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J Biophotonics. 2016 Dec;9(11-12):1263-1272. doi: 10.1002/jbio.201500336. Epub 2016 Mar 15.

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

Xuan W1,2,3, Huang L2,3, Hamblin MR2,3,4.

Author information

1
Dept of Otorhinolaryngology, Head and Neck Surgery, Ruikang Clinical Medical College, Guangxi University of Chinese Medicine, Nanning, China.
2
Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USA.
3
Department of Dermatology, Harvard Medical School, Boston, MA 02115, USA.
4
Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139, USA.

Abstract

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.

KEYWORDS:

LLLT; Morris water maze; Traumatic brain injury; biphasic dose response; controlled cortical impact mouse model; glial fibrillary acidic protein; photobiomodulation; reactive gliosis

PMID:
26990361
PMCID:
PMC5025344
DOI:
10.1002/jbio.201500336
[Indexed for MEDLINE]
Free PMC Article

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