TY - JOUR
T1 - Docosahexaenoic acid supplementation in pregnancy modulates placental cellular signaling and nutrient transport capacity in obese women
AU - Lager, Susanne
AU - Ramirez, Vanessa I.
AU - Acosta, Ometeotl
AU - Meireles, Christiane
AU - Miller, Evelyn
AU - Gaccioli, Francesca
AU - Rosario, Fredrick J.
AU - Gelfond, Jonathan A.L.
AU - Hakala, Kevin
AU - Weintraub, Susan T.
AU - Krummel, Debra A.
AU - Powell, Theresa L.
N1 - Funding Information:
Financial Support: This study was supported by grants from National Institutes of Health R21HL093532 (to D.A.K. and T.L.P), 8UL1TR000149, UL1 TR001120, and the Mike Hogg Fund (to T.L.P.), the Swedish Research Council (to S.L.), and the Swedish Society of Endocrinology (to S.L.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
PY - 2017
Y1 - 2017
N2 - Context: Maternal obesity in pregnancy has profound impacts on maternal metabolism and promotes placental nutrient transport, which may contribute to fetal overgrowth in these pregnancies. The fatty acid docosahexaenoic acid (DHA) has bioactive properties that may improve outcomes in obese pregnant women by modulating placental function. Objective: To determine the effects of DHA supplementation in obese pregnant women on maternal metabolism and placental function. Design: Pregnant women were supplemented with DHA or placebo. Maternal fasting blood was collected at 26 and 36 weeks' gestation, and placentas were collected at term. Setting: Academic health care institution. Subjects: Thirty-eight pregnant women with pregravid body mass index $30 kg/m2. Intervention: DHA (800 mg, algal oil) or placebo (corn/soy oil) daily from 26 weeks to term. Main Outcomes: DHA content of maternal erythrocyte and placental membranes, maternal fasting blood glucose, cytokines, metabolic hormones, and circulating lipidswere determined. Insulin,mTOR, and inflammatory signaling were assessed in placental homogenates, and nutrient transport capacity was determined in isolated syncytiotrophoblast plasma membranes. Results: DHA supplementation increased erythrocyte (P , 0.0001) and placental membrane DHA levels (P , 0.0001) but did not influence maternal inflammatory status, insulin sensitivity, or lipids. DHA supplementation decreased placental inflammation, amino acid transporter expression, and activity (P , 0.01) and increased placental protein expression of fatty acid transporting protein 4 (P , 0.05). Conclusions: Maternal DHA supplementation in pregnancy decreases placental inflammation and differentially modulates placental nutrient transport capacity and may mitigate adverse effects of maternal obesity on placental function.
AB - Context: Maternal obesity in pregnancy has profound impacts on maternal metabolism and promotes placental nutrient transport, which may contribute to fetal overgrowth in these pregnancies. The fatty acid docosahexaenoic acid (DHA) has bioactive properties that may improve outcomes in obese pregnant women by modulating placental function. Objective: To determine the effects of DHA supplementation in obese pregnant women on maternal metabolism and placental function. Design: Pregnant women were supplemented with DHA or placebo. Maternal fasting blood was collected at 26 and 36 weeks' gestation, and placentas were collected at term. Setting: Academic health care institution. Subjects: Thirty-eight pregnant women with pregravid body mass index $30 kg/m2. Intervention: DHA (800 mg, algal oil) or placebo (corn/soy oil) daily from 26 weeks to term. Main Outcomes: DHA content of maternal erythrocyte and placental membranes, maternal fasting blood glucose, cytokines, metabolic hormones, and circulating lipidswere determined. Insulin,mTOR, and inflammatory signaling were assessed in placental homogenates, and nutrient transport capacity was determined in isolated syncytiotrophoblast plasma membranes. Results: DHA supplementation increased erythrocyte (P , 0.0001) and placental membrane DHA levels (P , 0.0001) but did not influence maternal inflammatory status, insulin sensitivity, or lipids. DHA supplementation decreased placental inflammation, amino acid transporter expression, and activity (P , 0.01) and increased placental protein expression of fatty acid transporting protein 4 (P , 0.05). Conclusions: Maternal DHA supplementation in pregnancy decreases placental inflammation and differentially modulates placental nutrient transport capacity and may mitigate adverse effects of maternal obesity on placental function.
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U2 - 10.1210/jc.2017-01384
DO - 10.1210/jc.2017-01384
M3 - Article
C2 - 29053802
AN - SCOPUS:85039863393
VL - 102
SP - 4557
EP - 4567
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
SN - 0021-972X
IS - 12
ER -