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Molecular Imaging of Central Dopamine in Obesity: A Qualitative Review across Substrates and Radiotracers

期刊

BRAIN SCIENCES
卷 12, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/brainsci12040486

关键词

dopamine; obesity; BMI; Positron Emission Tomography; single-photon emission tomography

资金

  1. Bundesland Sachsen-Anhalt
  2. European Structure Fund

向作者/读者索取更多资源

Dopamine plays a crucial role in adaptive behavior, with obesity-related alterations affecting the central dopamine system, as shown in molecular neuroimaging studies. While there are associations between obesity and substrates of the dopamine system in humans, it is unlikely that obesity can be traced back to a single dopaminergic cause.
Dopamine is a neurotransmitter that plays a crucial role in adaptive behavior. A wealth of studies suggests obesity-related alterations in the central dopamine system. The most direct evidence for such differences in humans comes from molecular neuroimaging studies using positron emission tomography (PET) and single-photon emission computed tomography (SPECT). The aim of the current review is to give a comprehensive overview of molecular neuroimaging studies that investigated the relation between BMI or weight status and any dopamine target in the striatal and midbrain regions of the human brain. A structured literature search was performed and a summary of the extracted findings are presented for each of the four available domains: (1) D2/D3 receptors, (2) dopamine release, (3) dopamine synthesis, and (4) dopamine transporters. Recent proposals of a nonlinear relationship between severity of obesity and dopamine imbalances are described while integrating findings within and across domains, after which limitations of the review are discussed. We conclude that despite many observed associations between obesity and substrates of the dopamine system in humans, it is unlikely that obesity can be traced back to a single dopaminergic cause or consequence. For effective personalized prevention and treatment of obesity, it will be crucial to identify possible dopamine (and non-dopamine) profiles and their functional characteristics.

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