Hypoxanthine-guanine phosphoribosyltransferase deficiency and erythrocyte synthesis of pyridine coenzymes

被引:29
作者
Micheli, V
Sestini, S
Rocchigiani, M
Jacomelli, G
Manzoni, F
Peruzzi, L
Gathof, BS
Zammarchi, E
Pompucci, G
机构
[1] Univ Siena, Dipartimento Biol Mol, I-53100 Siena, Italy
[2] Univ Siena, Ist Clin Pediat, I-53100 Siena, Italy
[3] Univ Cologne, Zent Dienstleistungseinrichtung Transfus Med, D-50924 Cologne, Germany
[4] Osped Pediat Mayer, I-50132 Florence, Italy
关键词
purines; human; nicotinamide adenine dinucleotide; HPRT deficiency; Lesch-Nyhan syndrome;
D O I
10.1016/S0024-3205(99)00205-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purine and pyridine metabolism were studied in ten Lesch-Nyhan patients, with virtually no hypoxanthine-guanine phosphoribosyltransferase (HPRT) activity in erythrocytes. Increased NAD erythrocyte concentrations were found in all patients. Raised activities of two enzymes catalysing NAD synthesis from nicotinic acid (nicotinic acid phosphoribosyltransferase : NAPRT, and NAD synthetase: NADs) was found in erythrocyte lysates from all patients. The two enzymes had normal apparent Km for their substrates and increased Vmax. The rate of synthesis of pyridine nucleotides from nicotinic acid by intact erythrocytes in vitro was also increased in most patients. These findings suggest that raised NAD concentrations in HPRT- erythrocytes are due to enhanced syhthesis as a result of increased enzyme activities.
引用
收藏
页码:2479 / 2487
页数:9
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