Gestational Diabetes Mellitus and Small-for-Gestational-Age: An Insight into the Placental Molecular Biomarkers

被引:4
作者
Giommi, Christian [1 ,2 ]
Lombo, Marta [1 ,2 ,3 ]
Montik, Nina [4 ]
Paolucci, Michela [4 ]
Notarstefano, Valentina [1 ]
Delli Carpini, Giovanni [4 ]
Ciavattini, Andrea [4 ]
Ragusa, Antonio [5 ]
Maradonna, Francesca [1 ,2 ]
Giorgini, Elisabetta [1 ]
Carnevali, Oliana [1 ,2 ]
机构
[1] Univ Politecn Marche, Dept Life & Environm Sci, I-60131 Ancona, Italy
[2] INBB Consorzio Interuniv Biosistemi & Biostrutture, I-00136 Rome, Italy
[3] Univ Leon, Fac Biol & Environm Sci, Dept Mol Biol, Leon 24071, Spain
[4] Univ Politecn Marche, Dept Odontostomatol & Specialized Clin Sci, I-60020 Ancona, Italy
[5] Univ Campus Bio Med Roma, Dept Obstet & Gynecol, I-00128 Rome, Italy
关键词
FTIRI; placenta; GDM; SGA; endocannabinoid receptors; OXIDATIVE STRESS; GROWTH; HYPERGLYCEMIA; PERMEABILITY; SPECTROSCOPY; EXPRESSION; PREGNANCY; PLASMA; ACID;
D O I
10.3390/ijms24032240
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页数:16
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