Wang Xiaoying, Cui Guiyun, Yang Xinxin, Zhang Zunsheng, Shi Hongjuan, Zu Jie, Hua Fang, Shen Xia
Department of Ultrasound, Affiliated Hospital of Xuzhou Medical College, PR China.
Department of Neurology, Affiliated Hospital of Xuzhou Medical College, PR China.
Brain Res Bull. 2014 Apr;103:60-5. doi: 10.1016/j.brainresbull.2014.02.006. Epub 2014 Feb 26.
Parkinson's disease (PD) is a neurodegenerative disease characterized by loss of dopaminergic neurons in the substantia nigra. Neurotrophic factors, such as glial cell derived neurotrophic factor (GDNF), have been shown to provide a neuroprotective effect in PD rats. We have previously reported that ultrasound-induced lipid-coated GDNF microspheres, which release GDNF in a sustained manner after low frequency ultrasound stimulation, can reduce hypoxic-ischemic injury in neonatal rats. In the present study, we investigated whether lipid-coated GDNF microspheres can provide a neuroprotective effect in a rat model of PD. After a rat model of PD was produced by 6-hydroxydompamine (6-OHDA) injections, lipid-coated GDNF microspheres (1.5mg/kg) were injected into the striatum of PD rats. We found that GDNF levels were increased in the striatum of PD rats after lipid-coated GDNF microspheres administration following low frequency ultrasound stimulation (20kHz, 5min per day, daily for 4 weeks). Moreover, GDNF microspheres reduced apomorphine-induced rotations, and increased striatal dopamine and nigral tyrosine hydroxylase (TH) levels in PD rats. Additionally, GDNF microspheres reduced caspase-3, tumor necrosis factor-alpha, matrix metalloproteinase 9 (MMP-9) and OX-6 levels induced by 6-OHDA injections in PD rats. These data indicated that lipid-coated GDNF microspheres can provide a neuroprotective effect in PD rats.
帕金森病(PD)是一种神经退行性疾病,其特征是黑质中多巴胺能神经元丧失。神经营养因子,如胶质细胞源性神经营养因子(GDNF),已被证明在帕金森病大鼠中具有神经保护作用。我们之前报道过,超声诱导的脂质包裹的GDNF微球在低频超声刺激后能持续释放GDNF,可减轻新生大鼠的缺氧缺血性损伤。在本研究中,我们调查了脂质包裹的GDNF微球是否能在帕金森病大鼠模型中发挥神经保护作用。通过注射6-羟基多巴胺(6-OHDA)建立帕金森病大鼠模型后,将脂质包裹的GDNF微球(1.5mg/kg)注射到帕金森病大鼠的纹状体中。我们发现,在低频超声刺激(20kHz,每天5分钟,持续4周)后给予脂质包裹的GDNF微球,帕金森病大鼠纹状体中的GDNF水平升高。此外,GDNF微球减少了阿扑吗啡诱导的旋转,并提高了帕金森病大鼠纹状体多巴胺和黑质酪氨酸羟化酶(TH)水平。另外,GDNF微球降低了6-OHDA注射诱导的帕金森病大鼠中caspase-3、肿瘤坏死因子-α、基质金属蛋白酶9(MMP-9)和OX-6水平。这些数据表明,脂质包裹的GDNF微球可在帕金森病大鼠中发挥神经保护作用。