Direct Monitoring of γ-Glutamyl Transpeptidase Activity In Vivo Using a Hyperpolarized (13) C-Labeled Molecular Probe.

Détails

ID Serval
serval:BIB_43E53D072042
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Direct Monitoring of γ-Glutamyl Transpeptidase Activity In Vivo Using a Hyperpolarized (13) C-Labeled Molecular Probe.
Périodique
Angewandte Chemie
Auteur⸱e⸱s
Nishihara T., Yoshihara H.A., Nonaka H., Takakusagi Y., Hyodo F., Ichikawa K., Can E., Bastiaansen J.A., Takado Y., Comment A., Sando S.
ISSN
1521-3773 (Electronic)
ISSN-L
1433-7851
Statut éditorial
Publié
Date de publication
26/08/2016
Peer-reviewed
Oui
Volume
55
Numéro
36
Pages
10626-10629
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
The γ-glutamyl transpeptidase (GGT) enzyme plays a central role in glutathione homeostasis. Direct detection of GGT activity could provide critical information for the diagnosis of several pathologies. We propose a new molecular probe, γ-Glu-[1-(13) C]Gly, for monitoring GGT activity in vivo by hyperpolarized (HP) (13) C magnetic resonance (MR). The properties of γ-Glu-[1-(13) C]Gly are suitable for in vivo HP (13) C metabolic analysis since the chemical shift between γ-Glu-[1-(13) C]Gly and its metabolic product, [1-(13) C]Gly, is large (4.3 ppm) and the T1 of both compounds is relatively long (30 s and 45 s, respectively, in H2 O at 9.4 T). We also demonstrate that γ-Glu-[1-(13) C]Gly is highly sensitive to in vivo modulation of GGT activity induced by the inhibitor acivicin.
Mots-clé
Animals, Enzyme Assays/methods, Enzyme Inhibitors/pharmacology, Glutathione/metabolism, Isoxazoles/pharmacology, Molecular Probes/metabolism, Nuclear Magnetic Resonance, Biomolecular/methods, Rats, gamma-Glutamyltransferase/antagonists & inhibitors, gamma-Glutamyltransferase/metabolism, NMR spectroscopy, biosensors, dynamic nuclear polarization, hyperpolarization, γ-glutamyl transpeptidase
Pubmed
Web of science
Open Access
Oui
Création de la notice
11/01/2018 10:29
Dernière modification de la notice
20/08/2019 14:48
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