A randomized 3-way crossover study indicates that high-protein feeding induces de novo lipogenesis in healthy humans
BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic lipid accumulation, derived in part from increased de novo lipogenesis. Despite the popularity of high-protein diets for weight loss, the effe...
Saved in:
Published in | JCI insight Vol. 4; no. 12 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Clinical Investigation
20.06.2019
|
Subjects | |
Online Access | Get full text |
ISSN | 2379-3708 2379-3708 |
DOI | 10.1172/jci.insight.124819 |
Cover
Loading…
Abstract | BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic lipid accumulation, derived in part from increased de novo lipogenesis. Despite the popularity of high-protein diets for weight loss, the effect of dietary protein on de novo lipogenesis is poorly studied. We aimed to characterize the effect of dietary protein on de novo lipid synthesis.METHODSWe use a 3-way crossover interventional study in healthy males to determine the effect of high-protein feeding on de novo lipogenesis, combined with in vitro models to determine the lipogenic effects of specific amino acids. The primary outcome was a change in de novo lipogenesis-associated triglycerides in response to protein feeding.RESULTSWe demonstrate that high-protein feeding, rich in glutamate, increases de novo lipogenesis-associated triglycerides in plasma (1.5-fold compared with control; P < 0.0001) and liver-derived very low-density lipoprotein particles (1.8-fold; P < 0.0001) in samples from human subjects (n = 9 per group). In hepatocytes, we show that glutamate-derived carbon is incorporated into triglycerides via palmitate. In addition, supplementation with glutamate, glutamine, and leucine, but not lysine, increased triglyceride synthesis and decreased glucose uptake. Glutamate, glutamine, and leucine increased activation of protein kinase B, suggesting that induction of de novo lipogenesis occurs via the insulin signaling cascade.CONCLUSIONThese findings provide mechanistic insight into how select amino acids induce de novo lipogenesis and insulin resistance, suggesting that high-protein feeding to tackle diabetes and obesity requires greater consideration.FUNDINGThe research was supported by UK Medical Research Council grants MR/P011705/1, MC_UP_A090_1006 and MR/P01836X/1. JLG is supported by the Imperial Biomedical Research Centre, National Institute for Health Research (NIHR). |
---|---|
AbstractList | A subset of amino acids may induce de novo lipogenesis in humans, suggesting that use of high-protein diets to tackle diabetes requires greater consideration. BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic lipid accumulation, derived in part from increased de novo lipogenesis. Despite the popularity of high-protein diets for weight loss, the effect of dietary protein on de novo lipogenesis is poorly studied. We aimed to characterize the effect of dietary protein on de novo lipid synthesis.METHODSWe use a 3-way crossover interventional study in healthy males to determine the effect of high-protein feeding on de novo lipogenesis, combined with in vitro models to determine the lipogenic effects of specific amino acids. The primary outcome was a change in de novo lipogenesis-associated triglycerides in