Akkhawattanangkul Y, Maiti P, Xue Y, Aryal D, Wetsel W C, Hamilton D, Fowler S C, McDonald M P
Department of Comparative Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Neurology, University of Tennessee Health Science Center, Memphis, TN, USA.
Genes Brain Behav. 2017 Jun;16(5):522-536. doi: 10.1111/gbb.12377. Epub 2017 Apr 18.
Parkinson's disease is a debilitating neurodegenerative condition for which there is no cure. Converging evidence implicates gangliosides in the pathogenesis of several neurodegenerative diseases, suggesting a potential new class of therapeutic targets. We have shown that interventions that simultaneously increase the neuroprotective GM1 ganglioside and decrease the pro-apoptotic GD3 ganglioside - such as inhibition of GD3 synthase (GD3S) or administration of sialidase - are neuroprotective in vitro and in a number of preclinical models. In this study, we investigated the effects of GD3S deletion on parkinsonism induced by 1-methyl-4phenyl-1,2,3,6-tetrahydropyridine (MPTP). MPTP was administered to GD3S-/- mice or controls using a subchronic regimen consisting of three series of low-dose injections (11 mg/kg/day × 5 days each, 3 weeks apart), and motor function was assessed after each. The typical battery of tests used to assess parkinsonism failed to detect deficits in MPTP-treated mice. More sensitive measures - such as the force-plate actimeter and treadmill gait parameters - detected subtle effects of MPTP, some of which were absent in mice lacking GD3S. In wild-type mice, MPTP destroyed 53% of the tyrosine-hydroxylase (TH)-positive neurons in the substantia nigra pars compacta (SNc) and reduced striatal dopamine 60.7%. In contrast, lesion size was only 22.5% in GD3S-/- mice and striatal dopamine was reduced by 37.2%. Stereological counts of Nissl-positive SNc neurons that did not express TH suggest that neuroprotection was complete but TH expression was suppressed in some cells. These results show that inhibition of GD3S has neuroprotective properties in the MPTP model and may warrant further investigation as a therapeutic target.
帕金森病是一种使人衰弱的神经退行性疾病,目前尚无治愈方法。越来越多的证据表明神经节苷脂参与了多种神经退行性疾病的发病机制,这提示了一类潜在的新治疗靶点。我们已经表明,同时增加神经保护性GM1神经节苷脂并减少促凋亡GD3神经节苷脂的干预措施——如抑制GD3合酶(GD3S)或施用唾液酸酶——在体外和一些临床前模型中具有神经保护作用。在本研究中,我们研究了GD3S缺失对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森综合征的影响。使用由三个低剂量注射系列组成的亚慢性方案(每次11mg/kg/天×5天,间隔3周)将MPTP给予GD3S基因敲除小鼠或对照小鼠,每次注射后评估运动功能。用于评估帕金森综合征的典型测试组未能检测到MPTP处理小鼠的缺陷。更敏感的测量方法——如测力板活动计和跑步机步态参数——检测到了MPTP的细微影响,其中一些在缺乏GD3S的小鼠中不存在。在野生型小鼠中,MPTP破坏了黑质致密部(SNc)中53%的酪氨酸羟化酶(TH)阳性神经元,并使纹状体多巴胺减少60.7%。相比之下,GD3S基因敲除小鼠的损伤大小仅为22.5%,纹状体多巴胺减少了37.2%。对不表达TH的Nissl阳性SNc神经元进行的体视学计数表明,神经保护作用是完全的,但某些细胞中的TH表达受到了抑制。这些结果表明,抑制GD3S在MPTP模型中具有神经保护特性,作为治疗靶点可能值得进一步研究。