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在帕金森病部分损伤模型中,联合给予载有血管内皮生长因子(VEGF)和胶质细胞源性神经营养因子(GDNF)的纳米球可提高抗帕金森病疗效。

Increased antiparkinson efficacy of the combined administration of VEGF- and GDNF-loaded nanospheres in a partial lesion model of Parkinson's disease.

作者信息

Herrán Enara, Requejo Catalina, Ruiz-Ortega Jose Angel, Aristieta Asier, Igartua Manoli, Bengoetxea Harkaitz, Ugedo Luisa, Pedraz Jose Luis, Lafuente Jose Vicente, Hernández Rosa Maria

机构信息

NanoBioCel Group, Laboratory of Pharmaceutics, University of the Basque Country (UPV/EHU), School of Pharmacy, Vitoria, Spain ; Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Vitoria, Spain.

LaNCE, Department of Neurosciences, University of the Basque Country (UPV/EHU), Leioa, Spain.

出版信息

Int J Nanomedicine. 2014 May 27;9:2677-87. doi: 10.2147/IJN.S61940. eCollection 2014.

Abstract

Current research efforts are focused on the application of growth factors, such as glial cell line-derived neurotrophic factor (GDNF) and vascular endothelial growth factor (VEGF), as neuroregenerative approaches that will prevent the neurodegenerative process in Parkinson's disease. Continuing a previous work published by our research group, and with the aim to overcome different limitations related to growth factor administration, VEGF and GDNF were encapsulated in poly(lactic-co-glycolic acid) nanospheres (NS). This strategy facilitates the combined administration of the VEGF and GDNF into the brain of 6-hydroxydopamine (6-OHDA) partially lesioned rats, resulting in a continuous and simultaneous drug release. The NS particle size was about 200 nm and the simultaneous addition of VEGF NS and GDNF NS resulted in significant protection of the PC-12 cell line against 6-OHDA in vitro. Once the poly(lactic-co-glycolic acid) NS were implanted into the striatum of 6-OHDA partially lesioned rats, the amphetamine rotation behavior test was carried out over 10 weeks, in order to check for in vivo efficacy. The results showed that VEGF NS and GDNF NS significantly decreased the number of amphetamine-induced rotations at the end of the study. In addition, tyrosine hydroxylase immunohistochemical analysis in the striatum and the external substantia nigra confirmed a significant enhancement of neurons in the VEGF NS and GDNF NS treatment group. The synergistic effect of VEGF NS and GDNF NS allows for a reduction of the dose by half, and may be a valuable neurogenerative/neuroreparative approach for treating Parkinson's disease.

摘要

目前的研究工作集中在生长因子的应用上,如胶质细胞源性神经营养因子(GDNF)和血管内皮生长因子(VEGF),作为神经再生方法,以预防帕金森病的神经退行性过程。延续我们研究小组之前发表的一项工作,并且为了克服与生长因子给药相关的不同限制,将VEGF和GDNF封装在聚乳酸-羟基乙酸共聚物纳米球(NS)中。这种策略有助于将VEGF和GDNF联合给药到6-羟基多巴胺(6-OHDA)部分损伤大鼠的大脑中,从而实现持续且同时的药物释放。NS的粒径约为200nm,同时添加VEGF NS和GDNF NS在体外对PC-12细胞系具有显著的抗6-OHDA保护作用。一旦将聚乳酸-羟基乙酸共聚物NS植入6-OHDA部分损伤大鼠的纹状体中,在10周内进行苯丙胺旋转行为测试,以检查体内疗效。结果表明,在研究结束时,VEGF NS和GDNF NS显著减少了苯丙胺诱导的旋转次数。此外,纹状体和黑质外侧的酪氨酸羟化酶免疫组织化学分析证实,VEGF NS和GDNF NS治疗组的神经元有显著增加。VEGF NS和GDNF NS的协同作用使剂量减半,可能是一种治疗帕金森病的有价值的神经生成/神经修复方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96b8/4043720/45b0e45dbb03/ijn-9-2677Fig1.jpg

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