Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-29T21:02:36.591Z Has data issue: false hasContentIssue false

Tyrosyluria in marasmus

Published online by Cambridge University Press:  09 March 2007

P. S. Dhatt
Affiliation:
Departments of Paediatrics and Biochemistry, Medical College and Hospital, Rohtak, India
A. S. Saini
Affiliation:
Departments of Paediatrics and Biochemistry, Medical College and Hospital, Rohtak, India
Indu Gupta
Affiliation:
Departments of Paediatrics and Biochemistry, Medical College and Hospital, Rohtak, India
H. C. Mehta
Affiliation:
Departments of Paediatrics and Biochemistry, Medical College and Hospital, Rohtak, India
Harjit Singh
Affiliation:
Departments of Paediatrics and Biochemistry, Medical College and Hospital, Rohtak, India
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

1. Plasma tyrosine and urinary p-hydroxyphenyl lactic acid (PHPLA) and p-hydroxyphenyl acetic acid (PHPAA) were studied in thirty patients with marasmus and twenty normal controls in the same age group.

2. In the control group conventional tyrosyluria was not observed but 30% of the group excreted high levels of PHPAA. In the group with marasmus, plasma tyrosine and urinary PHPLA and PHPAA values were significantly higher than the control values. However only 13.3% of the patients were considered to have conventional tyrosyluria and 52.3% were found to excrete high levels of PHPAA.

3. Administration of ascorbic acid resulted in a reduction of PHPLA excretion while it had no effect on PHPAA excretion.

4. It was inferred that (a) tyrosyluria in marasmus is due to the reduced activity of the hepatic enzyme 4-hydroxyphenyl pyruvate: oxygen oxidoreductase (hydroxylating, decarboxylating) (PHPPA-oxidase; EC 1. 13. 11. 27) due to the deficiency of ascorbic acid and (b) high excretion of PHPAA is related to age and nutrition of the child and is unaffected by the administration of ascorbic acid.

5. It was further inferred that urinary excretion of PHPLA is a reliable index of tyrosyluria.

Type
Papers of direct relevance to Clinical and Human Nutrition
Copyright
Copyright © The Nutrition Society 1979

References

Aggarwal, S. N., Garg, K. N. & Saini, A. S. (1973). Indian J. med. Res. 61, 132.Google Scholar
Dean, R. F. A. & Whitehead, R. G. (1963). Lancet i, 188.CrossRefGoogle Scholar
Felix, K., Leonardhi, G. & Glasenapp, I. Y. (1951). Z. Physiol. Chem. 267, 141.CrossRefGoogle Scholar
Kirberger, E. (1954). Z. Physiol. Chem. 29, 245.CrossRefGoogle Scholar
Knox, W. E. & Goswarni, M. N. D. (1960). Ann. N.Y. Acad. Sci. 92, 158.Google Scholar
Levine, R. J. & Conn, H. O. (1967). J. clin. Invest. 46, 2012.CrossRefGoogle Scholar
Levine, S. Z., Marples, E. & Gordon, H. H. (1941). J. clin. Invest. 20, 199.CrossRefGoogle Scholar
Mathews, J. & Partington, M. W. (1964). Archs Dis. Childh. 39, 371.CrossRefGoogle Scholar
Menkes, J. H. & Avery, M. E. (1963). Bull. Johns Hupkins Hosp. 113, 301.Google Scholar
Morris, J. E., Harper, E. R. & Goldbloom, A. (1950). J. clin. Invest. 29, 325.CrossRefGoogle Scholar
Saini, A. S. (1963). J. Chromat. 19, 619.CrossRefGoogle Scholar
Saini, A. S. (1967). Indian J. med. Res. 55, 51.Google Scholar
Saini, A. S., Nagpal, R. K. & Mehta, H. C. (1975). Indian Pediat. 12, 635.Google Scholar
Saini, A. S., Singh, P. C., Marya, R. K., Garg, B. B. & Singh, I. D. (1970). Indian J. med. Res. 58, 1724.Google Scholar
Sidney, U. & Cooper, J. R. (1952). J. biol. Chem. 196, 229.Google Scholar
Smith, I. (ed.) (1969). In Chromatographic and Electrophoretic Techniques, 3rd ed., pp. 371, 373. London: Heinemann.Google Scholar
Vaughan, V. C. III (ed.) (1975). In Nelson Textbook of Pediatrics, 10th ed., p. 40. Philadelphia: W. B. Saunders.Google Scholar