GM1 Ganglioside as a Disease-Modifying Therapeutic for Parkinson's Disease: A Multi-Functional Glycosphingolipid That Targets Multiple Parkinson's Disease-Relevant Pathogenic Mechanisms

被引:3
|
作者
Schneider, Jay S. S. [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol & Genom Med, Philadelphia, PA 19107 USA
关键词
GM1; ganglioside; Parkinson's disease; disease modification; ALPHA-SYNUCLEIN; DOPAMINERGIC-NEURONS; MONOSIALOGANGLIOSIDE GM1; OXIDATIVE STRESS; SUBSTANTIA-NIGRA; HUMAN-BRAIN; NEUROTOXICITY; PATHOLOGY; ROLES; MODEL;
D O I
10.3390/ijms24119183
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parkinson's disease (PD) is a progressive neurodegenerative disorder affecting millions of patients worldwide. Many therapeutics are available for treating PD symptoms but there is no disease-modifying therapeutic that has been unequivocally shown to slow or stop the progression of the disease. There are several factors contributing to the failure of many putative disease-modifying agents in clinical trials and these include the choice of patients and clinical trial designs for disease modification trials. Perhaps more important, however, is the choice of therapeutic, which for the most part, has not taken into account the multiple and complex pathogenic mechanisms and processes involved in PD. This paper discusses some of the factors contributing to the lack of success in PD disease-modification trials, which have mostly investigated therapeutics with a singular mechanism of action directed at one of the many PD pathogenic processes, and suggests that an alternative strategy for success may be to employ multi-functional therapeutics that target multiple PD-relevant pathogenic mechanisms. Evidence is presented that the multi-functional glycosphingolipid GM1 ganglioside may be just such a therapeutic.
引用
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页数:12
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