Gestational Diabetes Mellitus and Small-for-Gestational-Age: An Insight into the Placental Molecular Biomarkers.
Christian GiommiMarta LombόNina MontikMichela PaolucciValentina NotarstefanoGiovanni Delli CarpiniAndrea CiavattiniAntonio RagusaFrancesca MaradonnaElisabetta GiorginiOliana CarnevaliPublished in: International journal of molecular sciences (2023)
Gestational diabetes mellitus (GDM) and small-for-gestational-age (SGA) are two metabolic-related diseases that could affect women during pregnancy. Considering that the chorionic villi (CVs) are crucial structures for the feto-maternal exchange, the alterations in their conformation have been linked to an imbalanced metabolic environment of placenta. In this study, a multidisciplinary approach has been carried out to describe the changes occurring in the placental CVs of GDM and SGA patients. The results revealed higher levels of superoxide dismutase 1 (SOD-1) and catalase (CAT), especially in the GDM placentae, which could be correlated with the hyperglycemic environment characteristic of this pathology. Furthermore, spectroscopy and histologic analyses revealed that both pathologies modify the placental lipid composition altering its structure. However, SGA induces lipid peroxidation and reduces collagen deposition within the CVs. Since the endocannabinoid system (ECS) is involved in placentation and different metabolic activities, the cannabinoid receptor 1 (CB1) and transient receptor potential cation channel subfamily V member 1 (TRPV-1) were analyzed. No changes have been observed either at general or specific levels in the CVs comparing control and pathological samples, suggesting the non-involvement of the cannabinoid system in these two pathologies.
Keyphrases
- gestational age
- birth weight
- pregnancy outcomes
- preterm birth
- pregnant women
- weight gain
- end stage renal disease
- newly diagnosed
- high resolution
- ejection fraction
- single cell
- chronic kidney disease
- single molecule
- polycystic ovary syndrome
- prognostic factors
- hydrogen peroxide
- metabolic syndrome
- brain injury
- weight loss
- binding protein
- transcription factor
- solid state
- amyotrophic lateral sclerosis
- human health
- mass spectrometry
- drug induced
- skeletal muscle