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Repeated transcranial low-level laser therapy for traumatic brain injury in mice: biphasic dose response and long-term treatment outcome

机译:反复经颅低剂量激光治疗小鼠颅脑外伤:双相剂量反应和长期治疗结果

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摘要

We previously showed that near-infrared laser photobiomodulation (PBM) (810 nm, CW, 18 J/cm2, 25 mW/cm2) delivered to the mouse daily for 3-days after a controlled cortical impact traumatic brain injury (TBI) gave a significant improvement in neurological/cognitive function. However the same parameters delivered 14X daily gave significantly less benefit. This biphasic dose response intrigued us, and we decided to follow the mice that received 3X or 14X laser treatments out to 56-days post-TBI. We found the 14X group showed worse neurological function than the no-treatment TBI group at 2-weeks, but started to improve steadily during the next 6-weeks, and by 56-days were significantly better than the no-treatment TBI mice, but still worse than the 3X mice. A marker of activated glial cells (GFAP) was significantly increased in the brain regions (compared to both untreated TBI and 3X groups) at 4-weeks in the 14X group, but the GFAP had fallen to low levels in both 3X and 14X groups by 8-weeks. We conclude that an excessive number of laser-treatments delivered to mice can temporarily inhibit the process of brain repair stimulated by tPBM, but then the inhibitory effect ceases, and brain repair can resume. The mechanism may be temporary induction of reactive gliosis.
机译:我们先前显示每天向小鼠递送近红外激光光调制(PBM)(810 nm,CW,18 J / cm 2 ,25 mW / cm 2 )皮质撞击控制后3天,创伤性脑损伤(TBI)显着改善了神经/认知功能。但是,每天交付14倍的相同参数所产生的收益却大大减少。这种双相剂量反应引起了我们的兴趣,我们决定将接受3X或14X激光治疗的小鼠追踪到TBI后56天。我们发现14X组在2周时的神经功能比未治疗的TBI组差,但在接下来的6周中开始稳定地改善,到56天时显着优于未治疗的TBI小鼠,但是仍然比3X小鼠差。 14X组在第4周时,神经胶质细胞(GFAP)的标记在4周时在大脑区域显着增加(与未治疗的TBI和3X组相比),但到3X和14X组,GFAP均降至低水平8周。我们得出的结论是,对小鼠进行过多的激光治疗可以暂时抑制tPBM刺激的脑修复过程,但随后抑制作用停止,脑修复可以恢复。其机制可能是暂时性反应性神经胶质增生。

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