Kim Jin Hee, Choi Yujin, Kim Jin Se, Lee Hanbyeol, Ju In Gyoung, Yoo Na Young, La Sookie, Jeong Do Hyeon, Na Changsu, Park Hi-Joon, Oh Myung Sook
Department of Biomedical and Pharmaceutical Sciences, Kyung Hee University, Seoul, Republic of Korea.
Department of Oriental Pharmaceutical Science and Kyung Hee East-West Pharmaceutical Research Institute, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea.
Front Immunol. 2024 Nov 19;15:1454102. doi: 10.3389/fimmu.2024.1454102. eCollection 2024.
Immune dysfunction is a major cause of neuroinflammation and accelerates the progression of Parkinson's disease (PD). Numerous studies have shown that stimulation of specific acupuncture points (acupoints) can ameliorate PD symptoms. The purpose of this study was to investigate whether attaching microneedles to acupoints would improve PD pathology by recovering immune dysfunction.
The PD mouse model was induced by intrastriatal injection of 6-hydroxydopamine (6-OHDA), and microneedle patches (MPs) or sham patches (SPs) were attached to GB20 and GB34, representative acupoints for treating PD for 14 days.
First, the behavioral experiment showed that motor disorders induced by 6-OHDA were significantly improved by MP. Simultaneously, 6-OHDA-induced dopaminergic neuronal death and brain neuroinflammation decreased. Conversely, SP had no effect on behavioral disorders, neuronal death, or neuroinflammation. Measurement results from flow cytometry of immune cells in the brain and blood revealed a disruption in the CD4+/CD8+ ratio in the 6-OHDA group, which was significantly restored in the MP group. The brain mRNA expression of cytokines was significantly increased in the 6-OHDA group, which was significantly decreased by MP.
Overall, our results suggest that the attachment of MPs to GB20 and GB34 is a new method to effectively improve the pathology of PD by restoring peripheral and brain immune function.
免疫功能障碍是神经炎症的主要原因,并加速帕金森病(PD)的进展。大量研究表明,刺激特定穴位可改善PD症状。本研究旨在探讨在穴位上贴附微针是否能通过恢复免疫功能障碍来改善PD病理。
通过纹状体内注射6-羟基多巴胺(6-OHDA)诱导建立PD小鼠模型,将微针贴片(MPs)或假贴片(SPs)贴于治疗PD的代表性穴位GB20和GB34上,持续14天。
首先,行为学实验表明,MP可显著改善6-OHDA诱导的运动障碍。同时,6-OHDA诱导的多巴胺能神经元死亡和脑内神经炎症减少。相反,SP对行为障碍、神经元死亡或神经炎症无影响。对脑和血液中免疫细胞的流式细胞术测量结果显示,6-OHDA组的CD4+/CD8+比值紊乱,而MP组显著恢复。6-OHDA组脑内细胞因子的mRNA表达显著增加,而MP使其显著降低。
总体而言,我们的结果表明,在GB20和GB34穴位上贴附MPs是一种通过恢复外周和脑免疫功能有效改善PD病理的新方法。