In vivo imaging of dopamine D1 receptor and activated microglia in attention-deficit/hyperactivity disorder: a positron emission tomography study

Alterations in the cortical dopamine system and microglial activation have been implicated in the pathophysiology of attention-deficit/hyperactivity disorder (ADHD), one of neurodevelopmental disorders that can be conventionally treated with a dopamine enhancer (methylphenidate) albeit unsatisfactor...

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Bibliographic Details
Published in:Molecular psychiatry 2021-09, Vol.26 (9), p.4958-4967
Main Authors: Yokokura, Masamichi, Takebasashi, Kiyokazu, Takao, Akiyo, Nakaizumi, Kyoko, Yoshikawa, Etsuji, Futatsubashi, Masami, Suzuki, Katsuaki, Nakamura, Kazuhiko, Yamasue, Hidenori, Ouchi, Yasuomi
Format: Article
Language:English
Subjects:
Attention Deficit Disorder with Hyperactivity - diagnostic imaging
Attention deficit hyperactivity disorder
Cognitive ability
Cortex (cingulate)
Diagnosis
Dopamine
Dopamine D1 receptors
Dopamine receptors
Dorsolateral Prefrontal Cortex
Health aspects
Humans
Hyperactivity
Magnetic Resonance Imaging
Methylphenidate
Microglia
Neurodevelopmental disorders
Neuroimaging
PET imaging
Physiological aspects
Positron emission tomography
Prefrontal Cortex
Processing speed
Receptors, Dopamine D1
Therapeutic targets
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Summary:Alterations in the cortical dopamine system and microglial activation have been implicated in the pathophysiology of attention-deficit/hyperactivity disorder (ADHD), one of neurodevelopmental disorders that can be conventionally treated with a dopamine enhancer (methylphenidate) albeit unsatisfactorily. Here, we investigated the contributions of the dopamine D1 receptor (D1R) and activated microglia and their interactions to the clinical severities in ADHD individuals using positron emission tomography (PET). Twenty-four psychotropic-naïve ADHD individuals and 24 age- and sex-matched typically developing (TD) subjects underwent PET measurements with [ C]SCH23390 for the D1R and [ C](R)PK11195 for activated microglia as well as assessments of clinical symptoms and cognitive functions. The ADHD individuals showed decreased D1R in the anterior cingulate cortex (ACC) and increased activated microglia in the dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex (OFC) compared with the TD subjects. The decreased D1R in the ACC was associated with severe hyperactivity in the participants with ADHD. Microglial activation in the DLPFC were associated with deficits in processing speed and attentional ability, and that in the OFC was correlated with lower processing speed in the ADHD individuals. Furthermore, positive correlations between the D1R and activated microglia in both the DLPFC and the OFC were found to be significantly specific to the ADHD group and not to the TD group. The current findings suggest that microglial activation and the D1R reduction as well as their aberrant interactions underpin the neurophysiological mechanism of ADHD and indicate these biomolecular changes as a novel therapeutic target.
ISSN:1359-4184
1476-5578
DOI:10.1038/s41380-020-0784-7