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亚甲蓝辅助治疗精神分裂症。

Methylene blue adjuvant therapy of schizophrenia.

作者信息

Deutsch S I, Rosse R B, Schwartz B L, Fay-McCarthy M, Rosenberg P B, Fearing K

机构信息

Department of Veterans Affairs, Medical Center, Department of Psychiatry, Georgetown University School of Medicine, Washington, DC 20422, USA.

出版信息

Clin Neuropharmacol. 1997 Aug;20(4):357-63. doi: 10.1097/00002826-199708000-00008.

DOI:10.1097/00002826-199708000-00008
PMID:9260734
Abstract

There is growing interest in the role of the nitric oxide (NO) pathway in idiopathic psychotic disorders such as schizophrenia. In this preliminary study, we examined the therapeutic efficacy of methylene blue (MB), a "downstream" inhibitor of one of NO's actions, administered orally as an adjuvant to conventional neuroleptic medications. Specifically, MB blocks NO's activation of soluble guanylyl cyclase. MB has previously been reported to have therapeutic effects in the treatment of psychosis and mania. Preclinical data also suggest that MB might possess antipsychotic potential. Participants in the current study were eight patients with schizophrenia who had incomplete responses to conventional antipsychotics (as evidenced by a Brief Psychiatric Rating Scale [BPRS] total score of 35 or more). These patients completed a 4-week open-label study with a 1 week "off", 2 week "on", and one final week "off" design. Measures of treatment efficacy were the BPRS, Schedule for the Assessment of Negative Symptoms, and Clinical Global Improvement Scale administered weekly. Final scores for each outcome measure item were based on the consensus of at least two trained raters present during each rating interview. A statistically significant, albeit modest, decrease in the severity of psychopathology was observed while the subjects were taking MB, and psychopathology significantly worsened when MB was discontinued. The results suggest a need for further study with MB or perhaps other NO-dependent guanylyl cyclase-inhibiting medications.

摘要

一氧化氮(NO)通路在诸如精神分裂症等特发性精神障碍中的作用正受到越来越多的关注。在这项初步研究中,我们考察了亚甲蓝(MB)作为传统抗精神病药物辅助用药口服给药的治疗效果,MB是NO作用之一的“下游”抑制剂。具体而言,MB可阻断NO对可溶性鸟苷酸环化酶的激活作用。此前有报道称MB在治疗精神病和躁狂症方面具有治疗效果。临床前数据也表明MB可能具有抗精神病潜力。本研究的参与者为8例对传统抗精神病药物反应不完全的精神分裂症患者(简明精神病评定量表[BPRS]总分35分及以上可证明)。这些患者完成了一项为期4周的开放标签研究,采用1周“停药”、2周“用药”和最后1周“停药”的设计。治疗效果的评估指标为每周进行的BPRS、阴性症状评定量表和临床总体改善量表。每个结局测量项目的最终得分基于每次评定访谈中至少两名经过培训的评定者的共识。在受试者服用MB期间,观察到精神病理学严重程度有统计学意义的下降,尽管下降幅度不大,而停用MB后精神病理学明显恶化。结果表明需要对MB或其他可能的NO依赖性鸟苷酸环化酶抑制药物进行进一步研究。

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