Neuropsychopharmacology and Toxicology Program, BK21 PLUS Project, College of Pharmacy, Kangwon National University, Chunchon 24341, Korea.
College of Forest and Environmental Sciences, Kangwon National University, Chunchon 24341, Korea.
Curr Neuropharmacol. 2019;17(10):990-1002. doi: 10.2174/1570159X17666190228114318.
Far-infrared ray (FIR) is an electromagnetic wave that produces various health benefits against pathophysiological conditions, such as diabetes mellitus, renocardiovascular disorders, stress, and depression etc. However, the therapeutic application on the FIR-mediated protective potentials remains to be further extended. To achieve better understanding on FIR-mediated therapeutic potentials, we summarized additional findings in the present study that exposure to FIR ameliorates stressful condition, memory impairments, drug dependence, and mitochondrial dysfunction in the central nervous system. In this review, we underlined that FIR requires modulations of janus kinase 2 / signal transducer and activator of transcription 3 (JAK2/STAT3), nuclear factor E2- related factor 2 (Nrf-2), muscarinic M1 acetylcholine receptor (M1 mAChR), dopamine D1 receptor, protein kinase C δ gene, and glutathione peroxidase-1 gene for exerting the protective potentials in response to neuropsychotoxic conditions.
远红外射线(FIR)是一种电磁波,它可以针对糖尿病、心肾血管疾病、压力和抑郁等病理生理状况产生各种健康益处。然而,FIR 介导的保护潜能的治疗应用仍有待进一步扩展。为了更好地理解 FIR 介导的治疗潜力,我们在本研究中总结了其他发现,即暴露于 FIR 可改善中枢神经系统的应激状态、记忆障碍、药物依赖和线粒体功能障碍。在这篇综述中,我们强调 FIR 需要调节 Janus 激酶 2/信号转导和转录激活因子 3(JAK2/STAT3)、核因子 E2 相关因子 2(Nrf-2)、毒蕈碱 M1 乙酰胆碱受体(M1 mAChR)、多巴胺 D1 受体、蛋白激酶 C δ 基因和谷胱甘肽过氧化物酶-1 基因,以发挥针对神经毒性条件的保护潜能。