Kang Jun Mo, Park Hi Joon, Choi Yeong Gon, Choe Il Hwan, Park Jae Hyun, Kim Yong Sik, Lim Sabina
Department of Meridian and Acupoints, College of Korean Medicine, Kyung Hee University, Seoul, South Korea; WHO Collaborating Centre for Traditional Medicine, East-West Medical Research Institute, Kyung Hee University, Seoul, South Korea.
Brain Res. 2007 Feb 2;1131(1):211-9. doi: 10.1016/j.brainres.2006.10.089. Epub 2006 Dec 14.
Using a mouse model of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson's disease (PD), this study investigated on the neuroprotective effects of acupuncture by examining whether acupuncture contributed to inhibiting microglial activation and inflammatory events. C57BL/6 mice were treated with MPTP (30 mg/kg, i.p.) for 5 consecutive days. Acupuncture was then applied to acupoints Yanglingquan (GB34) and Taichong (LR3) starting 2 h after the first MPTP administration and then at 48 h intervals until the mice were sacrificed for analyses at 1, 3, and 7 days after the last MPTP injection. These experiments demonstrated that acupuncture inhibited the decreased of the tyrosine hydroxylase (TH) immunoreactivity (IR) and generated a neuroprotective effects in the striatum (ST) and the substantia nigra (SN) on days 1, 3, and 7 post-MPTP injections. Acupuncture attenuated the increase of macrophage antigen complex-1 (MAC-1), a marker of microglial activation, at 1 and 3 days and reduced the increases in cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression on days 1, 3, and 7. In MPTP group, striatal dopamine (DA) was measured by 46% at 7 days, whereas DA in the acupuncture group was 78%. On the basis of these results, we suggest that acupuncture could be used as a neuroprotective intervention for the purpose of inhibiting microglial activation and inflammatory events in PD.
本研究采用1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病(PD)小鼠模型,通过检测针刺是否有助于抑制小胶质细胞活化和炎症反应来研究针刺的神经保护作用。C57BL/6小鼠连续5天腹腔注射MPTP(30 mg/kg)。在首次注射MPTP后2小时开始针刺阳陵泉(GB34)和太冲(LR3)穴位,然后每隔48小时针刺一次,直至在最后一次注射MPTP后1、3和7天处死小鼠进行分析。这些实验表明,针刺可抑制酪氨酸羟化酶(TH)免疫反应性(IR)的降低,并在MPTP注射后第1、3和7天对纹状体(ST)和黑质(SN)产生神经保护作用。针刺在第1天和第3天减弱了小胶质细胞活化标志物巨噬细胞抗原复合物-1(MAC-1)的增加,并在第1、3和7天降低了环氧合酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)表达的增加。在MPTP组,7天时纹状体多巴胺(DA)水平下降了46%,而针刺组的DA水平为78%。基于这些结果,我们认为针刺可作为一种神经保护干预措施,用于抑制PD中的小胶质细胞活化和炎症反应。