response to protein feeding.RESULTSWe demonstrate that high-protein feeding, rich in glutamate, increases de novo lipogenesis-associated triglycerides in plasma (1.5-fold compared with control; P < 0.0001) and liver-derived very low-density lipoprotein particles (1.8-fold; P < 0.0001) in samples from human subjects (n = 9 per group). In hepatocytes, we show that glutamate-derived carbon is incorporated into triglycerides via palmitate. In addition, supplementation with glutamate, glutamine, and leucine, but not lysine, increased triglyceride synthesis and decreased glucose uptake. Glutamate, glutamine, and leucine increased activation of protein kinase B, suggesting that induction of de novo lipogenesis occurs via the insulin signaling cascade.CONCLUSIONThese findings provide mechanistic insight into how select amino acids induce de novo lipogenesis and insulin resistance, suggesting that high-protein feeding to tackle diabetes and obesity requires greater consideration.FUNDINGThe research was supported by UK Medical Research Council grants MR/P011705/1, MC_UP_A090_1006 and MR/P01836X/1. JLG is supported by the Imperial Biomedical Research Centre, National Institute for Health Research (NIHR). BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic lipid accumulation, derived in part from increased de novo lipogenesis. Despite the popularity of high-protein diets for weight loss, the effect of dietary protein on de novo lipogenesis is poorly studied. We aimed to characterize the effect of dietary protein on de novo lipid synthesis.METHODSWe use a 3-way crossover interventional study in healthy males to determine the effect of high-protein feeding on de novo lipogenesis, combined with in vitro models to determine the lipogenic effects of specific amino acids. The primary outcome was a change in de novo lipogenesis-associated triglycerides in response to protein feeding.RESULTSWe demonstrate that high-protein feeding, rich in glutamate, increases de novo lipogenesis-associated triglycerides in plasma (1.5-fold compared with control; P < 0.0001) and liver-derived very low-density lipoprotein particles (1.8-fold; P < 0.0001) in samples from human subjects (n = 9 per group). In hepatocytes, we show that glutamate-derived carbon is incorporated into triglycerides via palmitate. In addition, supplementation with glutamate, glutamine, and leucine, but not lysine, increased triglyceride synthesis and decreased glucose uptake. Glutamate, glutamine, and leucine increased activation of protein kinase B, suggesting that induction of de novo lipogenesis occurs via the insulin signaling cascade.CONCLUSIONThese findings provide mechanistic insight into how select amino acids induce de novo lipogenesis and insulin resistance, suggesting that high-protein feeding to tackle diabetes and obesity requires greater consideration.FUNDINGThe research was supported by UK Medical Research Council grants MR/P011705/1, MC_UP_A090_1006 and MR/P01836X/1. JLG is supported by the Imperial Biomedical Research Centre, National Institute for Health Research (NIHR).BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic lipid accumulation, derived in part from increased de novo lipogenesis. Despite the popularity of high-protein diets for weight loss, the effect of dietary protein on de