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Age-Related Decrease in Male Extra-Striatal Adenosine A(1) Receptors Measured Using (11)C-MPDX PET

Adenosine A(1) receptors (A(1)Rs) are widely distributed throughout the entire human brain, while adenosine A(2A) receptors (A(2A)Rs) are present in dopamine-rich areas of the brain, such as the basal ganglia. A past study using autoradiography reported a reduced binding ability of A(1)R in the stri...

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Detalles Bibliográficos
Autores principales: Mishina, Masahiro, Kimura, Yuichi, Sakata, Muneyuki, Ishii, Kenji, Oda, Keiichi, Toyohara, Jun, Kimura, Kazumi, Ishiwata, Kiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741655/
https://www.ncbi.nlm.nih.gov/pubmed/29326588
http://dx.doi.org/10.3389/fphar.2017.00903
Descripción
Sumario:Adenosine A(1) receptors (A(1)Rs) are widely distributed throughout the entire human brain, while adenosine A(2A) receptors (A(2A)Rs) are present in dopamine-rich areas of the brain, such as the basal ganglia. A past study using autoradiography reported a reduced binding ability of A(1)R in the striatum of old rats. We developed positron emission tomography (PET) ligands for mapping the adenosine receptors and we successfully visualized the A(1)Rs using 8-dicyclopropylmethyl-1-(11)C-methyl-3-propylxanthine ((11)C-MPDX). We previously reported that the density of A(1)Rs decreased with age in the human striatum, although we could not observe an age-related change in A(2A)Rs. The aim of this study was to investigate the age-related change of the density of A(1)Rs in the thalamus and cerebral cortices of healthy participants using (11)C-MPDX PET. We recruited eight young (22.0 ± 1.7 years) and nine elderly healthy male volunteers (65.7 ± 8.0 years). A dynamic series of decay-corrected PET scans was performed for 60 min starting with the injection of (11)C-MPDX. We placed the circular regions of interest of 10 mm in diameter in (11)C-MPDX PET images. The values for the binding potential (BP(ND)) of (11)C-MPDX in the thalamus, and frontal, temporal, occipital, and parietal cortices were calculated using a graphical analysis, wherein the reference region was the cerebellum. BP(ND) of (11)C-MPDX was significantly lower in elderly participants than young participants in the thalamus, and frontal, temporal, occipital, and parietal cortices. In the human brain, we could observe the age-related decrease in the distribution of A(1)Rs.