Rebouche C J
Department of Pediatrics, University of Iowa College of Medicine, Iowa City 52242.
Am J Clin Nutr. 1991 Dec;54(6 Suppl):1147S-1152S. doi: 10.1093/ajcn/54.6.1147s.
It has been suggested that early features of scurvy (fatigue and weakness) may be attributed to carnitine deficiency. Ascorbate is a cofactor for two alpha-ketoglutarate-requiring dioxygenase reactions (epsilon-N-trimethyllysine hydroxylase and gamma-butyrobetaine hydroxylase) in the pathway of carnitine biosynthesis. Carnitine concentrations are variably low in some tissues of scorbutic guinea pigs. Ascorbic acid deficiency in guinea pigs resulted in decreased activity of hepatic gamma-butyrobetaine hydroxylase and renal but not hepatic epsilon-N-trimethyllsine hydroxylase when exogenous substrates were provided. It remains unclear whether vitamin C deficiency has a significant impact on the overall rate of carnitine synthesis from endogenous substrates. Nevertheless, results of studies of enzyme preparations and perfused liver in vitro and of scorbutic guinea pigs in vivo provide compelling evidence for participation of ascorbic acid in carnitine biosynthesis.
有人提出,坏血病的早期症状(疲劳和虚弱)可能归因于肉碱缺乏。抗坏血酸是肉碱生物合成途径中两个需要α-酮戊二酸的双加氧酶反应(ε-N-三甲基赖氨酸羟化酶和γ-丁酰甜菜碱羟化酶)的辅助因子。在患坏血病的豚鼠的某些组织中,肉碱浓度有不同程度的降低。当提供外源性底物时,豚鼠体内的抗坏血酸缺乏导致肝脏γ-丁酰甜菜碱羟化酶活性降低,但肾脏而非肝脏的ε-N-三甲基赖氨酸羟化酶活性降低。目前尚不清楚维生素C缺乏是否会对由内源性底物合成肉碱的总体速率产生重大影响。然而,体外酶制剂和灌注肝脏以及体内患坏血病豚鼠的研究结果为抗坏血酸参与肉碱生物合成提供了有力证据。