novo lipogenesis is poorly studied. We aimed to characterize the effect of dietary protein on de novo lipid synthesis.METHODSWe use a 3-way crossover interventional study in healthy males to determine the effect of high-protein feeding on de novo lipogenesis, combined with in vitro models to determine the lipogenic effects of specific amino acids. The primary outcome was a change in de novo lipogenesis-associated triglycerides in response to protein feeding.RESULTSWe demonstrate that high-protein feeding, rich in glutamate, increases de novo lipogenesis-associated triglycerides in plasma (1.5-fold compared with control; P < 0.0001) and liver-derived very low-density lipoprotein particles (1.8-fold; P < 0.0001) in samples from human subjects (n = 9 per group). In hepatocytes, we show that glutamate-derived carbon is incorporated into triglycerides via palmitate. In addition, supplementation with glutamate, glutamine, and leucine, but not lysine, increased triglyceride synthesis and decreased glucose uptake. Glutamate, glutamine, and leucine increased activation of protein kinase B, suggesting that induction of de novo lipogenesis occurs via the insulin signaling cascade.CONCLUSIONThese findings provide mechanistic insight into how select amino acids induce de novo lipogenesis and insulin resistance, suggesting that high-protein feeding to tackle diabetes and obesity requires greater consideration.FUNDINGThe research was supported by UK Medical Research Council grants MR/P011705/1, MC_UP_A090_1006 and MR/P01836X/1. JLG is supported by the Imperial Biomedical Research Centre, National Institute for Health Research (NIHR). |
Author | Charidemou, Evelina Harvey, Matthew Li, Xuefei Liggi, Sonia Griffin, Julian L. McNally, Ben D. West, James A. Ashmore, Tom Orford, Elise |
AuthorAffiliation | 1 Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom 3 Medical Research Council — Elsie Widdowson Laboratory, Cambridge, United Kingdom 4 Computational and Systems Medicine, Surgery and Cancer, Imperial College London, London, United Kingdom 2 Division of Gastroenterology and Hepatology, Department of Medicine, Addenbrooke’s Hospital, University of Cambridge, Cambridge, United Kingdom |
AuthorAffiliation_xml | – name: 4 Computational and Systems Medicine, Surgery and Cancer, Imperial College London, London, United Kingdom – name: 3 Medical Research Council — Elsie Widdowson Laboratory, Cambridge, United Kingdom – name: 1 Department of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, United Kingdom – name: 2 Division of Gastroenterology and Hepatology, Department of Medicine, Addenbrooke’s Hospital, University of Cambridge, Cambridge, United Kingdom |
Author_xml | – sequence: 1 givenname: Evelina surname: Charidemou fullname: Charidemou, Evelina – sequence: 2 givenname: Tom surname: Ashmore fullname: Ashmore, Tom – sequence: 3 givenname: Xuefei orcidid: 0000-0001-8765-2033 surname: Li fullname: Li, Xuefei – sequence: 4 givenname: Ben D. surname: McNally fullname: McNally, Ben D. – sequence: 5 givenname: James A. surname: West fullname: West, James A. – sequence: 6 givenname: Sonia orcidid: 0000-0003-1802-357X surname: Liggi fullname: Liggi, Sonia – sequence: 7 givenname: Matthew surname: Harvey fullname: Harvey, Matthew – sequence: 8 givenname: Elise surname: Orford fullname: Orford, Elise – sequence: 9 givenname: Julian L. orcidid: 0000-0003-1336-7744 surname: Griffin fullname: Griffin, Julian L. