Brain Photobiomodulation Therapy: a Narrative Review
Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthes...
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Published in | Molecular neurobiology Vol. 55; no. 8; pp. 6601 - 6636 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.08.2018
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Abstract | Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca
2+
and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson’s disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy. |
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AbstractList | Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca2+ and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson’s disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy. Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson's disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy. Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca2+ and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson's disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy.Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca2+ and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson's disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy. Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological conditions. Red/NIR light is able to stimulate complex IV of the mitochondrial respiratory chain (cytochrome c oxidase) and increase ATP synthesis. Moreover, light absorption by ion channels results in release of Ca 2+ and leads to activation of transcription factors and gene expression. Brain PBM therapy enhances the metabolic capacity of neurons and stimulates anti-inflammatory, anti-apoptotic, and antioxidant responses, as well as neurogenesis and synaptogenesis. Its therapeutic role in disorders such as dementia and Parkinson’s disease, as well as to treat stroke, brain trauma, and depression has gained increasing interest. In the transcranial PBM approach, delivering a sufficient dose to achieve optimal stimulation is challenging due to exponential attenuation of light penetration in tissue. Alternative approaches such as intracranial and intranasal light delivery methods have been suggested to overcome this limitation. This article reviews the state-of-the-art preclinical and clinical evidence regarding the efficacy of brain PBM therapy. |
Author | Rasta, Seyed Hossein Sadigh-Eteghad, Saeed Hamblin, Michael R Salehpour, Farzad Kamari, Farzin Mahmoudi, Javad |
AuthorAffiliation | a Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran b Department of Medical Physics, Tabriz University of Medical Sciences, Tabriz, Iran c Department of Medical Bioengineering, Tabriz University of Medical Sciences, Tabriz, Iran e Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts 02114, United States f Department of Dermatology, Harvard Medical School, Boston, Massachusetts 02115, United States g Harvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts 02139, United States d School of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom |
AuthorAffiliation_xml | – name: c Department of Medical Bioengineering, Tabriz University of Medical Sciences, Tabriz, Iran – name: g Harvard-MIT Division of Health Sciences and Technology, Cambridge, Massachusetts 02139, United States – name: b Department of Medical Physics, Tabriz University of Medical Sciences, Tabriz, Iran – name: f Department of Dermatology, Harvard Medical School, Boston, Massachusetts 02115, United States – name: a Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Tabriz, Iran – name: d School of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom – name: e Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts 02114, United States |
Author_xml | – sequence: 1 givenname: Farzad surname: Salehpour fullname: Salehpour, Farzad email: farzadsalehpour1988@gmail.com organization: Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences, Department of Medical Physics, Tabriz University of Medical Sciences – sequence: 2 givenname: Javad surname: Mahmoudi fullname: Mahmoudi, Javad organization: Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences – sequence: 3 givenname: Farzin surname: Kamari fullname: Kamari, Farzin organization: Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences – sequence: 4 givenname: Saeed surname: Sadigh-Eteghad fullname: Sadigh-Eteghad, Saeed organization: Neurosciences Research Center (NSRC), Tabriz University of Medical Sciences – sequence: 5 givenname: Seyed Hossein surname: Rasta fullname: Rasta, Seyed Hossein organization: Department of Medical Physics, Tabriz University of Medical Sciences, Department of Medical Bioengineering, Tabriz University of Medical Sciences, School of Medical Sciences, University of Aberdeen – sequence: 6 givenname: Michael R orcidid: 0000-0001-6431-4605 surname: Hamblin fullname: Hamblin, Michael R email: hamblin@helix.mgh.harvard.edu organization: Wellman Center for Photomedicine, Massachusetts General Hospital, Department of Dermatology, Harvard Medical School, Harvard-MIT Division of Health Sciences and Technology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29327206$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Animals Antioxidants Apoptosis Biomedical and Life Sciences Biomedicine Brain - pathology Calcium Cell Biology Cytochrome-c oxidase Dementia disorders Dose-Response Relationship, Radiation Electron transport Gene expression Humans I.R. radiation Inflammation Ion channels Light Light penetration Light therapy Low-Level Light Therapy Mitochondria Neurobiology Neurogenesis Neurology Neurosciences Oxidative Stress Stroke Synaptogenesis Transcription activation Transcription factors Traumatic brain injury |
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