Pharmacology & Therapeutics, National University of Ireland, Galway, Ireland.
Pharmacology & Therapeutics, National University of Ireland, Galway, Ireland.
Neuroscience. 2017 Dec 26;367:34-46. doi: 10.1016/j.neuroscience.2017.10.018. Epub 2017 Oct 24.
Parkinson's disease is a common, debilitating, neurodegenerative disorder for which the current gold standard treatment, levodopa (L-DOPA) is symptomatic. There is an urgent, unmet need for neuroprotective or, ideally, neuro-restorative drugs. We describe a 6-hydroxydopamine (6-OHDA) zebrafish model to screen drugs for neuroprotective and neuro-restorative capacity. Zebrafish larvae at two days post fertilization were exposed to 6-OHDA for three days, with co-administration of test drugs for neuroprotection experiments, or for 32 h, with subsequent treatment with test drugs for neuro-restoration experiments. Locomotor activity was assessed by automated tracking and dopaminergic neurons were visualized by tyrosine hydroxylase immuno-histochemistry. Exposure to 6-OHDA for either 32 h or 3 days induced similar, significant locomotor deficits and neuronal loss in 5-day-old larvae. L-DOPA (1 mM) partially restored locomotor activity, but was neither neuroprotective nor neuro-restorative, mirroring the clinical situation. The calcium channel blocker, isradipine (1 µM) did not prevent or reverse 6-OHDA-induced locomotor deficit or neuronal loss. However, both the tetracycline analog, minocycline (10 µM), and the monoamine oxidase B inhibitor, rasagiline (1 µM), prevented the locomotor deficits and neuronal loss due to three-day 6-OHDA exposure. Importantly, they also reversed the locomotor deficit caused by prior exposure to 6-OHDA; rasagiline also reversed neuronal loss and minocycline partially restored neuronal loss due to prior 6-OHDA, making them candidates for investigation as neuro-restorative treatments for Parkinson's disease. Our findings in zebrafish reflect preliminary clinical findings for rasagiline and minocycline. Thus, we have developed a zebrafish model suitable for high-throughput screening of putative neuroprotective and neuro-restorative therapies for the treatment of Parkinson's disease.
帕金森病是一种常见的、使人虚弱的神经退行性疾病,目前的金标准治疗药物左旋多巴(L-DOPA)仅能对症治疗。因此,人们迫切需要具有神经保护或理想的神经修复作用的药物。我们描述了一种 6-羟多巴胺(6-OHDA)斑马鱼模型,用于筛选具有神经保护和神经修复能力的药物。受精后两天的斑马鱼幼虫在暴露于 6-OHDA 3 天后,同时给予测试药物进行神经保护实验,或暴露于 6-OHDA 32 小时后,用测试药物进行神经修复实验。通过自动跟踪评估运动活动,并用酪氨酸羟化酶免疫组织化学观察多巴胺能神经元。暴露于 6-OHDA 32 小时或 3 天都会导致 5 天大的幼虫出现类似的、显著的运动缺陷和神经元丢失。L-DOPA(1mM)部分恢复了运动活动,但既没有神经保护作用,也没有神经修复作用,与临床情况相符。钙通道阻滞剂异搏定(1µM)既不能预防也不能逆转 6-OHDA 引起的运动缺陷或神经元丢失。然而,四环素类似物米诺环素(10µM)和单胺氧化酶 B 抑制剂雷沙吉兰(1µM)都能预防由于 3 天 6-OHDA 暴露引起的运动缺陷和神经元丢失。重要的是,它们还能逆转先前暴露于 6-OHDA 引起的运动缺陷;雷沙吉兰还能逆转神经元丢失,米诺环素部分恢复了由于先前 6-OHDA 引起的神经元丢失,使它们成为治疗帕金森病的神经修复治疗的候选药物。我们在斑马鱼中的发现反映了雷沙吉兰和米诺环素的初步临床发现。因此,我们开发了一种适合用于筛选治疗帕金森病的潜在神经保护和神经修复疗法的高通量斑马鱼模型。