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Decreased placental folate transporter expression and activity in first and second trimester in obese mothers
Institution:1. Grup Recerca Infància i Entorn (GRIE), Institut Hospital del Mar d''Investigacions Mèdiques (IMIM), Barcelona, Spain;2. Red de Salud Materno-Infantil y del Desarrollo (SAMID), Programa RETICS, Instituto Carlos III, Madrid, Spain;3. Departament Pediatria, Obstetricia i Ginecologia i Medicina Preventiva, Universitat Autònoma Barcelona (UAB), Bellaterra, Spain;4. Servei Pediatria, Parc de Salut Mar, Barcelona, Spain;1. Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of South Alabama School of Medicine, Mobile, AL, USA;2. Magee-Womens Research Institute, Pittsburgh, PA, USA;1. Laboratorio de Nutrición y Regulación Metabólica, Unidad de Nutrición Humana, Instituto de Nutrición y Tecnología de los Alimentos (INTA), Universidad de Chile, Chile;2. Instituto de Investigaciones Materno-Infantil (IDIMI), División Ciencias Médicas Centro, Facultad de Medicina, Universidad de Chile, Chile;1. Mercy Perinatal Research Centre, Mercy Hospital for Women, Heidelberg, Victoria, Australia;2. Obstetrics, Nutrition and Endocrinology Group, Department of Obstetrics and Gynaecology, University of Melbourne, Victoria, Australia
Abstract:Obese women have an approximately twofold higher risk to deliver an infant with neural tube defects (NTDs) despite folate supplementation. Placental transfer of folate is mediated by folate receptor alpha (FR-α), proton coupled folate transporter (PCFT), and reduced folate carrier (RFC). Decreased placental transport may contribute to NTDs in obese women. Serum folate levels were measured and placental tissue was collected from 13 women with normal BMI (21.9±1.9) and 11 obese women (BMI 33.1±2.8) undergoing elective termination at 8–22 weeks of gestation. The syncytiotrophoblast microvillous plasma membranes (MVM) were isolated using homogenization, magnesium precipitation, and differential centrifugation. MVM expression of FR-α, PCFT and RFC was determined by western blot. Folate transport capacity was assessed using radiolabeled methyl-tetrahydrofolate and rapid filtration techniques. Differences in expression and transport capacity were adjusted for gestational age and maternal age in multivariable regression models. P<.05 was considered statistically significant. Serum folate levels were not significantly different between groups. Placental MVM folate transporter expression did not change with gestational age. MVM RFC (?19%) and FR-α (?17%) expression was significantly reduced in placentas from obese women (P<.05). MVM folate transporter activity was reduced by?52% (P<.05) in obese women. These differences remained after adjustment for gestational age. There was no difference in mTOR signaling between groups. In conclusion, RFC and FR alpha expression and transporter activity in the placental MVM are significantly reduced in obese women in early pregnancy. These results may explain the higher incidence of NTDs in infants of obese women with adequate serum folate.
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