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31145699$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kc1r3DAQxUVJaNIk_0APRcdevNWHLVuXQgj9gkAvyVlMpPFawZa2krxl89fX292UtIeeZmB-7z2Y94achBiQkLecrThvxYdH61c-ZL8eyoqLuuP6FTkXstWVbFl38mI_I1c5PzLGeFsL1nSvyZnkvG6U1uekXNMEwcXJP6GjsvoJO2pTzDluMdFcZrejPjhvoWCmZYBChyWz2qRY0AfaIzof1ntmtgvhkIa4jXT0m7jGgNnn5UYHhLEMOzrME4R8SU57GDNeHecFuf_86e7ma3X7_cu3m-vbytZMlMoptLoTgj-43nGoG211IxslJOqGdbbtFe87xZApW7cCuG4sr0ECgHJM1_KCfDz4buaHCZ3FUBKMZpP8BGlnInjz9yX4wazj1iglNFd8MXh_NEjxx4y5mMlni-MIAeOcjRBSdo1UWi3ou5dZf0KeX70A3QH4_d6EvbG-QPFxH-1Hw5nZF2uWYs2xWHModpGKf6TP7v8R_QL68K0q |
CitedBy_id | crossref_primary_10_1038_s41598_022_05562_8 crossref_primary_10_1097_MOL_0000000000000720 crossref_primary_10_1186_s13098_023_01037_6 crossref_primary_10_2139_ssrn_4199881 crossref_primary_10_1016_j_heliyon_2022_e12294 crossref_primary_10_1111_hepr_13631 crossref_primary_10_3389_fonc_2022_858017 crossref_primary_10_3389_fphys_2022_940974 crossref_primary_10_1093_ajcn_nqac075 crossref_primary_10_3390_jcdd10070282 crossref_primary_10_1007_s00726_022_03131_x crossref_primary_10_1016_j_lfs_2024_122471 crossref_primary_10_1055_a_1917_8335 crossref_primary_10_1038_s41575_021_00472_y crossref_primary_10_1016_j_atherosclerosis_2024_119066 crossref_primary_10_1097_MCO_0000000000000929 crossref_primary_10_1038_s41598_022_14433_1 crossref_primary_10_1210_endocr_bqaa142 crossref_primary_10_3390_nu16203480 crossref_primary_10_3390_cells9071638 crossref_primary_10_1186_s12915_021_01192_0 crossref_primary_10_3390_biology12070949 crossref_primary_10_1038_s41514_024_00183_z crossref_primary_10_1038_s41467_022_34195_8 crossref_primary_10_26599_FSHW_2024_9250031 crossref_primary_10_18632_aging_103218 crossref_primary_10_1002_oby_22964 crossref_primary_10_3390_biomedicines10030550 crossref_primary_10_1002_dmrr_3490 crossref_primary_10_1097_MCO_0000000000000914 crossref_primary_10_1055_a_2145_0934 |
Cites_doi | 10.1093/ajcn/77.1.43 10.1172/JCI32914 10.2337/db11-1355 10.1080/15384101.2015.1123355 10.1007/s11306-018-1349-5 10.2337/diabetes.52.5.1073 10.1038/emm.2015.93 10.3892/etm.2011.328 10.1371/journal.pone.0047303 10.1161/CIRCULATIONAHA.113.002500 10.1186/s13059-018-1439-8 10.1074/jbc.M204681200 10.5812/ijem.4783 10.1021/ac103093w 10.1073/pnas.111138698 10.1002/0471250953.bi1324s46 10.1172/JCI81993 10.1093/ajcn/81.1.35 10.1111/j.1432-1033.1968.tb00376.x 10.1021/ac051437y 10.1016/j.cmet.2016.04.022 10.2337/diab.46.3.393 10.1016/S0021-9258(18)64849-5 10.1093/ajcn/84.2.289 10.1172/JCI23621 10.1097/MOL.0b013e32832b3f4c 10.1210/jc.2008-1595 10.1021/ac202450g 10.1021/bi00516a008 10.1074/jbc.M110.166991 10.1371/journal.pone.0145850 10.1172/JCI118645 10.1002/hep.22887 10.1172/JCI44442 10.1177/1535370216633312 10.1093/ajcn/87.4.817 10.1093/ajcn/73.2.253 10.1186/s12859-015-0562-8 10.1016/j.bbrc.2017.07.116 10.1073/pnas.0706517104 10.1016/j.cmet.2011.06.002 10.1186/1758-2946-4-23 10.1371/journal.pone.0181393 10.1074/jbc.M106703200 10.1039/b816965a 10.1074/jbc.274.2.1092 10.1093/bioinformatics/btn323 10.4254/wjh.v4.i7.209 10.1016/j.cell.2011.06.034 10.1016/j.metabol.2014.03.006 10.1016/S0092-8674(00)80595-4 10.1016/j.bbadis.2013.02.003 10.1172/JCI19992 10.3390/nu8090571 10.1038/nprot.2011.335 |
