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 |
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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. 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.</description><identifier>ISSN: 0023-6837</identifier><identifier>EISSN: 1530-0307</identifier><identifier>DOI: 10.1038/s41374-019-0344-4</identifier><identifier>PMID: 31748681</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>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</subject><ispartof>Laboratory investigation, 2020-04, Vol.100 (4), p.553-569</ispartof><rights>2019 United States & Canadian Academy of Pathology</rights><rights>The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2019</rights><rights>2019© The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2019</rights><rights>The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2019.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-ba736b8340ad3e1d7c0ff2019153bdb5c61155410f231ba6291b89631bf0203e3</citedby><cites>FETCH-LOGICAL-c550t-ba736b8340ad3e1d7c0ff2019153bdb5c61155410f231ba6291b89631bf0203e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31748681$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Peng, Hui</creatorcontrib><creatorcontrib>Xu, Huiting</creatorcontrib><creatorcontrib>Li, Jiangyuan</creatorcontrib><creatorcontrib>Golovko, Mikhail</creatorcontrib><creatorcontrib>Cheng, Henghui</creatorcontrib><creatorcontrib>Lynch, Ernest C.</creatorcontrib><creatorcontrib>Liu, Lin</creatorcontrib><creatorcontrib>McCauley, Naomi</creatorcontrib><creatorcontrib>Kennedy, Lindsey</creatorcontrib><creatorcontrib>Alpini, Gianfranco</creatorcontrib><creatorcontrib>Zhang, Ke K.</creatorcontrib><creatorcontrib>Xie, Linglin</creatorcontrib><title>Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver</title><title>Laboratory investigation</title><addtitle>Lab Invest</addtitle><addtitle>Lab Invest</addtitle><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.</description><subject>13/1</subject><subject>38/77</subject><subject>38/90</subject><subject>38/91</subject><subject>631/337</subject><subject>64/60</subject><subject>692/699/1702</subject><subject>82/29</subject><subject>AKT protein</subject><subject>AMP</subject><subject>AMP-activated protein kinase</subject><subject>AMP-Activated Protein Kinases - metabolism</subject><subject>Animals</subject><subject>Cholesterol</subject><subject>Diet</subject><subject>Diet, High-Fat</subject><subject>Fatty acid composition</subject><subject>Fatty acids</subject><subject>Fatty liver</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glucose tolerance</subject><subject>High fat diet</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Intervention</subject><subject>Intolerance</subject><subject>Kinases</subject><subject>Laboratory Medicine</subject><subject>Lactation</subject><subject>Lipid metabolism</subject><subject>Lipid Metabolism - genetics</subject><subject>Lipid Metabolism - physiology</subject><subject>Lipids</subject><subject>Lipogenesis</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Maternal Nutritional Physiological Phenomena - physiology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Non-alcoholic Fatty Liver Disease - metabolism</subject><subject>Offspring</subject><subject>Overnutrition</subject><subject>Oxidation</subject><subject>Pathology</subject><subject>Pregnancy</subject><subject>Proteins</subject><subject>Risk</subject><subject>Signaling</subject><subject>Steatosis</subject><subject>Transcriptome</subject><subject>Weight Gain - physiology</subject><issn>0023-6837</issn><issn>1530-0307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UU1v1DAQtRCIbgs_gAuKxIVL2nHsxI6QkFAFLVIRF-BqOc5kcZXYi51dqf--E6WUj8OePLbfe_NmHmOvOJxzEPoiSy6ULIG3JQgpS_mEbXgtgG6gnrINQCXKRgt1wk5zvgXgUjb1c3YiuJK60XzDfnyxM6Zgx6L3OBc-0O2AYfYxFB0OMWGxS7gNNrg7qvyEuYjDkKkM22L0O98XE862i6PPE_Hp7YDpBXs22DHjy4fzjH3_9PHb5XV58_Xq8-WHm9LVNcxlZ5VoOi0k2F4g75WDYahoHpqi67vaNZzXteQwVIJ3tqla3um2oXqACgSKM_Z-1d3tuwl7R86THc1i1KY7E603__4E_9Ns48EoDlVbaRJ4-yCQ4q895tlMPjscRxsw7rOhvo3S5GCBvvkPehv3y-oIJZVstapVfRQltAAA3SwovqJcijknHB4tczBLtmbN1tAuzJKtkcR5_fesj4zfYRKgWgFrOpj-tD6m-m4lIcV08ETKzmNw2PuEbjZ99EfY9-_Bwi8</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Zhou, Yi</creator><creator>Peng, Hui</creator><creator>Xu, Huiting</creator><creator>Li, Jiangyuan</creator><creator>Golovko, Mikhail</creator><creator>Cheng, Henghui</creator><creator>Lynch, Ernest C.</creator><creator>Liu, Lin</creator><creator>McCauley, Naomi</creator><creator>Kennedy, Lindsey</creator><creator>Alpini, Gianfranco</creator><creator>Zhang, Ke K.</creator><creator>Xie, Linglin</creator><general>Elsevier Inc</general><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200401</creationdate><title>Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-ba736b8340ad3e1d7c0ff2019153bdb5c61155410f231ba6291b89631bf0203e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>13/1</topic><topic>38/77</topic><topic>38/90</topic><topic>38/91</topic><topic>631/337</topic><topic>64/60</topic><topic>692/699/1702</topic><topic>82/29</topic><topic>AKT protein</topic><topic>AMP</topic><topic>AMP-activated protein kinase</topic><topic>AMP-Activated Protein Kinases - 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metabolism</topic><topic>Offspring</topic><topic>Overnutrition</topic><topic>Oxidation</topic><topic>Pathology</topic><topic>Pregnancy</topic><topic>Proteins</topic><topic>Risk</topic><topic>Signaling</topic><topic>Steatosis</topic><topic>Transcriptome</topic><topic>Weight Gain - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Yi</creatorcontrib><creatorcontrib>Peng, Hui</creatorcontrib><creatorcontrib>Xu, Huiting</creatorcontrib><creatorcontrib>Li, Jiangyuan</creatorcontrib><creatorcontrib>Golovko, Mikhail</creatorcontrib><creatorcontrib>Cheng, Henghui</creatorcontrib><creatorcontrib>Lynch, Ernest C.</creatorcontrib><creatorcontrib>Liu, Lin</creatorcontrib><creatorcontrib>McCauley, Naomi</creatorcontrib><creatorcontrib>Kennedy, Lindsey</creatorcontrib><creatorcontrib>Alpini, Gianfranco</creatorcontrib><creatorcontrib>Zhang, Ke K.</creatorcontrib><creatorcontrib>Xie, Linglin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Laboratory investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Yi</au><au>Peng, Hui</au><au>Xu, Huiting</au><au>Li, Jiangyuan</au><au>Golovko, Mikhail</au><au>Cheng, Henghui</au><au>Lynch, Ernest C.</au><au>Liu, Lin</au><au>McCauley, Naomi</au><au>Kennedy, Lindsey</au><au>Alpini, Gianfranco</au><au>Zhang, Ke K.</au><au>Xie, Linglin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal diet intervention before pregnancy primes offspring lipid metabolism in liver</atitle><jtitle>Laboratory investigation</jtitle><stitle>Lab Invest</stitle><addtitle>Lab Invest</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>100</volume><issue>4</issue><spage>553</spage><epage>569</epage><pages>553-569</pages><issn>0023-6837</issn><eissn>1530-0307</eissn><abstract>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.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><pmid>31748681</pmid><doi>10.1038/s41374-019-0344-4</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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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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