Hyperglycemia alters retinoic acid catabolism in embryos exposed to a maternal diabetic milieu.
Ontology highlight
ABSTRACT: Pregestational diabetes is highly associated with increased risk of birth defects. We previously reported that the expression of Cyp26a1, the major catabolizing enzyme for controlling retinoic acid (RA) homeostasis, is significantly down-regulated in embryos of diabetic mice, thereby increasing the embryo's susceptibility to malformations caused by RA dysregulation. However, the underlying mechanism for the down-regulation of Cyp26a1 remains unclear. This study aimed to investigate whether elevated maternal blood glucose in the diabetic milieu is a critical factor for the altered Cyp26a1 expression. Streptozotozin-induced diabetic pregnant mice were treated with phlorizin (PHZ) to reduce blood glucose concentrations via induction of renal glucosuria. Embryonic Cyp26a1 expression level, RA
SUBMITTER: Lee LMY
PROVIDER: S-EPMC10449132 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature
ACCESS DATA