Development of a New Radiofluorinated Quinoline Analog for PET Imaging of Phosphodiesterase 5 (PDE5) in Brain

Phosphodiesterases (PDEs) are enzymes that play a major role in cell signalling by hydrolysing the secondary messengers cyclic adenosine monophosphate (cAMP) and/or cyclic guanosine monophosphate (cGMP) throughout the body and brain. Altered cyclic nucleotide-mediated signalling has been associated...

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Main Authors: Jianrong Liu (Author), Barbara Wenzel (Author), Sladjana Dukic-Stefanovic (Author), Rodrigo Teodoro (Author), Friedrich-Alexander Ludwig (Author), Winnie Deuther-Conrad (Author), Susann Schröder (Author), Jean-Michel Chezal (Author), Emmanuel Moreau (Author), Peter Brust (Author), Aurélie Maisonial-Besset (Author)
Format: Book
Published: MDPI AG, 2016-04-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Jianrong Liu  |e author 
700 1 0 |a Barbara Wenzel  |e author 
700 1 0 |a Sladjana Dukic-Stefanovic  |e author 
700 1 0 |a Rodrigo Teodoro  |e author 
700 1 0 |a Friedrich-Alexander Ludwig  |e author 
700 1 0 |a Winnie Deuther-Conrad  |e author 
700 1 0 |a Susann Schröder  |e author 
700 1 0 |a Jean-Michel Chezal  |e author 
700 1 0 |a Emmanuel Moreau  |e author 
700 1 0 |a Peter Brust  |e author 
700 1 0 |a Aurélie Maisonial-Besset  |e author 
245 0 0 |a Development of a New Radiofluorinated Quinoline Analog for PET Imaging of Phosphodiesterase 5 (PDE5) in Brain 
260 |b MDPI AG,   |c 2016-04-01T00:00:00Z. 
500 |a 1424-8247 
500 |a 10.3390/ph9020022 
520 |a Phosphodiesterases (PDEs) are enzymes that play a major role in cell signalling by hydrolysing the secondary messengers cyclic adenosine monophosphate (cAMP) and/or cyclic guanosine monophosphate (cGMP) throughout the body and brain. Altered cyclic nucleotide-mediated signalling has been associated with a wide array of disorders, including neurodegenerative disorders. Recently, PDE5 has been shown to be involved in neurodegenerative disorders such as Alzheimer's disease, but its precise role has not been elucidated yet. To visualize and quantify the expression of this enzyme in brain, we developed a radiotracer for specific PET imaging of PDE5. A quinoline-based lead compound has been structurally modified resulting in the fluoroethoxymethyl derivative ICF24027 with high inhibitory activity towards PDE5 (IC50 = 1.86 nM). Radiolabelling with fluorine-18 was performed by a one-step nucleophilic substitution reaction using a tosylate precursor (RCY(EOB) = 12.9% ± 1.8%; RCP > 99%; SA(EOS) = 70-126 GBq/μmol). In vitro autoradiographic studies of [18F]ICF24027 on different mouse tissue as well as on porcine brain slices demonstrated a moderate specific binding to PDE5. In vivo studies in mice revealed that [18F]ICF24027 was metabolized under formation of brain penetrable radiometabolites making the radiotracer unsuitable for PET imaging of PDE5 in brain. 
546 |a EN 
690 |a PDE5 
690 |a PET imaging 
690 |a fluorine-18 
690 |a quinoline 
690 |a micellar chromatography 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 9, Iss 2, p 22 (2016) 
787 0 |n http://www.mdpi.com/1424-8247/9/2/22 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/ee4229335f3542d7a23f1b8d68bef7d3  |z Connect to this object online.