Maternal Metformin Treatment Improves Developmental and Metabolic Traits of IUGR Fetuses.
Consolación Garcia-ContrerasMarta Vázquez-GómezJosé Luis Pesantez-PachecoLaura Torres-RoviraAna Heras-MolinaTeresa EncinasSusana AstizAntonio González-BulnesPublished in: Biomolecules (2019)
Metformin is an anti-hyperglycemic drug widely used for the treatment of insulin resistance and glucose intolerance and is currently considered for preventing large-for-gestational-age (LGA) offspring in pregnant women affected by obesity or diabetes. Our hypothesis was the opposite-metformin may be used for improving the development of offspring affected by intrauterine growth restriction (IUGR) and preventing the appearance of small-for-gestational-age (SGA) neonates in non-obese and non-diabetic but malnourished pregnancies. The current study, performed in a swine preclinical model of IUGR by undernutrition, showed that fetuses in the treated group showed no significant increases in body-weight, but showed a significantly higher weight of the brain, the total thoracic and abdominal viscera, the liver, the kidneys, the spleen, and the adrenal glands. Maternal metformin treatment was also related to significant increases in the fetal plasma concentration of parameters indicative of glycemic (glucose and fructosamine) and lipid profiles (triglycerides). Overall, these results suggest a protective effect of the treatment on the developmental competence of the fetuses. These findings may be of high value for human medicine in case of maternal malnutrition, since metformin is a cheap drug easily available, but also in case of placental deficiency, since metformin seems to improve placental development and function.
Keyphrases
- gestational age
- birth weight
- type diabetes
- insulin resistance
- pregnant women
- preterm birth
- body weight
- adipose tissue
- metabolic syndrome
- high fat diet
- weight loss
- emergency department
- combination therapy
- body mass index
- spinal cord
- multiple sclerosis
- gene expression
- dna methylation
- spinal cord injury
- mesenchymal stem cells
- blood pressure
- blood glucose
- blood brain barrier
- glycemic control