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Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period

In mothers who are nursing their infants, increased clearance of plasma metabolites into the mammary gland may reduce ectopic lipid in the liver. No study to date has investigated the role of lactation on liver lipid synthesis in humans, and we hypothesized that lactation would modify fatty acid and...

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Autores principales: Ramos-Roman, Maria A., Syed-Abdul, Majid M., Casey, Brian M., Alger, Jeffry R., Liu, Yu-Lun, Parks, Elizabeth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619182/
https://www.ncbi.nlm.nih.gov/pubmed/36162520
http://dx.doi.org/10.1016/j.jlr.2022.100288
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author Ramos-Roman, Maria A.
Syed-Abdul, Majid M.
Casey, Brian M.
Alger, Jeffry R.
Liu, Yu-Lun
Parks, Elizabeth J.
author_facet Ramos-Roman, Maria A.
Syed-Abdul, Majid M.
Casey, Brian M.
Alger, Jeffry R.
Liu, Yu-Lun
Parks, Elizabeth J.
author_sort Ramos-Roman, Maria A.
collection PubMed
description In mothers who are nursing their infants, increased clearance of plasma metabolites into the mammary gland may reduce ectopic lipid in the liver. No study to date has investigated the role of lactation on liver lipid synthesis in humans, and we hypothesized that lactation would modify fatty acid and glucose handling to support liver metabolism in a manner synchronized with the demands of milk production. Lactating (n = 18) and formula-feeding women (n = 10) underwent metabolic testing at 6-week postpartum to determine whether lactation modified intrahepatic triacylglycerols (IHTGs), measured by proton magnetic resonance spectroscopy. Subjects ingested oral deuterated water to measure fractional de novo lipogenesis (DNL) in VLDL-TG during fasting and during an isotope-labeled clamp at an insulin infusion rate of 10 mU/m(2)/min. Compared with formula-feeding women, we found that lactating women exhibited lower plasma VLDL-TG concentrations, similar IHTG content and similar contribution of DNL to total VLDL-TG production. These findings suggest that lactation lowers plasma VLDL-TG concentrations for reasons that are unrelated to IHTG and DNL. Surprisingly, we determined that the rate of appearance of nonesterified fatty acids was not related to IHTG in either group, and the expected positive association between DNL and IHTG was only significant in formula-feeding women. Further, in lactating women only, the higher the prolactin concentration, the lower the IHTG, while greater DNL strongly associated with elevations in VLDL-TG. In conclusion, we suggest that future studies should investigate the role of lactation and prolactin in liver lipid secretion and metabolism.
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spelling pubmed-96191822022-11-01 Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period Ramos-Roman, Maria A. Syed-Abdul, Majid M. Casey, Brian M. Alger, Jeffry R. Liu, Yu-Lun Parks, Elizabeth J. J Lipid Res Research Article In mothers who are nursing their infants, increased clearance of plasma metabolites into the mammary gland may reduce ectopic lipid in the liver. No study to date has investigated the role of lactation on liver lipid synthesis in humans, and we hypothesized that lactation would modify fatty acid and glucose handling to support liver metabolism in a manner synchronized with the demands of milk production. Lactating (n = 18) and formula-feeding women (n = 10) underwent metabolic testing at 6-week postpartum to determine whether lactation modified intrahepatic triacylglycerols (IHTGs), measured by proton magnetic resonance spectroscopy. Subjects ingested oral deuterated water to measure fractional de novo lipogenesis (DNL) in VLDL-TG during fasting and during an isotope-labeled clamp at an insulin infusion rate of 10 mU/m(2)/min. Compared with formula-feeding women, we found that lactating women exhibited lower plasma VLDL-TG concentrations, similar IHTG content and similar contribution of DNL to total VLDL-TG production. These findings suggest that lactation lowers plasma VLDL-TG concentrations for reasons that are unrelated to IHTG and DNL. Surprisingly, we determined that the rate of appearance of nonesterified fatty acids was not related to IHTG in either group, and the expected positive association between DNL and IHTG was only significant in formula-feeding women. Further, in lactating women only, the higher the prolactin concentration, the lower the IHTG, while greater DNL strongly associated with elevations in VLDL-TG. In conclusion, we suggest that future studies should investigate the role of lactation and prolactin in liver lipid secretion and metabolism. American Society for Biochemistry and Molecular Biology 2022-09-23 /pmc/articles/PMC9619182/ /pubmed/36162520 http://dx.doi.org/10.1016/j.jlr.2022.100288 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Ramos-Roman, Maria A.
Syed-Abdul, Majid M.
Casey, Brian M.
Alger, Jeffry R.
Liu, Yu-Lun
Parks, Elizabeth J.
Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title_full Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title_fullStr Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title_full_unstemmed Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title_short Lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
title_sort lactation alters the relationship between liver lipid synthesis and hepatic fat stores in the postpartum period
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619182/
https://www.ncbi.nlm.nih.gov/pubmed/36162520
http://dx.doi.org/10.1016/j.jlr.2022.100288
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