Wang Yuhong, Luo Kaixuan, Li Junrui, Liao Yehui, Liao Chengde, Chen Wen-Shiang, Chen Moxian, Ao Lijuan
School of Rehabilitation, Kunming Medical University, Kunming, China.
Yunnan Cancer Center, Department of Radiology, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Front Cell Neurosci. 2022 May 17;16:884788. doi: 10.3389/fncel.2022.884788. eCollection 2022.
Parkinson's disease (PD) is the second most common chronic neurodegenerative disease globally; however, it lacks effective treatment at present. Focused ultrasound (FUS) combined with microbubbles could increase the efficacy of drug delivery to specific brain regions and is becoming a promising technology for the treatment of central nervous system diseases. In this study, we explored the therapeutic potential of FUS-mediated blood-brain barrier (BBB) opening of the left striatum to deliver gastrodin (GAS) in a subacute PD mouse model induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). The concentration of GAS in the left hemisphere was detected by ultra-high performance liquid chromatography electrospray Q-Orbitrap mass spectrometry (UHPLC/ESI Q-Orbitrap) and the distribution of tyrosine hydroxylase (TH) neurons was detected by immunohistochemical staining. The expression of TH, Dopamine transporter (DAT), cleaved-caspase-3, B-cell lymphoma 2 (Bcl-2), brain-derived neurotrophic factor (BDNF), postsynaptic density protein 95 (PSD-95), and synaptophysin (SYN) protein were detected by western blotting. Analysis showed that the concentration of GAS in the left hemisphere of PD mice increased by approximately 1.8-fold after the BBB was opened. FUS-mediated GAS delivery provided optimal neuroprotective effects and was superior to the GAS or FUS control group. In addition, FUS enhanced GAS delivery significantly increased the expression of Bcl-2, BDNF, PSD-95, and SYN protein in the left striatum ( < 0.05) and reduced the levels of cleaved-caspase-3 remarkably ( = 0.001). In conclusion, the enhanced delivery by FUS effectively strengthened the protective effect of GAS on dopaminergic neurons which may be related to the reinforcement of the anti-apoptotic activity and the expression of synaptic-related proteins in the striatum. Data suggests that FUS-enhanced GAS delivery may represent a new strategy for PD treatment.
帕金森病(PD)是全球第二常见的慢性神经退行性疾病;然而,目前它缺乏有效的治疗方法。聚焦超声(FUS)联合微泡可提高药物向特定脑区的递送效率,正成为治疗中枢神经系统疾病的一项有前景的技术。在本研究中,我们在1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的亚急性PD小鼠模型中,探索了FUS介导的左侧纹状体血脑屏障(BBB)开放以递送天麻素(GAS)的治疗潜力。通过超高效液相色谱电喷雾Q-轨道阱质谱(UHPLC/ESI Q-轨道阱)检测左侧半球GAS的浓度,通过免疫组织化学染色检测酪氨酸羟化酶(TH)神经元的分布。通过蛋白质印迹法检测TH、多巴胺转运体(DAT)、裂解的半胱天冬酶-3、B细胞淋巴瘤2(Bcl-2)、脑源性神经营养因子(BDNF)、突触后密度蛋白95(PSD-95)和突触素(SYN)蛋白的表达。分析表明,BBB开放后,PD小鼠左侧半球GAS的浓度增加了约1.8倍。FUS介导的GAS递送提供了最佳的神经保护作用,优于GAS或FUS对照组。此外,FUS增强GAS递送显著增加了左侧纹状体中Bcl-2、BDNF、PSD-95和SYN蛋白的表达(<0.05),并显著降低了裂解的半胱天冬酶-3的水平(=0.001)。总之,FUS增强递送有效地增强了GAS对多巴胺能神经元的保护作用,这可能与增强抗凋亡活性和纹状体中突触相关蛋白的表达有关。数据表明,FUS增强GAS递送可能代表一种治疗PD的新策略。