Association of cord blood des-acyl ghrelin with birth weight, and placental GHS-R1 receptor expression in SGA, AGA, and LGA newborns

Although ghrelin in cord blood has been associated to birth weight, its role in fetal and postnatal growth has not been elucidated. The aim of this study was to analyze total ghrelin, acyl ghrelin (AG), and des-acyl ghrelin (DAG) in cord blood of newborns with idiopathic birth weight alterations, an...

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Veröffentlicht in:Endocrine 2016-07, Vol.53 (1), p.182-191
Hauptverfasser: González-Domínguez, Martha I., Lazo-de-la-Vega-Monroy, Maria-Luisa, Zaina, Silvio, Sabanero, Myrna, Daza-Benítez, Leonel, Malacara, Juan Manuel, Barbosa-Sabanero, Gloria
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Sprache:eng
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Zusammenfassung:Although ghrelin in cord blood has been associated to birth weight, its role in fetal and postnatal growth has not been elucidated. The aim of this study was to analyze total ghrelin, acyl ghrelin (AG), and des-acyl ghrelin (DAG) in cord blood of newborns with idiopathic birth weight alterations, and to evaluate protein expression of placental GHS-R1, in order to investigate their correlation with birth weight and placental weight. We performed a cross-sectional comparative study in umbilical cord blood and placentas from healthy mothers of SGA, AGA, and LGA (small, adequate and large for gestational age) term newborns ( n  = 20 per group). Cord blood total ghrelin, AG, and DAG were measured by ELISA, and placental GHS-R1 expression was evaluated by Western blot. Cord blood DAG was higher in SGA compared to AGA newborns (902.1 ± 109.1 and 597.4 ± 58.2 pg/ml, respectively, p  = 0.01) while LGA and AGA showed similar values (627.2 ± 76.4 pg/ml for LGA, p  = 0.80). DAG negatively correlated with birthweight ( r  = −0.31, p  = 0.02) and placental weight ( r  = −0.33, p  = 0.02). No differences in AG or total ghrelin were found. GHS-R1 protein in placenta was not differentially expressed among SGA, AGA, and LGA. Our results suggest a role of DAG in intrauterine growth. Further studies are needed in order to elucidate the mechanisms by which DAG participates in fetal growth.
ISSN:1355-008X
1559-0100
DOI:10.1007/s12020-015-0833-1