Pescarmona G P, Bracone A, David O, Sartori M L, Bosia A
Acta Biol Med Ger. 1977;36(5-6):759-63.
NAD is synthesized in red cell from nicotinic acid and PRPP through the formation of nicotinate mononucleotide and desamido-NAD. Synthesis of one mole of NAD requires two moles of ATP. NADP comes from NAD phosphorylation by NAD-kinase (EC.2.7.1.23). NAD and NADP analysis on a population with ATP level ranging from 800 to 2500 nmoles/ml red cells showed a close correlation between ATP and pyridine cofactors. Moreover, NADP level appeared to be dependent of the redox-state of NADP/NADPH couple. Subjects with low NADPH (G-6-PD) deficient red cells, Hb Köln) showed lower NADtot/NADPtot ratio, suggesting a NAD-kinase equilibrium shift toward NADP related to lower levels of the negative effector NADPH, as already described in rat liver.
烟酰胺腺嘌呤二核苷酸(NAD)在红细胞中由烟酸和5-磷酸核糖焦磷酸(PRPP)通过形成烟酸单核苷酸和脱酰胺-NAD合成。合成一摩尔NAD需要两摩尔ATP。烟酰胺腺嘌呤二核苷酸磷酸(NADP)来自于由NAD激酶(EC.2.7.1.23)催化的NAD磷酸化。对红细胞中ATP水平在800至2500纳摩尔/毫升范围内的人群进行的NAD和NADP分析表明,ATP与吡啶辅因子之间存在密切相关性。此外,NADP水平似乎取决于NADP/NADPH偶联的氧化还原状态。红细胞中烟酰胺腺嘌呤二核苷酸磷酸还原型(NADPH)水平较低(葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏、血红蛋白科隆(Hb Köln))的受试者显示出较低的总NAD/总NADP比率,这表明NAD激酶平衡向NADP方向转变,这与负效应物NADPH水平较低有关,正如在大鼠肝脏中已经描述的那样。