Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver

Nonalcoholic fatty liver disease (NAFLD) has a developmental origin and is influenced in utero. We aimed to evaluate if maternal diet intervention before pregnancy would be beneficial to reduce the risk of offspring NAFLD. In our study, female mice were either on a normal-fat diet (NF group), or a h...

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Veröffentlicht in:Laboratory investigation 2020-04, Vol.100 (4), p.553-569
Hauptverfasser: Zhou, Yi, Peng, Hui, Xu, Huiting, Li, Jiangyuan, Golovko, Mikhail, Cheng, Henghui, Lynch, Ernest C., Liu, Lin, McCauley, Naomi, Kennedy, Lindsey, Alpini, Gianfranco, Zhang, Ke K., Xie, Linglin
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container_issue 4
container_start_page 553
container_title Laboratory investigation
container_volume 100
creator Zhou, Yi
Peng, Hui
Xu, Huiting
Li, Jiangyuan
Golovko, Mikhail
Cheng, Henghui
Lynch, Ernest C.
Liu, Lin
McCauley, Naomi
Kennedy, Lindsey
Alpini, Gianfranco
Zhang, Ke K.
Xie, Linglin
description Nonalcoholic fatty liver disease (NAFLD) has a developmental origin and is influenced in utero. We aimed to evaluate if maternal diet intervention before pregnancy would be beneficial to reduce the risk of offspring NAFLD. In our study, female mice were either on a normal-fat diet (NF group), or a high-fat diet for 12 weeks and continued on this diet throughout pregnancy and lactation (HF group), or switched from HF-to-NF diet 1 week (H1N group), or 9 weeks (H9N group) before pregnancy. Compared with the NF offspring, the H1N and HF, but not the H9N offspring, displayed more severe hepatic steatosis and glucose intolerance. More specifically, an abnormal blood lipid panel was seen in the H1N offspring and abnormal hepatic free fatty acid composition was present in both the HF and H1N offspring, while the H9N offspring displayed both at normal levels. These physiological changes were associated with desensitized hepatic insulin/AKT signaling, increased expression of genes and proteins for de novo lipogenesis and cholesterol synthesis, decreased expression of genes and proteins for fatty acid oxidation, increased Pcsk9 expression, and hypoactivation of 5′ AMP-activated protein kinase (AMPK) signaling in the HF and H1N offspring. However, these effects were completely or partially rescued in the H9N offspring. In summary, we found that early maternal diet intervention is effective in reducing the risk of offspring NAFLD caused by maternal HF diet. These findings provide significant support to develop effective diet intervention strategies and policies for prevention of obesity and NAFLD to promote optimal health outcomes for mothers and children.
doi_str_mv 10.1038/s41374-019-0344-4
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We aimed to evaluate if maternal diet intervention before pregnancy would be beneficial to reduce the risk of offspring NAFLD. In our study, female mice were either on a normal-fat diet (NF group), or a high-fat diet for 12 weeks and continued on this diet throughout pregnancy and lactation (HF group), or switched from HF-to-NF diet 1 week (H1N group), or 9 weeks (H9N group) before pregnancy. Compared with the NF offspring, the H1N and HF, but not the H9N offspring, displayed more severe hepatic steatosis and glucose intolerance. More specifically, an abnormal blood lipid panel was seen in the H1N offspring and abnormal hepatic free fatty acid composition was present in both the HF and H1N offspring, while the H9N offspring displayed both at normal levels. These physiological changes were associated with desensitized hepatic insulin/AKT signaling, increased expression of genes and proteins for de novo lipogenesis and cholesterol synthesis, decreased expression of genes and proteins for fatty acid oxidation, increased Pcsk9 expression, and hypoactivation of 5′ AMP-activated protein kinase (AMPK) signaling in the HF and H1N offspring. However, these effects were completely or partially rescued in the H9N offspring. In summary, we found that early maternal diet intervention is effective in reducing the risk of offspring NAFLD caused by maternal HF diet. 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subjects 13/1
38/77
38/90
38/91
631/337
64/60
692/699/1702
82/29
AKT protein
AMP
AMP-activated protein kinase
AMP-Activated Protein Kinases - metabolism
Animals
Cholesterol
Diet
Diet, High-Fat
Fatty acid composition
Fatty acids
Fatty liver
Female
Gene expression
Genes
Glucose tolerance
High fat diet
Insulin
Insulin - metabolism
Intervention
Intolerance
Kinases
Laboratory Medicine
Lactation
Lipid metabolism
Lipid Metabolism - genetics
Lipid Metabolism - physiology
Lipids
Lipogenesis
Liver
Liver - metabolism
Liver diseases
Male
Maternal Nutritional Physiological Phenomena - physiology
Medicine
Medicine & Public Health
Metabolism
Mice
Non-alcoholic Fatty Liver Disease - metabolism
Offspring
Overnutrition
Oxidation
Pathology
Pregnancy
Proteins
Risk
Signaling
Steatosis
Transcriptome
Weight Gain - physiology
title Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver
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