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 inMolecular neurobiology Vol. 55; no. 8; pp. 6601 - 6636
Main Authors Salehpour, Farzad, Mahmoudi, Javad, Kamari, Farzin, Sadigh-Eteghad, Saeed, Rasta, Seyed Hossein, Hamblin, Michael R
Format Journal Article
LanguageEnglish
Published New York Springer US 01.08.2018
Springer Nature B.V
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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.
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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Photobiomodulation therapy
Stroke
Traumatic brain injury
Cortical neurons
Depression
Brain function
Dementia
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Snippet Brain photobiomodulation (PBM) therapy using red to near-infrared (NIR) light is an innovative treatment for a wide range of neurological and psychological...
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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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Title Brain Photobiomodulation Therapy: a Narrative Review
URI https://link.springer.com/article/10.1007/s12035-017-0852-4
https://www.ncbi.nlm.nih.gov/pubmed/29327206
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Volume 55
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