†CSIR-Indian Institute of Toxicology Research (CSIR-IITR), 80 MG Marg, Lucknow 226001, India.
§Academy of Scientific and Innovative Research (AcSIR), Delhi 110001, India.
ACS Nano. 2015 May 26;9(5):4850-71. doi: 10.1021/nn506408v. Epub 2015 Apr 22.
Sustained and safe delivery of dopamine across the blood brain barrier (BBB) is a major hurdle for successful therapy in Parkinson's disease (PD), a neurodegenerative disorder. Therefore, in the present study we designed neurotransmitter dopamine-loaded PLGA nanoparticles (DA NPs) to deliver dopamine to the brain. These nanoparticles slowly and constantly released dopamine, showed reduced clearance of dopamine in plasma, reduced quinone adduct formation, and decreased dopamine autoxidation. DA NPs were internalized in dopaminergic SH-SY5Y cells and dopaminergic neurons in the substantia nigra and striatum, regions affected in PD. Treatment with DA NPs did not cause reduction in cell viability and morphological deterioration in SH-SY5Y, as compared to bulk dopamine-treated cells, which showed reduced viability. Herein, we report that these NPs were able to cross the BBB and capillary endothelium in the striatum and substantia nigra in a 6-hydroxydopamine (6-OHDA)-induced rat model of PD. Systemic intravenous administration of DA NPs caused significantly increased levels of dopamine and its metabolites and reduced dopamine-D2 receptor supersensitivity in the striatum of parkinsonian rats. Further, DA NPs significantly recovered neurobehavioral abnormalities in 6-OHDA-induced parkinsonian rats. Dopamine delivered through NPs did not cause additional generation of ROS, dopaminergic neuron degeneration, and ultrastructural changes in the striatum and substantia nigra as compared to 6-OHDA-lesioned rats. Interestingly, dopamine delivery through nanoformulation neither caused alterations in the heart rate and blood pressure nor showed any abrupt pathological change in the brain and other peripheral organs. These results suggest that NPs delivered dopamine into the brain, reduced dopamine autoxidation-mediated toxicity, and ultimately reversed neurochemical and neurobehavioral deficits in parkinsonian rats.
跨血脑屏障(BBB)持续且安全地递多巴胺是治疗帕金森病(PD)这一神经退行性疾病的主要障碍。因此,在本研究中,我们设计了神经递质多巴胺负载的 PLGA 纳米颗粒(DA NPs)以将多巴胺递送至大脑。这些纳米颗粒缓慢且持续地释放多巴胺,表现出减少了在血浆中的多巴胺清除,减少了醌加合物的形成,并且降低了多巴胺的自动氧化。DA NPs 被内化到多巴胺能 SH-SY5Y 细胞以及黑质和纹状体中的多巴胺能神经元中,这些区域在 PD 中受到影响。与接受大量多巴胺处理的细胞相比,DA NPs 处理的 SH-SY5Y 细胞没有导致细胞活力降低和形态恶化,而大量多巴胺处理的细胞显示出活力降低。在此,我们报告称,与接受大量多巴胺处理的细胞相比,这些 NPs 能够穿过血脑屏障和纹状体及黑质中的毛细血管内皮,而大量多巴胺处理的细胞显示出活力降低。在 6-羟多巴胺(6-OHDA)诱导的 PD 大鼠模型中,静脉内全身给予 DA NPs 导致纹状体中的多巴胺及其代谢物水平显著增加,并降低了帕金森病大鼠纹状体中的多巴胺-D2 受体超敏性。此外,DA NPs 显著恢复了 6-OHDA 诱导的帕金森病大鼠的神经行为异常。与 6-OHDA 损伤的大鼠相比,通过 NPs 递多巴胺不会导致 ROS 的额外产生、多巴胺能神经元变性以及纹状体和黑质中的超微结构改变。有趣的是,与 6-OHDA 损伤的大鼠相比,通过纳米制剂递多巴胺既不会引起心率和血压的改变,也不会导致大脑和其他外周器官出现任何突然的病理性变化。这些结果表明, NPs 将多巴胺递送至大脑,减少了多巴胺自动氧化介导的毒性,最终逆转了帕金森病大鼠的神经化学和神经行为缺陷。