Low level laser therapy for traumatic brain injury

Low level laser (or light) therapy (LLLT) has been clinically applied for many indications in medicine that require the following processes: protection from cell and tissue death, stimulation of healing and repair of injuries, and reduction of pain, swelling and inflammation. One area that is attracting growing interest is the use of transcranial LLLT to treat stroke and traumatic brain injury (TBI). The fact that near-infrared light can penetrate into the brain would allow non-invasive treatment to be carried out with a low likelihood of treatment-related adverse events. LLLT may have beneficial effects in the acute treatment of brain damage injury by increasing respiration in the mitochondria, causing activation of transcription factors, reducing key inflammatory mediators, and inhibiting apoptosis. We tested LLLT in a mouse model of TBI produced by a controlled weight drop onto the skull. Mice received a single treatment with 660-nm, 810-nm or 980-nm laser (36 J/cm2) four hours post-injury and were followed up by neurological performance testing for 4 weeks. Mice with moderate to severe TBI treated with 660- nm and 810-nm laser had a significant improvement in neurological score over the course of the follow-up and histological examination of the brains at sacrifice revealed less lesion area compared to untreated controls. Further studies are underway.

[1]  Marc Fisher,et al.  Infrared Laser Therapy for Ischemic Stroke: A New Treatment Strategy: Results of the NeuroThera Effectiveness and Safety Trial–1 (NEST-1) , 2007, Stroke.

[2]  T. Karu Mitochondrial Signaling in Mammalian Cells Activated by Red and Near‐IR Radiation , 2008, Photochemistry and photobiology.

[3]  David K Menon,et al.  Traumatic brain injury: physiology, mechanisms, and outcome , 2004, Current opinion in neurology.

[4]  Nick Lane,et al.  Power games , 2006 .

[5]  Michael R. Hamblin,et al.  Low-Level Laser Therapy in Stroke and Central Nervous System , 2010 .

[6]  T. Karu,et al.  Absorption measurements of a cell monolayer relevant to phototherapy: reduction of cytochrome c oxidase under near IR radiation. , 2005, Journal of photochemistry and photobiology. B, Biology.

[7]  Amir Oron,et al.  low-level laser therapy applied transcranially to mice following traumatic brain injury significantly reduces long-term neurological deficits. , 2007, Journal of neurotrauma.

[8]  Michael R. Hamblin,et al.  Advances in Low-Intensity Laser and Phototherapy , 2010 .

[9]  J. Ghajar,et al.  In Reply: Guidelines for the Management of Severe Traumatic Brain Injury: 2020 Update of the Decompressive Craniectomy Recommendations. , 2020, Neurosurgery.

[10]  Michael R. Hamblin,et al.  Mechanisms of low level light therapy , 2006, SPIE BiOS.

[11]  S. Michalikova,et al.  Emotional responses and memory performance of middle-aged CD1 mice in a 3D maze: Effects of low infrared light , 2008, Neurobiology of Learning and Memory.

[12]  Britton Chance,et al.  Photobiomodulation Directly Benefits Primary Neurons Functionally Inactivated by Toxins , 2005, Journal of Biological Chemistry.

[13]  J. Povlishock,et al.  Guidelines for the management of severe traumatic brain injury. Editor's Commentary. , 2007, Journal of neurotrauma.

[14]  L. Klimaschewski,et al.  From Birth Till Death: Neurogenesis, Cell Cycle, and Neurodegeneration , 2009, Anatomical record.