Schneider J S
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University Philadelphia, Pennsylvania 19107, USA.
Ann N Y Acad Sci. 1998 Jun 19;845:363-73. doi: 10.1111/j.1749-6632.1998.tb09688.x.
Since the early 1980s, numerous studies have been reported by laboratories around the world documenting the beneficial effects of GM1 ganglioside treatment on the damaged dopamine system in various animal and in vitro models. Based on the strength of these data, the first clinical studies designed to assess the efficacy and safety of chronic GM1 use in the treatment of Parkinson's disease were performed. In a double-blind placebo-controlled study, significant improvements in GM1-treated patients were demonstrated in clinical motor ratings, timed tests of motor function, activities of daily living, and some aspects of neuropsychological functioning. Patients who have elected to continue using GM1 in an open extension trial have either continued to improve over time or have shown initial functional improvements and their disease has remained stable (i.e., no symptom progression) after two years. These results suggest that long-term use of GM1 is safe and may work to partially reverse the degenerative process in established Parkinson's disease patients.
自20世纪80年代初以来,世界各地的实验室报告了大量研究,记录了在各种动物和体外模型中,神经节苷脂GM1治疗对受损多巴胺系统的有益作用。基于这些数据的力度,开展了首批旨在评估长期使用GM1治疗帕金森病的疗效和安全性的临床研究。在一项双盲安慰剂对照研究中,接受GM1治疗的患者在临床运动评分、运动功能定时测试、日常生活活动以及神经心理功能的某些方面均有显著改善。在一项开放扩展试验中选择继续使用GM1的患者,要么随着时间的推移持续改善,要么在两年后显示出初始功能改善且病情保持稳定(即症状无进展)。这些结果表明,长期使用GM1是安全的,并且可能有助于部分逆转已确诊帕金森病患者的退行性病变过程。