a Laboratório de Neurofisiologia, Departamento de Fisiologia , Universidade Federal do Paraná , 81531-990 Curitiba , PR , Brazil.
b Departamento de Morfologia, Fisiologia e Patologia, Escola de Odontologia de Ribeirão Preto (FORP) , Universidade de São Paulo , Av. Café s/n, 14040-904 Ribeirão Preto , SP , Brazil.
Nutr Neurosci. 2018 Jun;21(5):341-351. doi: 10.1080/1028415X.2017.1290928. Epub 2017 Feb 21.
Parkinson's disease (PD) is characterized by deterioration of the nigrostriatal system and associated with chronic neuroinflammation. Glial activation has been associated with regulating the survival of dopaminergic neurons and is thought to contribute to PD through the release of proinflammatory and neurotoxic factors, such as reactive nitric oxide (NO) that triggers or exacerbates neurodegeneration in PD. Polyunsaturated fatty acids (PUFAs) exert protective effects, including antiinflammatory, antiapoptotic, and antioxidant activity, and may be promising for delaying or preventing PD by attenuating neuroinflammation and preserving dopaminergic neurons. The present study investigated the effects of fish oil supplementation that was rich in PUFAs on dopaminergic neuron loss, the density of inducible nitric oxide synthase (iNOS)-immunoreactive cells, and microglia and astrocyte reactivity in the substantia nigra pars compacta (SNpc) and striatal dopaminergic fibers.
The animals were supplemented with fish oil for 50 days and subjected to unilateral intrastriatal 6-hydroxydopamine (6-OHDA)-induced lesions as a model of PD.
Fish oil mitigated the loss of SNpc neurons and nerve terminals in the striatum that was caused by 6-OHDA. This protective effect was associated with reductions of the density of iNOS-immunoreactive cells and microglia and astrocyte reactivity.
These results suggest that the antioxidant and antiinflammatory properties of fish oil supplementation are closely related to a decrease in dopaminergic damage that is caused by the 6-OHDA model of PD.
帕金森病(PD)的特征是黑质纹状体系统恶化,并伴有慢性神经炎症。神经胶质细胞的激活与调节多巴胺能神经元的存活有关,并且被认为通过释放促炎和神经毒性因子(如反应性一氧化氮(NO))来促进 PD,从而引发或加剧 PD 中的神经退行性变。多不饱和脂肪酸(PUFAs)具有保护作用,包括抗炎、抗细胞凋亡和抗氧化活性,并且通过减轻神经炎症和保护多巴胺能神经元,可能有希望延迟或预防 PD。本研究调查了富含 PUFAs 的鱼油补充对多巴胺能神经元丢失、诱导型一氧化氮合酶(iNOS)-免疫反应细胞密度以及黑质致密部(SNpc)和纹状体多巴胺能纤维中小胶质细胞和星形胶质细胞反应性的影响。
动物补充鱼油 50 天,并接受单侧纹状体 6-羟多巴胺(6-OHDA)诱导的损伤作为 PD 模型。
鱼油减轻了 6-OHDA 引起的 SNpc 神经元和纹状体神经末梢的丢失。这种保护作用与 iNOS-免疫反应细胞密度以及小胶质细胞和星形胶质细胞反应性的降低有关。
这些结果表明,鱼油补充的抗氧化和抗炎特性与 6-OHDA 诱导的 PD 模型引起的多巴胺能损伤的减少密切相关。