METABOLISM OF GLUCURONIC ACID IN FATIGUE DUE TO PHYSICAL EXERCISE
Concerning the cause of fatigue, there have been many assumptions on the basis of energy accumulation of substances inducing fatigue. There have been a lot of studies (1, 2) on piling up of the so-called fatigue substances. In the book edited by Katsunuma and Asahina (3), it was reported that the so...
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Published in: | Japanese journal of pharmacology Vol. 16; no. 2; pp. 138 - 156 |
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Abstract | Concerning the cause of fatigue, there have been many assumptions on the basis of energy accumulation of substances inducing fatigue. There have been a lot of studies (1, 2) on piling up of the so-called fatigue substances. In the book edited by Katsunuma and Asahina (3), it was reported that the so-called fatigue substances were found by Ueda, Weichart, Pieron, Knipping, Denisenko, Asahina, Ozawa, Vorobew, Pravdic and Neminsky. They assumed that these substances were the metabolites from degraded protein. As mentioned above, there are many reports concerning the cause of fatigue, but we cannot but conceive some questions for their chemical nature. In our investigation on the appearance of fatigue due to physical exercise, the fact that a certain kind of metabolic substance was produced and accumulated from the energy source consumed by the physical exercise. Our investigation was begun to study the relationship between the change of this metabolic product and the change of glucuronic acid metabolism due to physical exercise in the body. The first experiment was done by Tamura in participation in Abe's studies (4, 5) on agents relieving fatigue and increasing efficiency, in 1942. The summary of this study is as follows: the rat was made to run as long as possible on the rotating belt and the time being almost impossible to run was adopted as running time. The running was repeated three times after a short rest. This running test revealed that the central stimulants such as caffeine and amphetamine prolonged only the 1st running time, while glucose and glucuronic acid prolonged all of the 1st, the 2nd and the 3rd running time. In other words, the reducing agents such as glucose and glucuronic acid much more prevented the appearance of fatigue than the central stimulants. |
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AbstractList | Concerning the cause of fatigue, there have been many assumptions on the basis of energy accumulation of substances inducing fatigue. There have been a lot of studies (1, 2) on piling up of the so-called fatigue substances. In the book edited by Katsunuma and Asahina (3), it was reported that the so-called fatigue substances were found by Ueda, Weichart, Pieron, Knipping, Denisenko, Asahina, Ozawa, Vorobew, Pravdic and Neminsky. They assumed that these substances were the metabolites from degraded protein. As mentioned above, there are many reports concerning the cause of fatigue, but we cannot but conceive some questions for their chemical nature. In our investigation on the appearance of fatigue due to physical exercise, the fact that a certain kind of metabolic substance was produced and accumulated from the energy source consumed by the physical exercise. Our investigation was begun to study the relationship