Lücke Thomas, Tsikas Dimitrios, Kanzelmeyer Nele, Vaske Bernhard, Das Anibh Martin
Department of Pediatrics, Medical School of Hannover, Carl Neuberg Str. 1, D-30625 Hannover, Germany.
Metabolism. 2006 Dec;55(12):1599-603. doi: 10.1016/j.metabol.2006.07.020.
Citrullinemia is an inborn error of the urea cycle with deficiency of the argininosuccinate synthase. It is characterized by elevated concentrations of l-citrulline and decreased levels of l-arginine in body fluids. Asymmetric dimethylarginine is an endogenous inhibitor of nitric oxide synthase that converts l-arginine to l-citrulline and nitric oxide (NO). Asymmetric dimethylarginine is hydrolyzed by the enzyme dimethylarginine dimethylaminohydrolase to l-citrulline and dimethylamine. Elevation of l-citrulline in citrullinemia prompted us to study the l-arginine/NO pathway in this disorder. In 8 children with citrullinemia (3 days to 3 years of age), elevated plasma levels of asymmetric dimethylarginine (P = .028) were found compared with age-matched healthy children. We hypothesize that the l-arginine/NO pathway plays a role in the pathophysiology of citrullinemia.
瓜氨酸血症是一种尿素循环的先天性代谢缺陷,由精氨琥珀酸合成酶缺乏所致。其特征是体液中L-瓜氨酸浓度升高,L-精氨酸水平降低。不对称二甲基精氨酸是一氧化氮合酶的内源性抑制剂,该酶可将L-精氨酸转化为L-瓜氨酸和一氧化氮(NO)。不对称二甲基精氨酸被二甲基精氨酸二甲胺水解酶水解为L-瓜氨酸和二甲胺。瓜氨酸血症中L-瓜氨酸的升高促使我们研究该疾病中的L-精氨酸/NO途径。在8名年龄为3天至3岁的瓜氨酸血症患儿中,与年龄匹配的健康儿童相比,发现其血浆中不对称二甲基精氨酸水平升高(P = 0.028)。我们推测L-精氨酸/NO途径在瓜氨酸血症的病理生理学中起作用。