| Literature DB >> 32176867 |
Harleen Kaur1, Beverly S Muhlhausler2, Pamela S-L Sim3, Amanda Page4, Hui Li5, Maria Nunez-Salces6, Georgia S Clarke7, Lili Huang8, Rebecca L Wilson9, Johannes D Veldhuis10, Chen Chen11, Claire Trelford Roberts12, Kathryn L Gatford13.
Abstract
Circulating growth hormone (GH) concentrations increase during pregnancy in mice and remain pituitary-derived. Whether abundance or activation of the GH secretagogue, ghrelin increase during pregnancy or in response to dietary octanoic acid supplementation are unclear. We therefore measured circulating GH profiles in late pregnant C57BL/6J mice and in aged-matched non-pregnant females, fed standard laboratory chow supplemented with 5% octanoic or palmitic (control) acid (n=4-13/group). Serum total and acyl-ghrelin concentrations, stomach and placenta ghrelin mRNA and protein expression, Pcsk1 (encoding prohormone convertase 1/3) and Mboat4 (membrane bound O-acyl transferase 4) mRNA were determined at zeitgeber (ZT) 13 and ZT23. Total and basal GH secretion were higher in late pregnant than non-pregnant mice (P<0.001), regardless of diet. At ZT13, serum concentrations of total (P=0.004), but not acyl-ghrelin, and the density of ghrelin-positive cells in the gastric antrum (P=0.019) were higher, and gastric Mboat4 and Pcsk1 mRNA expression were lower in pregnant than non-pregnant mice at ZT23. In the placenta, ghrelin protein was localised mostly to labyrinthine trophoblast cells. Serum acyl-, but not total, ghrelin was lower at mid-pregnancy than in non-pregnant mice, but not different at early or late pregnancy. In conclusion, dietary supplementation with 5% octanoic acid did not increase activation of ghrelin in female mice. Our results further suggest that increases in maternal GH secretion throughout murine pregnancy are not due to circulating acyl-ghrelin acting at the pituitary. Nevertheless, time-dependent increased circulating total ghrelin could potentially increase ghrelin action in tissues that express the acylating enzyme and receptor.Entities:
Year: 2020 PMID: 32176867 DOI: 10.1530/JOE-20-0072
Source DB: PubMed Journal: J Endocrinol ISSN: 0022-0795 Impact factor: 4.286