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Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring

Maternal obesity and/or high‐fat diet during pregnancy predispose the offspring to metabolic disease. It is however unclear how pre‐natal and post‐natal exposure respectively affect the risk of hepatic steatosis and the trajectory towards non‐alcoholic steatohepatitis in the offspring. We investigat...

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Autores principales: Ingvorsen, Camilla, Lelliott, Christopher J., Brix, Susanne, Hellgren, Lars I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818417/
https://www.ncbi.nlm.nih.gov/pubmed/32772427
http://dx.doi.org/10.1111/1440-1681.13396
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author Ingvorsen, Camilla
Lelliott, Christopher J.
Brix, Susanne
Hellgren, Lars I.
author_facet Ingvorsen, Camilla
Lelliott, Christopher J.
Brix, Susanne
Hellgren, Lars I.
author_sort Ingvorsen, Camilla
collection PubMed
description Maternal obesity and/or high‐fat diet during pregnancy predispose the offspring to metabolic disease. It is however unclear how pre‐natal and post‐natal exposure respectively affect the risk of hepatic steatosis and the trajectory towards non‐alcoholic steatohepatitis in the offspring. We investigate hepatic lipid metabolism and how these factors are related to metabolic outcome in new born and young rats. Rat dams were exposed to a high‐fat/high sucrose (HFHS) diet for 17 weeks prior to mating and during pregnancy. After birth, female offspring were killed and male offspring were cross‐fostered, creating four groups; Control‐born pups lactated by control (CC) or HFHS dams (CH) and HFHS‐born pups lactated by control (HC) or HFHS dams (HH). At 4 weeks of age, pups were killed and metabolic markers in plasma were assayed, together with hepatic lipid composition and expression of relevant genes. Female HFHS neonates had smaller livers at birth (P < .05), a reduced hepatic lipid content (P < .05) and altered lipid composition. The post‐natal environment dominated the metabolic profile in the male offspring at 4 weeks of age. Offspring exposed to a HFHS environment post‐natally had increased adiposity (P < .0001), increased hepatic triacylglycrol accumulation (P < .0001), and an altered lipid profile with elevated n‐6 polyunsaturated fatty acid (PUFA) levels (P < .0001) and a reduction in ceramide (P < .001) and monounsaturated fatty acid (MUFA) (P < .0001). In summary, maternal HFHS diet during gestation affects the hepatic lipid profile in neonates. The pre‐natal exposure becomes less pronounced in young male offspring at 4 weeks of age, where the post‐natal diet has the largest impact.
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spelling pubmed-78184172021-01-29 Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring Ingvorsen, Camilla Lelliott, Christopher J. Brix, Susanne Hellgren, Lars I. Clin Exp Pharmacol Physiol Original Articles Maternal obesity and/or high‐fat diet during pregnancy predispose the offspring to metabolic disease. It is however unclear how pre‐natal and post‐natal exposure respectively affect the risk of hepatic steatosis and the trajectory towards non‐alcoholic steatohepatitis in the offspring. We investigate hepatic lipid metabolism and how these factors are related to metabolic outcome in new born and young rats. Rat dams were exposed to a high‐fat/high sucrose (HFHS) diet for 17 weeks prior to mating and during pregnancy. After birth, female offspring were killed and male offspring were cross‐fostered, creating four groups; Control‐born pups lactated by control (CC) or HFHS dams (CH) and HFHS‐born pups lactated by control (HC) or HFHS dams (HH). At 4 weeks of age, pups were killed and metabolic markers in plasma were assayed, together with hepatic lipid composition and expression of relevant genes. Female HFHS neonates had smaller livers at birth (P < .05), a reduced hepatic lipid content (P < .05) and altered lipid composition. The post‐natal environment dominated the metabolic profile in the male offspring at 4 weeks of age. Offspring exposed to a HFHS environment post‐natally had increased adiposity (P < .0001), increased hepatic triacylglycrol accumulation (P < .0001), and an altered lipid profile with elevated n‐6 polyunsaturated fatty acid (PUFA) levels (P < .0001) and a reduction in ceramide (P < .001) and monounsaturated fatty acid (MUFA) (P < .0001). In summary, maternal HFHS diet during gestation affects the hepatic lipid profile in neonates. The pre‐natal exposure becomes less pronounced in young male offspring at 4 weeks of age, where the post‐natal diet has the largest impact. John Wiley and Sons Inc. 2020-09-07 2021-01 /pmc/articles/PMC7818417/ /pubmed/32772427 http://dx.doi.org/10.1111/1440-1681.13396 Text en © 2020 The Authors. Clinical and Experimental Pharmacology and Physiology published by John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Ingvorsen, Camilla
Lelliott, Christopher J.
Brix, Susanne
Hellgren, Lars I.
Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title_full Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title_fullStr Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title_full_unstemmed Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title_short Effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
title_sort effects of maternal high‐fat/high sucrose diet on hepatic lipid metabolism in rat offspring
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818417/
https://www.ncbi.nlm.nih.gov/pubmed/32772427
http://dx.doi.org/10.1111/1440-1681.13396
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