Vagus Nerve Stimulation with Mild Stimulation Intensity Exerts Anti-Inflammatory and Neuroprotective Effects in Parkinson's Disease Model Rats

被引:25
作者
Kin, Ittetsu [1 ]
Sasaki, Tatsuya [1 ]
Yasuhara, Takao [1 ]
Kameda, Masahiro [1 ]
Agari, Takashi [2 ]
Okazaki, Mihoko [1 ]
Hosomoto, Kakeru [1 ]
Okazaki, Yosuke [1 ]
Yabuno, Satoru [1 ]
Kawauchi, Satoshi [1 ]
Kuwahara, Ken [1 ]
Morimoto, Jun [1 ]
Kin, Kyohei [1 ]
Umakoshi, Michiari [1 ]
Tomita, Yousuke [1 ]
Tajiri, Naoki [3 ,4 ,5 ]
Borlongan, Cesario, V [6 ]
Date, Isao [1 ]
机构
[1] Okayama Univ, Dept Neurol Surg, Grad Sch Med Dent & Pharmaceut Sci, Okayama 7008558, Japan
[2] Tokyo Metropolitan Neurol Hosp, Dept Neurosurg, Tokyo 1830042, Japan
[3] Nagoya City Univ, Dept Neurophysiol & Brain Sci, Nagoya, Aichi 4640083, Japan
[4] Nagoya City Univ, Med Sch, Grad Sch Med Sci, Nagoya, Aichi 4640083, Japan
[5] Nagoya City Univ, Med Sch, Nagoya, Aichi 4640083, Japan
[6] Univ S Florida, Dept Neurosurg & Brain Repair, Morsani Coll Med, 12901 Bruce B Downs Blvd, Tampa, FL 33611 USA
关键词
anti-inflammation; less invasive therapy; new experimental device; Parkinson's disease; vagus nerve stimulation; LOCUS-COERULEUS; ALZHEIMERS-DISEASE; FUNCTIONAL RECOVERY; SUBSTANTIA-NIGRA; PLASTICITY; NOREPINEPHRINE; NEUROINFLAMMATION; COMPLICATIONS; DYSFUNCTION; STROKE;
D O I
10.3390/biomedicines9070789
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The major surgical treatment for Parkinson's disease (PD) is deep brain stimulation (DBS), but a less invasive treatment is desired. Vagus nerve stimulation (VNS) is a relatively safe treatment without cerebral invasiveness. In this study, we developed a wireless controllable electrical stimulator to examine the efficacy of VNS on PD model rats. Methods: Adult female Sprague-Dawley rats underwent placement of a cuff-type electrode and stimulator on the vagus nerve. Following which, 6-hydroxydopamine (6-OHDA) was administered into the left striatum to prepare a PD model. VNS was started immediately after 6-OHDA administration and continued for 14 days. We evaluated the therapeutic effects of VNS with behavioral and immunohistochemical outcome assays under different stimulation intensity (0.1, 0.25, 0.5 and 1 mA). Results: VNS with 0.25-0.5 mA intensity remarkably improved behavioral impairment, preserved dopamine neurons, reduced inflammatory glial cells, and increased noradrenergic neurons. On the other hand, VNS with 0.1 mA and 1 mA intensity did not display significant therapeutic efficacy. Conclusions: VNS with 0.25-0.5 mA intensity has anti-inflammatory and neuroprotective effects on PD model rats induced by 6-OHDA administration. In addition, we were able to confirm the practicality and effectiveness of the new experimental device.
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页数:19
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