between the change of this metabolic product and the change of glucuronic acid metabolism due to physical exercise in the body. The first experiment was done by Tamura in participation in Abe's studies (4, 5) on agents relieving fatigue and increasing efficiency, in 1942. The summary of this study is as follows: the rat was made to run as long as possible on the rotating belt and the time being almost impossible to run was adopted as running time. The running was repeated three times after a short rest. This running test revealed that the central stimulants such as caffeine and amphetamine prolonged only the 1st running time, while glucose and glucuronic acid prolonged all of the 1st, the 2nd and the 3rd running time. In other words, the reducing agents such as glucose and glucuronic acid much more prevented the appearance of fatigue than the central stimulants. |
Author | ITO, HIROO KITA, SHINICHI TOMIZAWA, SETSUO SUGURO, NOBUO MASUDA, MICHIO TAMURA, SHUNKICHI NAKAI, KAZUHITO TSUTSUMI, SHOJI KIZU, KOJI |
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References | 20) LEVVY, G.A. AND STOREY, I.D.E.: Biochem. J. 44, 295 (1949 6) MASUYAMA, G. AND HosojiMA, C.: Medicine and Biology 1, 570 (1942 5) ABE, K.: Folia pharmacol. japon. 44, 19§ (1944 19) TAMURA, S., TSUTSUMI, S. AND Kizu, K.: Folia pharmacol. japon. 59, 106 (1963 11) TAMURA, S. AND KITA, S.: Ibid. 60, 10§ (1964 18) FUJII, Y.: Biochemical Examination, Ed. 2, p. 216, Nanzan-do, Tokyo (1940 15) TAMURA, S., TSUTSUMI, S. AND Kizu, K.: Ibid. 59, 78 (1963 12) AMMON, R.: Pflug. Arch. ges. Physiol. 233, 486 (1933 21) FUKUHARA, T.: Examination Method of Physiology, p. 139, Nanzan-do, Tokyo (1956 9) TAMURA, S. AND KITTA, T.: Folia pharmacol. japon. 46, 148§ (1949 16) TAMURA, S., TsursuMi, S. AND Kizu, K.: Ibid. 59, 99 (1963 14) TAMURA, S., TSUTSUMI, S. AND Kizu, K.: Folia pharmacol. japon. 59, 70 (1963 1) SIMONOSON, E.: Ergebn. Physiol. 37, 200 (1935 2) ATZER, E.: Ibid. 40, 581 (1938 8) MASUYAMA, G.: Ibid. 2, 245 (1942 4) ABE, K.: Studies on Agents Relieving Fatigue and Increasing Efficiency, unpublished 7) MASUYAMA, G. AND HosoJiMA, C.: Ibid. 2, 17 (1942 10) TAMURA, S., TSUTSUMI, S. AND KIZU, K.: Ibid. 59, 91 (1963 17) FISHMAN, W.H. AND GREEN, S.: Jbiol. Chem. 219, 527 (1955 23) DUTTON, G.J.: Report of the 10th Glucuronic Acid Symposium, unpublished (1964 3) KATSUNUMA, S. AND ASAHINA, K.: Fatigue, Sogen-sha, Tokyo (1948 13) ASANO, M., AKITANI, S. AND UKITA, C.: The Method of Chemical Experiments, p. 329, Nanzan-do, Tokyo (1952 22) AKABORI, S.: Method of Investigation about Enzyme, Ed. 1, IV, p. 763, Asakura-shoten, Tokyo (1961 Fujii (10.1254/jjp.16.138_bib18) 1940 Tamura (10.1254/jjp.16.138_bib10) 1963; 59 Katsunuma (10.1254/jjp.16.138_bib3) 1948 Tamura (10.1254/jjp.16.138_bib11) 1964; 60 Fukuhara (10.1254/jjp.16.138_bib21) 1956 Asano (10.1254/jjp.16.138_bib13) 1952 Masuyama (10.1254/jjp.16.138_bib6) 1942; 1 Fishman (10.1254/jjp.16.138_bib17) 1955; 219 10.1254/jjp.16.138_bib23 Ammon (10.1254/jjp.16.138_bib12) 1933; 233 Akabori (10.1254/jjp.16.138_bib22) 1961 Masuyama (10.1254/jjp.16.138_bib8) 1942; 2 Tamura (10.1254/jjp.16.138_bib9) 1949; 46 Tamura (10.1254/jjp.16.138_bib16) 1963; 59 Simonoson (10.1254/jjp.16.138_bib1) 1935; 37 Atzer (10.1254/jjp.16.138_bib2) 1938; 40 10.1254/jjp.16.138_bib4 Abe (10.1254/jjp.16.138_bib5) 1944; 44 Tamura (10.1254/jjp.16.138_bib15) 1963; 59 Levvy (10.1254/jjp.16.138_bib20) 1949; 44 Masuyama (10.1254/jjp.16.138_bib7) 1942; 2 Tamura (10.1254/jjp.16.138_bib14) 1963; 59 Tamura (10.1254/jjp.16.138_bib19) 1963; 59 |
