Published in:
Open Access
01-10-2016 | Research Article
Strain Differences Determine the Suitability of Animal Models for Noninvasive In Vivo Beta Cell Mass Determination with Radiolabeled Exendin
Authors:
Stefanie M. A. Willekens, Lieke Joosten, Otto C. Boerman, Alexander Balhuizen, Decio L. Eizirik, Martin Gotthardt, Maarten Brom
Published in:
Molecular Imaging and Biology
|
Issue 5/2016
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Abstract
Purpose
Noninvasive beta cell mass (BCM) quantification is a crucial tool to understand diabetes development and progression. [111In]exendin is a promising agent for in vivo beta cell imaging, but tracer testing has been hampered by the lack of well-defined rodent models.
Procedures
Biodistribution and pancreatic uptake of [111In]exendin were compared in rats and mice. In selected models, the amount of [111In]exendin accumulation in the pancreas and other organs was determined using a model of alloxan-induced beta cell loss. GLP-1R expression levels were analyzed by RT-PCR and immunohistochemistry.
Results
Namely Brown Norway rats showed beta-cell-specific tracer accumulation and favorable pancreas-to-background ratios for noninvasive BCM determination. Mice displayed receptor-mediated [111In]exendin uptake in endocrine and exocrine pancreas, in spite of very low GLP-1R expression in exocrine tissue.
Conclusions
Rats display better characteristics for in vivo BCM determination than mice and are suggested as a more adequate model for humans.