Urinary excretion of 5-oxoproline (pyroglutamic aciduria) as an index of glycine insufficiency in normal man

AA Jackson, AV Badaloo, T Forrester… - British journal of …, 1987 - cambridge.org
1. The evidence is accumulating to suggest that glycine, the simplest amino acid, is
conditionally essential in man. Benzoic acid, by conjugation with glycine to form hippuric …

Comparison of urinary 5-L-oxoproline (L-pyroglutamate) during normal pregnancy in women in England and Jamaica

AA Jackson, C Persaud, G Werkmeister… - British Journal of …, 1997 - cambridge.org
Urinary 5-L-oxoproline was measured during normal pregnancies in Southampton, England
and Kingston, Jamaica. The CV of 5-L-oxoproline excretion in urine, determined over 7 d in …

The excretion of 5‐oxoproline in urine, as an index of glycine status, during normal pregnancy

C Persaud, J McDermott, B De Benoist… - … Journal of Obstetrics …, 1989 - Wiley Online Library
The urinary excretion of 5‐oxoproline, which may be used as an index of glycine status, was
investigated in 30 normal pregnant women during different stages of pregnancy and in 18 …

Urinary excretion of 5-L-oxoproline (pyroglutamic acid) is increased during recovery from severe childhood malnutrition and responds to supplemental glycine

C Persaud, T Forrester, AA Jackson - The Journal of nutrition, 1996 - Elsevier
We hypothesized that a limitation in the endogenous formation of glycine might constrain
catch-up growth during recovery from severe childhood malnutrition. The urinary excretion of …

Urinary excretion of 5-L-oxoproline (pyroglutamic acid) is increased in normal adults consuming vegetarian or low protein diets

AA Jackson, C Persaud, TS Meakins, R Bundy - The Journal of nutrition, 1996 - Elsevier
A method for measuring 5-L-oxoproline in urine, which involves isolation by short-column
chromatography, acid hydrolysis to glutamic acid and enzymic assay of glutamic acid, was …

Urinary excretion of 5-L-oxoproline (pyroglutamic acid) during early life in term and preterm infants

AA Jackson, C Persaud, M Hall, S Smith… - Archives of Disease in …, 1997 - fn.bmj.com
Urinary 5-L-oxoproline was measured in term and preterm infants from shortly after birth until
6 weeks of postnatal age to determine their ability to synthesise glycine. In term infants the …

On the mechanism of 5-oxoproline overproduction in 5-oxoprolinuria

A Larsson, B Mattsson - Clinica Chimica Acta, 1976 - Elsevier
The primary metabolic defect in 5-oxoprolinuria (pyroglutamic aciduria) is the lack of
glutathione synthetase. The mechanism of the concomitant overproduction of 5-oxoproline …

Glutathione synthetase deficiency, an inborn error of metabolism involving the γ-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria)

VP Wellner, R Sekura, A Meister… - Proceedings of the …, 1974 - National Acad Sciences
Enzyme studies on placenta, cultured skin fibroblasts, and erythrocytes from two sisters with
the inborn error 5-oxoprolinuria (pyroglutamic aciduria) indicate that the metabolic lesion in …

The clinical measurement of urinary total hydroxyproline excretion

A Gasser, A Celada, B Courvoisier, D Depierre… - Clinica Chimica …, 1979 - Elsevier
The effect of dietary control on the day-to-day variation in total hydroxyproline excretion has
been examined in two studies. In the first, a normal volunteer ate a controlled diet containing …

[引用][C] Amino-acid metabolism

CE Dent, JM Walshe - British Medical Bulletin, 1954 - academic.oup.com
It was possible in this way to trace broadly the main features of amino-acid metabolism in the
mammal, as summarized, for instance, in fig. 1 (Dent, 1954). This shows that the main …