of most of the isotopic material in the urine. No isotope was found in the body creatine. The results indicate that the reaction creatine c creatinine is biologically irreversible. BIBLIOGRAPHY 1. Folin, O., in Festschrift fur 0. Hammarsten, Upsala, iii, 1 (1906). 2. Myers, V. C., and Fine, M. S., J. Biol. Chem., 14, 9 (1913). 3. Rose, W. C., and Dimmitt, F. W., J. Biol. Chem., 20, 345 (1916). 4. Benedict, S. R., and Osterberg, E., J. Biol. Chem., 66, 229 (1923). 5. Thomas, K., Milhorat, A. T., and Techner, F., 2. physiol. Chem., 214, 121 (1932). 6. Terroine, E. F., Champagne, M., and Mourot, G., Bull. Sot. chim. biol., 16, 203 (1933). 7. Rittenberg, D., Keston, A. S., Rosebury, F., and Schoenheimer, R., J. BioZ. Chem., 12 7, 291 (1939). 8. Folin, O., J. BioZ. Chem., 17, 463 (1914). 9. Benedict, S. R., J. BioZ. Chem., 18, 183 (1914). 10. Hevesy, G., and Rebbe, O., Nature, 141, 1097 (1938). 11. Hunter, A., Creatine and creatinine, Monographs on biochemistry, London and New York, 128 (1928). 12. Schoenheimer, R., Ratner, S., and Rittenberg, D., J. BioZ. Chem., 137, 333 (1939); Science, 89, 272 (1939). 13. Schoenheimer, R., Ratner, S., and Rittenberg, D., J. BioZ. Chem., 130, 703 (1939). 14. Foster, G. L., Schoenheimer, R., and Rittenberg, D., J. BioZ. Chem., 127, 319 (1939). 15. Schoenheimer, R., and Ratner, S., J. BioZ. Chem., 127, 301 (1939). 16. Fischer, E., and Bergmann, M., Ann. Chem., 389, 96 (1913). 17. Rosengarten, F., and Strecher, A., Ann. Chem., 167, 1 (1871). 18. Osborne, T. B., and Mendel, L. B., J. BioZ. Chem., 16, 311 (1913).

10 STUDIES IN PROTEIN METABOLISM: XI. THE METABOLIC RELATION OF CREATINE AND CREATININE STUDIED WITH ISOTOPIC NITROGEN Konrad Bloch and Rudolf Schoenheimer J. Biol. Chem. 1939, 131: Access the most updated version of this article at Alerts: When this article is cited When a correction for this article is posted Click here to choose from all of JBC's alerts This article cites 0 references, 0 of which can be accessed free at tml#ref-list-1

A MICROCOLORIMETRIC DETERMINATION OF CREATINE IN URINE BY THE JAFFE REACTION* HERTHA H. TAUSSKY

A MICROCOLORIMETRIC DETERMINATION OF CREATINE IN URINE BY THE JAFFE REACTION* BY HERTHA H. TAUSSKY WITH THE TECHNICAL ASSISTANCE OF GLORIA KURZMANN (From the Russell Sage Institute of Pathology, Department