Proinflammation in maternal and fetal livers and circulating miR-122 dysregulation in a GDM rat model induced by intrauterine programming

FORNES, DAIANA; WHITE, VERÓNICA; FORNES, DAIANA; WHITE, VERÓNICA; ROBERTI, SABRINA LORENA; JAWERBAUM, ALICIA; ROBERTI, SABRINA LORENA; JAWERBAUM, ALICIA; HEINECKE, FLORENCIA; CAPOBIANCO, EVANGELINA; HEINECKE, FLORENCIA; CAPOBIANCO, EVANGELINA

MOLECULAR AND CELLULAR ENDOCRINOLOGY.

ELSEVIER IRELAND LTD

Año: 2020 vol. 510

0303-7207

In gestational diabetes mellitus (GDM) pregnancies, a compromised fetal liver may impact offspring´s metabolic health. Here, we aimed to address prooxidant, proinflammatory and profibrotic markers in the livers from GDM rats and their fetuses, and to analyze the expression of miR-122 (a relevant microRNA in liver pathophysiology) in fetal and maternal plasma of GDM rats, as well as in the fetal livers of neonatal streptozotocin-induced (nSTZ) diabetic rats, the rats that generate GDM through intrauterine programming. GDM and nSTZ rats were evaluated on day 21 of pregnancy. We found increased nitric oxide production and lipoperoxidation in the livers from GDM rats and their fetuses compared to controls. Livers from GDM fetuses also showed increased levels of connective tissue growth factor and matrix metalloproteinase-2. The expression of miRNA-122 was downregulated in the plasma from GDM rats and their male fetuses, as well as in the livers from male fetuses of nSTZ diabetic rats. miR-122 levels were regulated both in vitro through PPARγ activation and in vivo through a maternal diet enriched in PPAR ligands. Our findings revealed a prooxidant/proinflammatory environment in the livers from GDM rats and their fetuses and a dysregulation of miR-122, likely relevant in the programming of offspring´s diseases.