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首页> 外文期刊>レ-ザ-研究 >低出力光の中枢神経疾患治療ヘの応用:拡延性脱分極の制御
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低出力光の中枢神経疾患治療ヘの応用:拡延性脱分極の制御

机译:低功率光在中枢神经系统疾病治疗中的应用:扩散去极化的控制

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摘要

Anoxic depolarization (AD),which is caused by ischemia/hypoxia in brain, is known to trigger neuronal cell death. Energy restoration would be needed for preventing the occurrence of AD and resultant cell death. Photobiomodulation therapy, in which low-intensity light with a specific wavelength is used for mitochondria, can enhance energy production in neuronal cells under pathophysiological conditions. In this study, we examined whether visible (665 nm) or near-infrared (808 nm) laser irradiation can control the occurrence of AD in rat brain. At both wavelengths, the onset of AD was significantly delayed in the light-treated hemisphere when compared with that in the non-treated hemisphere (n=8). The spreading area of AD was also significantly smaller in the light-treated hemisphere than in the non-treated hemisphere. These results suggest that photobiomodulation therapy can control AD in the brain, which is probably due to an increase in ATP by laser irradiation.
机译:已知由脑缺血/缺氧引起的缺氧去极化(AD)会触发神经元细胞死亡。需要能量恢复来防止AD的发生和由此导致的细胞死亡。光生物调节疗法可将特定波长的低强度光用于线粒体,从而增强病理生理条件下神经元细胞的能量产生。在这项研究中,我们检查了可见(665 nm)或近红外(808 nm)激光照射能否控制大鼠大脑中AD的发生。在两个波长下,与未处理的半球相比,在光处理的半球中AD的发作显着延迟(n = 8)。在光处理的半球中,AD的扩散面积也显着小于未处理的半球。这些结果表明,光生物调节疗法可以控制大脑中的AD,这可能是由于激光照射使ATP增加所致。

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