Decoulx M, Wemeau J L, Racadot-Leroy N, Grimbert I, Proye C, Plane C
Service de clinique médicale, CHR, Lille.
Rev Med Interne. 1987 Sep-Oct;8(4):383-8. doi: 10.1016/s0248-8663(87)80010-3.
Alpha-methyl-paratyrosine (Demser) is a specific inhibitor of tyrosine hydroxylation to dopa. It is administered orally and may be given in combination with symptomatic treatments to reduce the hypersecretion of catecholamines. We report two cases of malignant phaeochromocytoma in which this drug was used. A pharmacological study of the compound is presented, and the literature on its long-term use in the treatment of malignant phaeochromocytoma is reviewed. In our second patient, who received alpha-methyl-paratyrosine for 9 months, a study of changes in differential catecholamine excretion showed that the urinary catecholamines were redistributed, with an increase in the dopamine/norepinephrine ratio. An HPLC study of urinary excretion of catecholamines demonstrated that their levels cannot be significantly increased by excretion of alpha-methyl-paratyrosine or its metabolites.
α-甲基对酪氨酸(德美罗)是一种将酪氨酸羟化为多巴的特异性抑制剂。它通过口服给药,可与对症治疗联合使用,以减少儿茶酚胺的过度分泌。我们报告了两例使用该药物的恶性嗜铬细胞瘤病例。文中对该化合物进行了药理学研究,并回顾了其长期用于治疗恶性嗜铬细胞瘤的相关文献。在我们的第二位患者中,其接受α-甲基对酪氨酸治疗9个月,对儿茶酚胺排泄差异变化的研究表明,尿儿茶酚胺重新分布,多巴胺/去甲肾上腺素比值增加。一项对儿茶酚胺尿排泄的高效液相色谱研究表明,α-甲基对酪氨酸或其代谢产物的排泄不会使儿茶酚胺水平显著升高。