Davison A S, Norman B, Milan A M, Hughes A T, Khedr M, Rovensky J, Gallagher J A, Ranganath L R
Department of Clinical Biochemistry and Metabolic Medicine, Liverpool Clinical Laboratories, Royal Liverpool University Hospitals Trust, Liverpool, UK.
Bone and Joint Research Group, Musculoskeletal Biology, University of Liverpool, Liverpool, UK.
JIMD Rep. 2018;41:1-10. doi: 10.1007/8904_2017_72. Epub 2017 Nov 17.
One of the major metabolic consequences of using nitisinone to treat patients with alkaptonuria is that circulating tyrosine concentrations increase. As tyrosine is required for the biosynthesis of catecholamine neurotransmitters, it is possible that their metabolism is altered as a consequence. Herein we report the 24-h urinary excretion of normetadrenaline (NMA), metadrenaline (MA), 3-methoxytyramine (3-MT) (catecholamine metabolites) and 5-hydroxyindole acetic acid (5-HIAA, metabolite of serotonin) in a cohort of AKU patients before and after a 4-week treatment trial with nitisinone.
24 h urinary excretions of NMA, MA, 3-MT and 5-HIAA were determined by liquid chromatography tandem mass spectrometry. Interassay coefficient of variation was <10% for all analytes measured, at all concentrations tested.
Urine samples were assayed at baseline (pre-nitisinone, n = 36) and 4 weeks later; 7 received no nitisinone (4 male, mean age (±SD) 46.3 (16.4) years), and 29 received a daily dose of nitisinone [1 mg (n = 7, 6 male, mean age 45.9 (10.9) years), 2 mg (n = 8, 5 male, mean age 43.9 (13.7) years), 4 mg (n = 8, 5 male, mean age 47.3 (10.7) years) and 8 mg (n = 6, 4 male, mean age 53.8 (8.3) years)]. 3-MT concentrations increase significantly (p < 0.01, at all doses) following nitisinone therapy but not in a dose-dependent manner. NMA concentrations decreased (p < 0.05, at all doses) following nitisinone therapy at all doses. 5-HIAA concentrations decreased following nitisinone therapy and were significantly lower at a daily dose of 8 mg only (p < 0.05).
This study shows that catecholamine and serotonin metabolism is altered by treatment with nitisinone.
使用尼替西农治疗尿黑酸尿症患者的主要代谢后果之一是循环酪氨酸浓度升高。由于儿茶酚胺神经递质的生物合成需要酪氨酸,因此其代谢可能会因此而改变。在此,我们报告了一组尿黑酸尿症患者在接受为期4周的尼替西农治疗试验前后,去甲肾上腺素(NMA)、变肾上腺素(MA)、3-甲氧基酪胺(3-MT)(儿茶酚胺代谢物)和5-羟吲哚乙酸(5-HIAA,血清素代谢物)的24小时尿排泄情况。
采用液相色谱串联质谱法测定NMA、MA、3-MT和5-HIAA的24小时尿排泄量。在所有测试浓度下,所有被测分析物的批内变异系数均<10%。
在基线(尼替西农治疗前,n = 36)和4周后对尿样进行检测;7例未接受尼替西农治疗(4例男性,平均年龄(±标准差)46.3(16.4)岁),29例接受每日剂量的尼替西农治疗[1 mg(n = 7,6例男性,平均年龄45.9(10.9)岁),2 mg(n = 8,5例男性,平均年龄43.9(13.7)岁),4 mg(n = 8,5例男性,平均年龄47.3(10.7)岁)和8 mg(n = 6,4例男性,平均年龄53.8(8.3)岁)]。尼替西农治疗后3-MT浓度显著升高(所有剂量下p < 0.01),但不是剂量依赖性的。所有剂量的尼替西农治疗后NMA浓度均降低(所有剂量下p < 0.05)。尼替西农治疗后5-HIAA浓度降低,仅在每日剂量8 mg时显著降低(p < 0.05)。
本研究表明,尼替西农治疗会改变儿茶酚胺和血清素的代谢。