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静脉注射还原型谷胱甘肽治疗早期帕金森病

Reduced intravenous glutathione in the treatment of early Parkinson's disease.

作者信息

Sechi G, Deledda M G, Bua G, Satta W M, Deiana G A, Pes G M, Rosati G

机构信息

Department of Neurology, University of Sassari, Italy.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1996 Oct;20(7):1159-70. doi: 10.1016/s0278-5846(96)00103-0.

Abstract
  1. Several studies have demonstrated a deficiency in reduced glutathione (GSH) in the nigra of patients with Parkinson's Disease (PD). In particular, the magnitude of reduction in GSH seems to parallel the severity of the disease. This finding may indicate a means by which the nigra cells could be therapeutically supported. 2. The authors studied the effects of GSH in nine patients with early, untreated PD. GSH was administered intravenous, 600 mg twice daily, for 30 days, in an open label fashion. Then, the drug was discontinued and a follow-up examination carried-out at 1-month interval for 2-4 months. Thereafter, the patients were treated with carbidopa-levodopa. 3. The clinical disability was assessed by using two different rating scale and the Webster Step-Second Test at baseline and at 1-month interval for 4-6 months. All patients improved significantly after GSH therapy, with a 42% decline in disability. Once GSH was stopped the therapeutic effect lasted for 2-4 months. 4. Our data indicate that in untreated PD patients GSH has symptomatic efficacy and possibly retards the progression of the disease.
摘要
  1. 多项研究表明,帕金森病(PD)患者黑质中的还原型谷胱甘肽(GSH)存在缺乏。特别是,GSH的降低程度似乎与疾病的严重程度平行。这一发现可能表明一种可以对黑质细胞进行治疗支持的方法。2. 作者研究了GSH对9例未经治疗的早期PD患者的影响。以开放标签的方式,静脉注射GSH,每日两次,每次600mg,持续30天。然后,停药,并每隔1个月进行一次随访检查,持续2 - 4个月。此后,患者接受卡比多巴-左旋多巴治疗。3. 在基线以及之后4 - 6个月内每隔1个月,使用两种不同的评分量表和韦伯斯特第二步测试对临床残疾情况进行评估。所有患者在接受GSH治疗后均有显著改善,残疾程度下降了42%。一旦停止使用GSH,治疗效果持续2 - 4个月。4. 我们的数据表明,在未经治疗的PD患者中,GSH具有对症疗效,并且可能延缓疾病进展。

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