ContentType | Journal Article |
Copyright | 2019 Charidemou et al. 2019 Charidemou et al. |
Copyright_xml | – notice: 2019 Charidemou et al. 2019 Charidemou et al. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 5PM |
DOI | 10.1172/jci.insight.124819 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
EISSN | 2379-3708 |
ExternalDocumentID | PMC6629161 31145699 10_1172_jci_insight_124819 |
Genre | Randomized Controlled Trial Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Medical Research Council grantid: MR/P011705/1 – fundername: Medical Research Council grantid: MC_UP_A090_1006 – fundername: Department of Health – fundername: Medical Research Council grantid: MR/P01836X/1 – fundername: ; grantid: MR/P01836X/1 – fundername: ; grantid: MR/P011705/1 – fundername: ; grantid: MC_UP_A090_1006 |
GroupedDBID | 53G AAFWJ AAYXX ADBBV AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS CITATION GROUPED_DOAJ HYE M~E OK1 RPM CGR CUY CVF ECM EIF NPM 7X8 5PM |
ID | FETCH-LOGICAL-c402t-d6ec98221bdfd1a459c9535623e9508c7f61f860e06c472a195c14a3aaa6d0943 |
ISSN | 2379-3708 |
IngestDate | Thu Aug 21 18:24:17 EDT 2025 Fri Jul 11 04:24:34 EDT 2025 Sat May 31 02:12:36 EDT 2025 Thu Apr 24 23:02:33 EDT 2025 Tue Jul 01 02:59:28 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 12 |
Keywords | Obesity Diabetes Metabolism Amino acid metabolism |
Language | English |
License | http://creativecommons.org/licenses/by/4.0 This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c402t-d6ec98221bdfd1a459c9535623e9508c7f61f860e06c472a195c14a3aaa6d0943 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ORCID | 0000-0001-8765-2033 0000-0003-1336-7744 0000-0003-1802-357X |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC6629161 |
PMID | 31145699 |
PQID | 2233853696 |
PQPubID | 23479 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_6629161 proquest_miscellaneous_2233853696 pubmed_primary_31145699 crossref_citationtrail_10_1172_jci_insight_124819 crossref_primary_10_1172_jci_insight_124819 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-06-20 |
PublicationDateYYYYMMDD | 2019-06-20 |
PublicationDate_xml | – month: 06 year: 2019 text: 2019-06-20 day: 20 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | JCI insight |
PublicationTitleAlternate | JCI Insight |
PublicationYear | 2019 |
Publisher | American Society for Clinical Investigation |
Publisher_xml | – name: American Society for Clinical Investigation |
References | B20 Tremblay (B26) 2001; 276 B21 B22 B23 B24 B25 B27 B29 Libiseller (B52) 2015; 16 Folch (B47) 1957; 226 B30 B31 B32 B33 B34 B35 B36 B38 Au (B46) 2003; 52 B39 Garcia-Caraballo (B28) 2013; 1832 B2 B3 B4 B5 Varlamov (B17) 2014; 5 B6 B7 B8 B9 B40 B41 B42 B43 B44 B45 B48 Misra (B1) 2008; 93 B50 B51 B53 B10 B54 B11 B55 B12 B56 B13 B57 B14 B58 B15 B16 B18 B19 Holman (B49) 2014; 46 Brun (B37) 1997; 46 |