References_xml | – volume: 59 start-page: 91 year: 1963 ident: 10.1254/jjp.16.138_bib10 publication-title: Ibid. contributor: fullname: Tamura – start-page: 216 year: 1940 ident: 10.1254/jjp.16.138_bib18 contributor: fullname: Fujii – ident: 10.1254/jjp.16.138_bib23 – ident: 10.1254/jjp.16.138_bib4 – volume: 59 start-page: 99 year: 1963 ident: 10.1254/jjp.16.138_bib16 publication-title: Ibid. contributor: fullname: Tamura – start-page: 329 year: 1952 ident: 10.1254/jjp.16.138_bib13 contributor: fullname: Asano – volume: 59 start-page: 70 year: 1963 ident: 10.1254/jjp.16.138_bib14 publication-title: Folia Pharmacol. japon. doi: 10.1254/fpj.59.70 contributor: fullname: Tamura – volume: 37 start-page: 200 year: 1935 ident: 10.1254/jjp.16.138_bib1 publication-title: Ergebn. Physiol. contributor: fullname: Simonoson – volume: 44 start-page: 19§ year: 1944 ident: 10.1254/jjp.16.138_bib5 publication-title: Folia Pharmacol. japon. contributor: fullname: Abe – volume: 59 start-page: 106 year: 1963 ident: 10.1254/jjp.16.138_bib19 publication-title: Folia Pharmacol. japon. doi: 10.1254/fpj.59.106 contributor: fullname: Tamura – volume: 40 start-page: 581 year: 1938 ident: 10.1254/jjp.16.138_bib2 publication-title: Ibid. contributor: fullname: Atzer – volume: 233 start-page: 486 year: 1933 ident: 10.1254/jjp.16.138_bib12 publication-title: Pflüg. Arch. ges. Physiol. doi: 10.1007/BF01751458 contributor: fullname: Ammon – volume: 2 start-page: 17 year: 1942 ident: 10.1254/jjp.16.138_bib7 publication-title: Ibid. contributor: fullname: Masuyama – volume: 44 start-page: 295 year: 1949 ident: 10.1254/jjp.16.138_bib20 publication-title: Biochem. J. doi: 10.1042/bj0440295 contributor: fullname: Levvy – start-page: 139 year: 1956 ident: 10.1254/jjp.16.138_bib21 contributor: fullname: Fukuhara – volume: 60 start-page: 10§ year: 1964 ident: 10.1254/jjp.16.138_bib11 publication-title: Ibid. contributor: fullname: Tamura – volume: 59 start-page: 78 year: 1963 ident: 10.1254/jjp.16.138_bib15 publication-title: Ibid. contributor: fullname: Tamura – year: 1948 ident: 10.1254/jjp.16.138_bib3 contributor: fullname: Katsunuma – start-page: 763 year: 1961 ident: 10.1254/jjp.16.138_bib22 contributor: fullname: Akabori – volume: 2 start-page: 245 year: 1942 ident: 10.1254/jjp.16.138_bib8 publication-title: Ibid. contributor: fullname: Masuyama – volume: 46 start-page: 148§ year: 1949 ident: 10.1254/jjp.16.138_bib9 publication-title: Folia Pharmacol. japon. contributor: fullname: Tamura – volume: 219 start-page: 527 year: 1955 ident: 10.1254/jjp.16.138_bib17 publication-title: J. biol. Chem. doi: 10.1016/S0021-9258(18)65974-5 contributor: fullname: Fishman – volume: 1 start-page: 570 year: 1942 ident: 10.1254/jjp.16.138_bib6 publication-title: Medicine and Biology contributor: fullname: Masuyama |
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SubjectTerms | Animals Anura Chromatography Fatigue - metabolism Glucuronates - metabolism Heart - drug effects Kidney - analysis Liver - analysis Liver Glycogen - analysis Rats |
Title | METABOLISM OF GLUCURONIC ACID IN FATIGUE DUE TO PHYSICAL EXERCISE |
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