Author/Authors :
Dahl Overgaard, Maria Aarhus University Hospital - Aarhus, Denmark , Søndergaard Duvald, Christina Aarhus University Hospital - Aarhus, Denmark , Holm Vendelbo, Mikkel Department of Nuclear Medicine and PET Centre - Aarhus University Hospital - Aarhus, Denmark , Bønløkke Pedersen, Steen Aarhus University Hospital - Aarhus, Denmark , Jakobsen, Steen Department of Nuclear Medicine and PET Centre - Aarhus University Hospital - Aarhus, Denmark , Kristian Olsen Alstrup, Aage Department of Nuclear Medicine and PET Centre - Aarhus University Hospital - Aarhus, Denmark , Mikkelsen, Emmeli Aarhus University Hospital - Aarhus, Denmark , Glud Ovesen, Per Department of Obstetrics and Gynecology - Aarhus University Hospital - Aarhus, Denmark , Pedersen, Michael Aarhus University Hospital - Aarhus, Denmark
Abstract :
While metformin is the first-line pharmacological treatment of diabetes mellitus type 2, this drug is not considered
safe to use in pregnant women because of its unknown consequences for the fetus. In this study, we aimed to investigate the
biodistribution of metformin in the pregnant chinchilla, a species exhibiting placental characteristics comparable with the
pregnant woman. Furthermore, we aimed to investigate the expression of metformin transporters in humans and chinchillas,
respectively, in order to evaluate the pregnant chinchilla as a novel animal model for the use of metformin in pregnancy. Methods.
Three chinchillas in the last part of gestation were injected with [11C]-metformin and scanned by PET/CT for 70 minutes to
visualize the distribution. To investigate the difference in expression of placenta transporters between humans and chinchillas,
PCR was performed on samples from five chinchilla placentae and seven human placentae. Results. Dynamic PET with [11C]-
metformin showed that the metformin distribution in chinchillas was similar to that in nonpregnant humans, with signal from
kidneys, liver, bladder, and submandibular glands. Conversely, no radioactive signal was observed from the fetuses, and no
metformin was accumulated in the chinchilla fetus when measuring the SUV. PCR of placental mRNA showed that the human
placentae expressed OCT3, whereas the chinchilla placentae expressed OCT1. Conclusion. Since metformin did not pass the
placenta barrier in the pregnant chinchilla, as it is known to do in humans, we do not suggest the chinchilla as a future animal
model of metformin in pregnancies.
Keywords :
Biodistribution , mRNA , Transporters , GDM