Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain

Research output: Contribution to journalReviewResearchpeer-review

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Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain. / Fernandes, Eduardo Felipe Alves; Ozcelik, Dennis.

In: Antioxidants, Vol. 10, No. 4, 528, 2021.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Fernandes, EFA & Ozcelik, D 2021, 'Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain', Antioxidants, vol. 10, no. 4, 528. https://doi.org/10.3390/antiox10040528

APA

Fernandes, E. F. A., & Ozcelik, D. (2021). Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain. Antioxidants, 10(4), [528]. https://doi.org/10.3390/antiox10040528

Vancouver

Fernandes EFA, Ozcelik D. Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain. Antioxidants. 2021;10(4). 528. https://doi.org/10.3390/antiox10040528

Author

Fernandes, Eduardo Felipe Alves ; Ozcelik, Dennis. / Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain. In: Antioxidants. 2021 ; Vol. 10, No. 4.

Bibtex

@article{08e2865df23148358fdf7c8bfa9c41c8,
title = "Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain",
abstract = "Inflammation is one key process in driving cellular redox homeostasis toward oxidative stress, which perpetuates inflammation. In the brain, this interplay results in a vicious cycle of cell death, the loss of neurons, and leakage of the blood-brain barrier. Hence, the neuroinflammatory response fuels the development of acute and chronic inflammatory diseases. Interrogation of the interplay between inflammation, oxidative stress, and cell death in neurological tissue in vivo is very challenging. The complexity of the underlying biological process and the fragility of the brain limit our understanding of the cause and the adequate diagnostics of neuroinflammatory diseases. In recent years, advancements in the development of molecular imaging agents addressed this limitation and enabled imaging of biomarkers of neuroinflammation in the brain. Notable redox biomarkers for imaging with positron emission tomography (PET) tracers are the 18 kDa translocator protein (TSPO) and monoamine oxygenase B (MAO-B). These findings and achievements offer the opportunity for novel diagnostic applications and therapeutic strategies. This review summarizes experimental as well as established pharmaceutical and biotechnological tools for imaging the inflammatory redox landscape in the brain, and provides a glimpse into future applications.",
keywords = "oxidative stress response, reactive oxygen species, imaging biomarker, redox sensor, microglia, positron emission tomography, TSPO, MAO&#8211, B",
author = "Fernandes, {Eduardo Felipe Alves} and Dennis Ozcelik",
year = "2021",
doi = "10.3390/antiox10040528",
language = "English",
volume = "10",
journal = "Antioxidants",
issn = "2076-3921",
publisher = "M D P I AG",
number = "4",

}

RIS

TY - JOUR

T1 - Imaging Biomarkers for Monitoring the Inflammatory Redox Landscape in the Brain

AU - Fernandes, Eduardo Felipe Alves

AU - Ozcelik, Dennis

PY - 2021

Y1 - 2021

N2 - Inflammation is one key process in driving cellular redox homeostasis toward oxidative stress, which perpetuates inflammation. In the brain, this interplay results in a vicious cycle of cell death, the loss of neurons, and leakage of the blood-brain barrier. Hence, the neuroinflammatory response fuels the development of acute and chronic inflammatory diseases. Interrogation of the interplay between inflammation, oxidative stress, and cell death in neurological tissue in vivo is very challenging. The complexity of the underlying biological process and the fragility of the brain limit our understanding of the cause and the adequate diagnostics of neuroinflammatory diseases. In recent years, advancements in the development of molecular imaging agents addressed this limitation and enabled imaging of biomarkers of neuroinflammation in the brain. Notable redox biomarkers for imaging with positron emission tomography (PET) tracers are the 18 kDa translocator protein (TSPO) and monoamine oxygenase B (MAO-B). These findings and achievements offer the opportunity for novel diagnostic applications and therapeutic strategies. This review summarizes experimental as well as established pharmaceutical and biotechnological tools for imaging the inflammatory redox landscape in the brain, and provides a glimpse into future applications.

AB - Inflammation is one key process in driving cellular redox homeostasis toward oxidative stress, which perpetuates inflammation. In the brain, this interplay results in a vicious cycle of cell death, the loss of neurons, and leakage of the blood-brain barrier. Hence, the neuroinflammatory response fuels the development of acute and chronic inflammatory diseases. Interrogation of the interplay between inflammation, oxidative stress, and cell death in neurological tissue in vivo is very challenging. The complexity of the underlying biological process and the fragility of the brain limit our understanding of the cause and the adequate diagnostics of neuroinflammatory diseases. In recent years, advancements in the development of molecular imaging agents addressed this limitation and enabled imaging of biomarkers of neuroinflammation in the brain. Notable redox biomarkers for imaging with positron emission tomography (PET) tracers are the 18 kDa translocator protein (TSPO) and monoamine oxygenase B (MAO-B). These findings and achievements offer the opportunity for novel diagnostic applications and therapeutic strategies. This review summarizes experimental as well as established pharmaceutical and biotechnological tools for imaging the inflammatory redox landscape in the brain, and provides a glimpse into future applications.

KW - oxidative stress response

KW - reactive oxygen species

KW - imaging biomarker

KW - redox sensor

KW - microglia

KW - positron emission tomography

KW - TSPO

KW - MAO&#8211

KW - B

U2 - 10.3390/antiox10040528

DO - 10.3390/antiox10040528

M3 - Review

C2 - 33800685

VL - 10

JO - Antioxidants

JF - Antioxidants

SN - 2076-3921

IS - 4

M1 - 528

ER -

ID: 262800034