Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography. / Gjedde, Albert; Wong, Dean F. F.

In: Frontiers in Neuroscience, Vol. 16, 943512, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Gjedde, A & Wong, DFF 2022, 'Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography', Frontiers in Neuroscience, vol. 16, 943512. https://doi.org/10.3389/fnins.2022.943512

APA

Gjedde, A., & Wong, D. F. F. (2022). Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography. Frontiers in Neuroscience, 16, [943512]. https://doi.org/10.3389/fnins.2022.943512

Vancouver

Gjedde A, Wong DFF. Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography. Frontiers in Neuroscience. 2022;16. 943512. https://doi.org/10.3389/fnins.2022.943512

Author

Gjedde, Albert ; Wong, Dean F. F. / Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography. In: Frontiers in Neuroscience. 2022 ; Vol. 16.

Bibtex

@article{ff2f0293176b4d6ca8afe821d9215ccb,
title = "Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography",
abstract = "Decryption of brain images is the basis for the necessary translation of the findings from imaging to information required to meet the demands of clinical intervention. Tools of brain imaging, therefore, must satisfy the conditions dictated by the needs for interpretation in terms of diagnosis and prognosis. In addition, the applications must serve as fundamental research tools that enable the understanding of new therapeutic drugs, including compounds as diverse as antipsychotics, antidepressants, anxiolytics, and drugs serving the relief of symptoms from neurochemical disorders as unrelated as multiple sclerosis, stroke, and dementia. Here we review and explain the kinetics of methods that enable researchers to describe the brain's work and functions. We focus on methods invented by neurokineticists and expanded upon by practitioners during decades of experimental work and on the methods that are particularly useful to predict possible future approaches to the treatment of neurochemical disorders. We provide an overall description of the basic elements of kinetics and the underlying quantification methods, as well as the mathematics of modeling the recorded brain dynamics embedded in the images we obtain in vivo. The complex presentation to follow is necessary to justify the contribution of modeling to the development of methods and to support the specifications dictated by the proposed use in clinical settings. The quantification and kinetic modeling processes are equally essential to image reconstruction and labeling of brain regions of structural or functional interest. The procedures presented here are essential tools of scientific approaches to all conventional and novel forms of brain imaging. The foundations of the kinetic and quantitative methods are keys to the satisfaction of clinicians that actively engage in treating the neurochemical disorders of mammalian brains in the fields of neurology, neurosurgery, and neuropsychiatry.",
keywords = "neuroreceptor pet, kinetics, molecular neuroscience, neurotransmision, positron emission tomography, LIVING HUMAN-BRAIN, CEREBRAL GLUCOSE-UTILIZATION, DOPA DECARBOXYLASE ACTIVITY, BLOOD-FLOW, LUMPED CONSTANT, RECEPTOR OCCUPANCY, GRAPHICAL ANALYSIS, TOURETTE SYNDROME, BINDING, PET",
author = "Albert Gjedde and Wong, {Dean F. F.}",
year = "2022",
doi = "10.3389/fnins.2022.943512",
language = "English",
volume = "16",
journal = "Frontiers in Neuroscience",
issn = "1662-4548",
publisher = "Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Four decades of mapping and quantifying neuroreceptors at work in vivo by positron emission tomography

AU - Gjedde, Albert

AU - Wong, Dean F. F.

PY - 2022

Y1 - 2022

N2 - Decryption of brain images is the basis for the necessary translation of the findings from imaging to information required to meet the demands of clinical intervention. Tools of brain imaging, therefore, must satisfy the conditions dictated by the needs for interpretation in terms of diagnosis and prognosis. In addition, the applications must serve as fundamental research tools that enable the understanding of new therapeutic drugs, including compounds as diverse as antipsychotics, antidepressants, anxiolytics, and drugs serving the relief of symptoms from neurochemical disorders as unrelated as multiple sclerosis, stroke, and dementia. Here we review and explain the kinetics of methods that enable researchers to describe the brain's work and functions. We focus on methods invented by neurokineticists and expanded upon by practitioners during decades of experimental work and on the methods that are particularly useful to predict possible future approaches to the treatment of neurochemical disorders. We provide an overall description of the basic elements of kinetics and the underlying quantification methods, as well as the mathematics of modeling the recorded brain dynamics embedded in the images we obtain in vivo. The complex presentation to follow is necessary to justify the contribution of modeling to the development of methods and to support the specifications dictated by the proposed use in clinical settings. The quantification and kinetic modeling processes are equally essential to image reconstruction and labeling of brain regions of structural or functional interest. The procedures presented here are essential tools of scientific approaches to all conventional and novel forms of brain imaging. The foundations of the kinetic and quantitative methods are keys to the satisfaction of clinicians that actively engage in treating the neurochemical disorders of mammalian brains in the fields of neurology, neurosurgery, and neuropsychiatry.

AB - Decryption of brain images is the basis for the necessary translation of the findings from imaging to information required to meet the demands of clinical intervention. Tools of brain imaging, therefore, must satisfy the conditions dictated by the needs for interpretation in terms of diagnosis and prognosis. In addition, the applications must serve as fundamental research tools that enable the understanding of new therapeutic drugs, including compounds as diverse as antipsychotics, antidepressants, anxiolytics, and drugs serving the relief of symptoms from neurochemical disorders as unrelated as multiple sclerosis, stroke, and dementia. Here we review and explain the kinetics of methods that enable researchers to describe the brain's work and functions. We focus on methods invented by neurokineticists and expanded upon by practitioners during decades of experimental work and on the methods that are particularly useful to predict possible future approaches to the treatment of neurochemical disorders. We provide an overall description of the basic elements of kinetics and the underlying quantification methods, as well as the mathematics of modeling the recorded brain dynamics embedded in the images we obtain in vivo. The complex presentation to follow is necessary to justify the contribution of modeling to the development of methods and to support the specifications dictated by the proposed use in clinical settings. The quantification and kinetic modeling processes are equally essential to image reconstruction and labeling of brain regions of structural or functional interest. The procedures presented here are essential tools of scientific approaches to all conventional and novel forms of brain imaging. The foundations of the kinetic and quantitative methods are keys to the satisfaction of clinicians that actively engage in treating the neurochemical disorders of mammalian brains in the fields of neurology, neurosurgery, and neuropsychiatry.

KW - neuroreceptor pet

KW - kinetics

KW - molecular neuroscience

KW - neurotransmision

KW - positron emission tomography

KW - LIVING HUMAN-BRAIN

KW - CEREBRAL GLUCOSE-UTILIZATION

KW - DOPA DECARBOXYLASE ACTIVITY

KW - BLOOD-FLOW

KW - LUMPED CONSTANT

KW - RECEPTOR OCCUPANCY

KW - GRAPHICAL ANALYSIS

KW - TOURETTE SYNDROME

KW - BINDING

KW - PET

U2 - 10.3389/fnins.2022.943512

DO - 10.3389/fnins.2022.943512

M3 - Journal article

C2 - 36161158

VL - 16

JO - Frontiers in Neuroscience

JF - Frontiers in Neuroscience

SN - 1662-4548

M1 - 943512

ER -

ID: 321253948