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超声触发的微泡联合载有胶质细胞源性神经营养因子(GDNF)质粒的聚乙二醇化脂质体在帕金森病大鼠模型中的作用

Ultrasound-Triggered Effects of the Microbubbles Coupled to GDNF Plasmid-Loaded PEGylated Liposomes in a Rat Model of Parkinson's Disease.

作者信息

Yue Peijian, Miao Wang, Gao Lin, Zhao Xinyu, Teng Junfang

机构信息

Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Department of Neurological Intensive Care Unit, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Neurosci. 2018 Apr 6;12:222. doi: 10.3389/fnins.2018.00222. eCollection 2018.

Abstract

The purpose of this study was to investigate ultrasound-triggered effects of PEGylated liposomes-coupled microbubbles mediated gene transfer of glial cell line-derived neurotrophic factor (GDNF) plasmid (PLs-GDNF-MBs) on behavioral deficits and neuron loss in a rat model of Parkinson's disease (PD). The unloaded PLs-MBs were characterized for particle size, concentration and zeta potential. PD rat model was established by a unilateral 6-hydroxydopamine (6-OHDA) lesion. Rotational, climbing pole, and suspension tests were used to evaluate behavioral deficits. The immunohistochemical staining of tyrosine hydroxylase (TH) and dopamine transporter (DAT) was used to assess the neuron loss. The expression levels of GDNF and nuclear receptor-related factor 1 (Nurr1) were determined by western blot and qRT-PCR analysis. The particle size of PLs-MBs was gradually increased, while the concentration and absolute zeta potential were gradually decreased in a time-dependent manner after injection. 6-OHDA elevated amphetamine-induced rotations and decreased the TH and DAT immunoreactivity compared to sham group. However, these effects were blocked by the PLs-GDNF-MBs. In addition, the mRNA and protein expression levels of GDNF and Nurr1 were increased after PLs-GDNF-MBs treatment. The delivery of PLs-GDNF-MBs into the brains using MRI-guided focused ultrasound alleviates the behavioral deficits and neuron loss in the rat model of PD.

摘要

本研究的目的是探讨聚乙二醇化脂质体偶联微泡介导的胶质细胞源性神经营养因子(GDNF)质粒(PLs-GDNF-MBs)基因转移在帕金森病(PD)大鼠模型中对行为缺陷和神经元丢失的超声触发效应。对未负载的PLs-MBs进行粒径、浓度和zeta电位表征。通过单侧6-羟基多巴胺(6-OHDA)损伤建立PD大鼠模型。采用旋转、爬杆和悬吊试验评估行为缺陷。用酪氨酸羟化酶(TH)和多巴胺转运体(DAT)的免疫组织化学染色评估神经元丢失。通过蛋白质免疫印迹和qRT-PCR分析测定GDNF和核受体相关因子1(Nurr1)的表达水平。注射后,PLs-MBs的粒径逐渐增大,而浓度和绝对zeta电位呈时间依赖性逐渐降低。与假手术组相比,6-OHDA增加了苯丙胺诱导的旋转,并降低了TH和DAT免疫反应性。然而,这些效应被PLs-GDNF-MBs阻断。此外,PLs-GDNF-MBs治疗后GDNF和Nurr1的mRNA和蛋白表达水平升高。使用MRI引导聚焦超声将PLs-GDNF-MBs递送至大脑可减轻PD大鼠模型中的行为缺陷和神经元丢失。

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