Wålinder J, Skott A, Carlsson A, Roos B E
Arch Gen Psychiatry. 1976 Apr;33(4):501-5. doi: 10.1001/archpsyc.1976.01770040061011.
Four patients with chronic schizophrenia of stationary character were studied in order to titrate the lowest dose of thioridazine necessary for symptomatic control when the drug is given in combination with the inhibitor of catecholamine synthesis, metyrosine. The study showed 15% to 50% of the pretrial dose level of thioridazine hydrochloride was effective. In the present trial, the 779704 combination was maintained without any alterations in dosage for six months, and the therapeutic effect persisted unchanged. This treatment period was terminated by a double-blind crossover design, and the activity of metyrosine was corroborated in all cases. Plasma drug concentrations and cerebrospinal fluid amine metabolites were measured. The data indicate that schizophrenic symptoms can be profoundly influenced by changes in catecholamine synthesis. Catecholamine-carrying neurons thus seem to be fundamentally involved in those brain functions that are disturbed in schizophrenia. The clinical usefulness of metyrosine in combination with neuroleptic agents deserves more extensive investigation.
为了确定当硫利达嗪与儿茶酚胺合成抑制剂甲酪氨酸联合使用时,控制症状所需的最低剂量,对4例病情稳定的慢性精神分裂症患者进行了研究。研究表明,盐酸硫利达嗪的剂量为治疗前剂量水平的15%至50%时有效。在本次试验中,779704组合维持六个月,剂量未作任何改变,治疗效果持续不变。该治疗期通过双盲交叉设计结束,且在所有病例中均证实了甲酪氨酸的活性。测量了血浆药物浓度和脑脊液胺代谢产物。数据表明,儿茶酚胺合成的变化可对精神分裂症症状产生深远影响。因此,携带儿茶酚胺的神经元似乎从根本上参与了精神分裂症中受到干扰的大脑功能。甲酪氨酸与抗精神病药物联合使用的临床实用性值得更广泛的研究。