References_xml | – ident: B5 doi: 10.1093/ajcn/77.1.43 – ident: B41 doi: 10.1172/JCI32914 – ident: B12 doi: 10.2337/db11-1355 – ident: B44 doi: 10.1080/15384101.2015.1123355 – ident: B55 doi: 10.1007/s11306-018-1349-5 – volume: 52 start-page: 1073 year: 2003 ident: B46 article-title: Regulation of microsomal triglyceride transfer protein gene by insulin in HepG2 cells: roles of MAPKerk and MAPKp38 publication-title: Diabetes doi: 10.2337/diabetes.52.5.1073 – ident: B30 doi: 10.1038/emm.2015.93 – ident: B40 doi: 10.3892/etm.2011.328 – ident: B16 doi: 10.1371/journal.pone.0047303 – ident: B19 doi: 10.1161/CIRCULATIONAHA.113.002500 – ident: B9 doi: 10.1186/s13059-018-1439-8 – ident: B24 doi: 10.1074/jbc.M204681200 – volume: 5 year: 2014 ident: B17 article-title: Sex-specific differences in lipid and glucose metabolism publication-title: Front Endocrinol (Lausanne) – ident: B58 – ident: B18 doi: 10.5812/ijem.4783 – ident: B48 doi: 10.1021/ac103093w – ident: B36 doi: 10.1073/pnas.111138698 – volume: 46 start-page: 13.24.1 year: 2014 ident: B49 article-title: Employing ProteoWizard to convert raw mass spectrometry data publication-title: Curr Protoc Bioinformatics doi: 10.1002/0471250953.bi1324s46 – ident: B7 doi: 10.1172/JCI81993 – ident: B10 doi: 10.1093/ajcn/81.1.35 – ident: B23 doi: 10.1111/j.1432-1033.1968.tb00376.x – ident: B51 – ident: B53 doi: 10.1021/ac051437y – ident: B8 doi: 10.1016/j.cmet.2016.04.022 – volume: 46 start-page: 393 issue: 3 year: 1997 ident: B37 article-title: Long-chain fatty acids inhibit acetyl-CoA carboxylase gene expression in the pancreatic β-cell line INS-1 publication-title: Diabetes doi: 10.2337/diab.46.3.393 – volume: 226 start-page: 497 issue: 1 year: 1957 ident: B47 article-title: A simple method for the isolation and purification of total lipides from animal tissue publication-title: J Biol Chem doi: 10.1016/S0021-9258(18)64849-5 – ident: B2 doi: 10.1093/ajcn/84.2.289 – ident: B4 doi: 10.1172/JCI23621 – ident: B39 doi: 10.1097/MOL.0b013e32832b3f4c – volume: 93 start-page: 9 year: 2008 ident: B1 article-title: Obesity and the metabolic syndrome in developing countries publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2008-1595 – ident: B54 doi: 10.1021/ac202450g – ident: B22 doi: 10.1021/bi00516a008 – ident: B34 doi: 10.1074/jbc.M110.166991 – ident: B14 doi: 10.1371/journal.pone.0145850 – ident: B11 doi: 10.1172/JCI118645 – ident: B32 doi: 10.1002/hep.22887 – ident: B20 doi: 10.1172/JCI44442 – ident: B27 doi: 10.1177/1535370216633312 – ident: B21 doi: 10.1093/ajcn/87.4.817 – ident: B6 doi: 10.1093/ajcn/73.2.253 – volume: 16 year: 2015 ident: B52 article-title: IPO: a tool for automated optimization of XCMS parameters publication-title: BMC Bioinformatics doi: 10.1186/s12859-015-0562-8 – ident: B43 doi: 10.1016/j.bbrc.2017.07.116 – ident: B15 doi: 10.1073/pnas.0706517104 – ident: B25 doi: 10.1016/j.cmet.2011.06.002 – ident: B57 doi: 10.1186/1758-2946-4-23 – ident: B38 doi: 10.1371/journal.pone.0181393 – volume: 276 start-page: 38052 issue: 41 year: 2001 ident: B26 article-title: Amino acid and insulin signaling via the mTOR/p70 S6 kinase pathway: a negative feedback mechanism leading to insulin resistance in skeletal muscle cells publication-title: J Biol Chem doi: 10.1074/jbc.M106703200 – ident: B31 doi: 10.1039/b816965a – ident: B35 doi: 10.1074/jbc.274.2.1092 – ident: B50 doi: 10.1093/bioinformatics/btn323 – ident: B3 doi: 10.4254/wjh.v4.i7.209 – ident: B33 doi: 10.1016/j.cell.2011.06.034 – ident: B13 doi: 10.1016/j.metabol.2014.03.006 – ident: B45 doi: 10.1016/S0092-8674(00)80595-4 – volume: 1832 start-page: 685 issue: 5 year: 2013 ident: B28 article-title: Prevention and reversal of hepatic steatosis with a high-protein diet in mice publication-title: Biochim Biophys Acta doi: 10.1016/j.bbadis.2013.02.003 – ident: B42 doi: 10.1172/JCI19992 – ident: B29 doi: 10.3390/nu8090571 – ident: B56 doi: 10.1038/nprot.2011.335 |
