Accumulation of advanced glycation end products in the rabbit blastocyst under maternal diabetes.

Abstract

Diabetes mellitus (DM) during pregnancy is one of the leading causes of perinatal morbidity and birth defects. The mechanism by which maternal hyperglycemia, the major teratogenic factor, induces embryonic malformations remains unclear. Advanced glycation end products (AGEs) are known to accumulate during the course of DM and contribute to the development of diabetic complications. Employing a diabetic rabbit model, we investigated the influence of maternal hyperglycemia during the preimplantation period on AGE formation (pentosidine, argpyrimidine, and N(ϵ)-carboxymethyllysine (CML)) in the reproductive tract and the embryo itself. As a consequence of type 1 DM, the AGE levels in blood plasma increased up to 50%, correlating closely with an AGE accumulation in the endometrium of diabetic females. Embryos from diabetic mothers had increased protein-bound CML levels and showed enhanced fluorescent signals for AGE-specific fluorescence in the blastocyst cavity fluid (BCF). The quantification of CML by HPLC-mass spectrometry (MS/MS) showed a higher amount of soluble CML in the BCF of blastocysts from diabetic rabbits (0.26±0.05 μmol/l) compared with controls (0.18±0.02 μmol/l). The high amount of AGEs in blastocysts from diabetic mothers correlates positively with an increased AGER (receptor for AGE (RAGE)) mRNA expression. Our study gives alarming insights into the consequences of poorly controlled maternal diabetes for AGE formation in the embryo. Maternal hyperglycemia during the preimplantation period is correlated with an increase in AGE formation in the uterine environment and the embryo itself. This may influence the development of the embryo through increased AGE-mediated cellular stress by RAGEs.

• Authors: Elisa Haucke, Alexander Navarrete Santos, Andreas Simm, Christian Henning, Marcus A Glomb, Jacqueline Gürke, Maria Schindler, Bernd Fischer, Anne Navarrete Santos
• Journal: Reproduction (Cambridge, England) (Reproduction) Vol. 148 Issue 2 Pg. 169-78 (Aug 2014) ISSN: 1741-7899 [Electronic] England
• PMID: 24821834 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2014 Society for Reproduction and Fertility.

Chemical References

• Glycation End Products, Advanced
• RNA, Messenger
• Receptor for Advanced Glycation End Products
• Receptors, Immunologic

Topics

• Animals
• Blastocyst (metabolism, pathology)
• Cells, Cultured
• Chromatography, High Pressure Liquid
• Diabetes Mellitus, Experimental (etiology, metabolism, pathology)
• Diabetes Mellitus, Type 1 (etiology, metabolism, pathology)
• Diabetes, Gestational (metabolism, pathology)
• Female
• Glycation End Products, Advanced (genetics, metabolism)
• Hyperglycemia (complications, physiopathology)
• Immunoenzyme Techniques
• Male
• Pregnancy
• RNA, Messenger (genetics)
• Rabbits
• Real-Time Polymerase Chain Reaction
• Receptor for Advanced Glycation End Products
• Receptors, Immunologic (genetics, metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• Tandem Mass Spectrometry