Somayajulu-Niţu Mallika, Sandhu Jagdeep K, Cohen Jerome, Sikorska Marianna, Sridhar T S, Matei Anca, Borowy-Borowski Henryk, Pandey Siyaram
Chemistry & Biochemistry, University of Windsor, Windsor, ON, Canada.
BMC Neurosci. 2009 Jul 27;10:88. doi: 10.1186/1471-2202-10-88.
Parkinson's disease, for which currently there is no cure, develops as a result of progressive loss of dopamine neurons in the brain; thus, identification of any potential therapeutic intervention for disease management is of a great importance.
Here we report that prophylactic application of water-soluble formulation of coenzyme Q10 could effectively offset the effects of environmental neurotoxin paraquat, believed to be a contributing factor in the development of familial PD. In this study we utilized a model of paraquat-induced dopaminergic neurodegeneration in adult rats that received three weekly intra-peritoneal injections of the herbicide paraquat. Histological and biochemical analyses of rat brains revealed increased levels of oxidative stress markers and a loss of approximately 65% of dopamine neurons in the substantia nigra region. The paraquat-exposed rats also displayed impaired balancing skills on a slowly rotating drum (rotorod) evidenced by their reduced spontaneity in gait performance. In contrast, paraquat exposed rats receiving a water-soluble formulation of coenzyme Q10 in their drinking water prior to and during the paraquat treatment neither developed neurodegeneration nor reduced rotorod performance and were indistinguishable from the control paraquat-untreated rats.
Our data confirmed that paraquat-induced neurotoxicity represents a convenient rat model of parkinsonian neurodegeneration suitable for mechanistic and neuroprotective studies. This is the first preclinical evaluation of a water-soluble coenzyme Q10 formulation showing the evidence of prophylactic neuroprotection at clinically relevant doses.
帕金森病目前无法治愈,其发病是由于大脑中多巴胺神经元的逐渐丧失;因此,确定任何潜在的疾病管理治疗干预措施都非常重要。
我们在此报告,预防性应用辅酶Q10的水溶性制剂可有效抵消环境神经毒素百草枯的影响,百草枯被认为是家族性帕金森病发展的一个促成因素。在本研究中,我们利用成年大鼠百草枯诱导的多巴胺能神经退行性变模型,这些大鼠每周接受三次腹腔注射除草剂百草枯。对大鼠大脑的组织学和生化分析显示氧化应激标志物水平升高,黑质区域约65%的多巴胺神经元丧失。接触百草枯的大鼠在缓慢旋转的鼓(转棒)上的平衡技能也受损,表现为步态表现的自发性降低。相比之下,在百草枯治疗之前和期间,饮用含辅酶Q10水溶性制剂的百草枯暴露大鼠既未发生神经退行性变,转棒性能也未降低,与未接受百草枯治疗的对照大鼠没有区别。
我们的数据证实,百草枯诱导的神经毒性代表了一种适用于机制和神经保护研究的方便的帕金森病神经退行性变大鼠模型。这是对水溶性辅酶Q10制剂的首次临床前评估,显示了在临床相关剂量下预防性神经保护的证据。