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神经营养因子缀合纳米颗粒可预防氧化应激诱导的视网膜损伤。

Neurotrophin-conjugated nanoparticles prevent retina damage induced by oxidative stress.

机构信息

Department of Biology, Università di Pisa, 56127, Pisa, Italy.

Department of Chemistry and Industrial Chemistry, Università di Pisa, 56124, Pisa, Italy.

出版信息

Cell Mol Life Sci. 2018 Apr;75(7):1255-1267. doi: 10.1007/s00018-017-2691-x. Epub 2017 Nov 2.

Abstract

Glaucoma and other optic neuropathies are characterized by a loss of retinal ganglion cells (RGCs), a cell layer located in the posterior eye segment. Several preclinical studies demonstrate that neurotrophins (NTs) prevent RGC loss. However, NTs are rarely investigated in the clinic due to various issues, such as difficulties in reaching the retina, the very short half-life of NTs, and the need for multiple injections. We demonstrate that NTs can be conjugated to magnetic nanoparticles (MNPs), which act as smart drug carriers. This combines the advantages of the self-localization of the drug in the retina and drug protection from fast degradation. We tested the nerve growth factor and brain-derived neurotrophic factor by comparing the neuroprotection of free versus conjugated proteins in a model of RGC loss induced by oxidative stress. Histological data demonstrated that the conjugated proteins totally prevented RGC loss, in sharp contrast to the equivalent dose of free proteins, which had no effect. The overall data suggest that the nanoscale MNP-protein hybrid is an excellent tool in implementing ocular drug delivery strategies for neuroprotection and therapy.

摘要

青光眼和其他视神经病变的特征是视网膜神经节细胞 (RGC) 的丧失,RGC 位于眼球后段。几项临床前研究表明神经营养因子 (NT) 可防止 RGC 丢失。然而,由于各种问题,NT 在临床上很少被研究,例如难以到达视网膜、NT 的半衰期非常短以及需要多次注射。我们证明 NT 可以与磁性纳米颗粒 (MNP) 结合,后者可以作为智能药物载体。这结合了药物在视网膜中的自我定位和药物免受快速降解的优势。我们通过比较氧化应激诱导的 RGC 损失模型中游离蛋白和共轭蛋白的神经保护作用来测试神经生长因子和脑源性神经营养因子。组织学数据表明,与等效剂量的无作用游离蛋白相比,共轭蛋白完全阻止了 RGC 的丢失。总体数据表明,纳米级 MNP-蛋白杂交物是实施神经保护和治疗眼部药物输送策略的极好工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ecc/11105483/0b3279558b60/18_2017_2691_Fig1_HTML.jpg

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