SSID | ssj0001742058 |
Score | 2.2705698 |
Snippet | BACKGROUNDDietary changes have led to the growing prevalence of type 2 diabetes and nonalcoholic fatty liver disease. A hallmark of both disorders is hepatic... A subset of amino acids may induce de novo lipogenesis in humans, suggesting that use of high-protein diets to tackle diabetes requires greater consideration. |
SourceID | pubmedcentral proquest pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
SubjectTerms | Administration, Oral Adult Amino Acids - administration & dosage Amino Acids - adverse effects Clinical Medicine Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - prevention & control Diet, High-Protein - adverse effects Dietary Proteins - administration & dosage Dietary Proteins - adverse effects Feeding Behavior - physiology Healthy Volunteers Hepatocytes - metabolism Humans Insulin - metabolism Insulin Resistance - physiology Lipogenesis Liver - cytology Liver - metabolism Male Non-alcoholic Fatty Liver Disease - metabolism Non-alcoholic Fatty Liver Disease - prevention & control Obesity - etiology Obesity - metabolism Triglycerides - biosynthesis Triglycerides - blood Young Adult |
Title | A randomized 3-way crossover study indicates that high-protein feeding induces de novo lipogenesis in healthy humans |
URI | https://www.ncbi.nlm.nih.gov/pubmed/31145699 https://www.proquest.com/docview/2233853696 https://pubmed.ncbi.nlm.nih.gov/PMC6629161 |
Volume | 4 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb5wwELa26aWXqlVfmz7kSr0htmCMgeMqbZVWSk4baW_IYNNQpRBlIVVyqPrTO2MDC8m2anpBK2Nbhvl2PGO-mSHkXeZJCVDgeFAlXLBvYzdOFHfDPCt0XLAoVhjvfHQsDk_4l3W4ns1-jVhLbZMt8uudcSX_I1VoA7lilOwdJDtMCg3wG-QLV5AwXP9JxksHdhpVfy-vwWwM3B_yyjG7HtIybeJYBz9JI-lpAxambBzMTuya3Axl5RR258I-LRKzlHaq-rJ2zsrz-ivqwNKQZW2o5JUt57eZWLMHn5HMjv79iCZwgTVn69Zo2UsMdx80_3Jz2vN6V_Z1GC6QIRSsW13ocntMeCz7Iti6cj4sxqcTGBAlXOZtlRgLogSUmGd1rN7R1mlhPgYb263cI0wW-y0vF92jLcA4iTuNO8mkfWOHG3iHxuOJWApzpN0cqZ3jHrnPwNFA1X70c3RKF3HmmSKvw6L7yKuIvb-9lKl1c8tlucm8HZkyq0fkYeeD0KUF1GMy09UT0izpFkzUgIkOYKIGTHQAE0Uw0TGYaAcm2oGJKk0RTHQEJrhHOzBRC6an5OTTx9XBoduV5HBz7rHGVULnmPHRz1ShfMnDJE_CAG1ojeWE86gQfhELT3si5xGTfhLmPpeBlFIoJLE-I3tVXekXhIIf4YtIwSUIOINRgQoT2F1YEEoO-m1O_P5VpnmXrx7Lppylf5binDjDmHObreWvvd_2EkpBqeKXMlnput2kYDMHYMeKRMzJcyuxYb7A98HpSGB0NJHl0AETtk_vVOWpSdwuBANvzN-_0ypfkgfbP9YrstdctPo1GMJN9sZg9TdTDrwb |
linkProvider | ISSN International Centre |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+randomized+3-way+crossover+study+indicates+that+high-protein+feeding+induces+de+novo+lipogenesis+in+healthy+humans&rft.jtitle=JCI+insight&rft.au=Charidemou%2C+Evelina&rft.au=Ashmore%2C+Tom&rft.au=Li%2C+Xuefei&rft.au=McNally%2C+Ben+D.&rft.date=2019-06-20&rft.issn=2379-3708&rft.eissn=2379-3708&rft.volume=4&rft.issue=12&rft_id=info:doi/10.1172%2Fjci.insight.124819&rft.externalDBID=n%2Fa&rft.externalDocID=10_1172_jci_insight_124819 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2379-3708&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2379-3708&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2379-3708&client=summon |