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Functional imaging of pharmacological action of SGLT2 inhibitor ipragliflozin via PET imaging using 11 C-MDG.

Authors :
Mitsuoka K
Hayashizaki Y
Murakami Y
Takasu T
Yokono M
Umeda N
Takakura S
Noda A
Miyoshi S
Source :
Pharmacology research & perspectives [Pharmacol Res Perspect] 2016 Jul 01; Vol. 4 (4), pp. e00244. Date of Electronic Publication: 2016 Jul 01 (Print Publication: 2016).
Publication Year :
2016

Abstract

Sodium-dependent glucose cotransporter 2 (SGLT2) is a pharmacological target of type 2 diabetes mellitus. The aim of this study was to noninvasively visualize the pharmacological action of a selective SGLT2 inhibitor ipragliflozin in the kidney using positron emission tomography (PET) imaging with <superscript>11</superscript> C-methyl-d-glucoside ( <superscript>11</superscript> C-MDG), an SGLT-specific radio-labeled substrate. PET imaging with <superscript>11</superscript> C-MDG in vehicle-treated rats demonstrated that intravenously injected <superscript>11</superscript> C-MDG substantially accumulated in the renal cortex, reflecting that the compound was reabsorbed by SGLTs. In contrast, ipragliflozin-treated rats showed significantly lower uptake of <superscript>11</superscript> C-MDG in renal cortex in a dose-related manner, suggesting that ipragliflozin inhibited the renal reabsorption of <superscript>11</superscript> C-MDG. This method of visualizing the mode of action of an SGLT2 inhibitor in vivo has demonstrated the drug's mechanism in reducing renal glucose reabsorption in kidney in living animals.

Details

Language :
English
ISSN :
2052-1707
Volume :
4
Issue :
4
Database :
MEDLINE
Journal :
Pharmacology research & perspectives
Publication Type :
Academic Journal
Accession number :
28116097
Full Text :
https://doi.org/10.1002/prp2.244