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Research Article

Low-fat diet, and medium-fat diets containing coconut oil and soybean oil exert different metabolic effects in untrained and treadmill-trained mice

Mark Christian Manio1 Department of Food Science and Biotechnology, Graduate School of AgricultureKyoto UniversityKyotoJapan

Shigenobu Matsumura1 Department of Food Science and Biotechnology, Graduate School of AgricultureKyoto UniversityKyotoJapan

Kazuo Inoue1 Department of Food Science and Biotechnology, Graduate School of AgricultureKyoto UniversityKyotoJapanCorrespondence[email protected]

Article: 29 | Published online: 01 Apr 2022

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https://doi.org/10.1186/s12970-018-0234-y
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References

Amri IN. The Lauric (coconut and palm kernel) oils. In: Gunstone FD, editor. Vegetable oils in food technology. West Sussex: Wiley-Blackwell; 2011. p. 169–97.
Google Scholar
DayritFMThe properties of Lauric acid and their significance in coconut oilJ Am Oil Chem Soc201592 1 15 https://doi.org/10.1007/s11746-014-2562-7 1:CAS:528:DC%2BC2cXhvFCgu7zI
Web of Science ®Google Scholar
WangJWangXLiJChenYYangWZhangLEffects of dietary coconut oil as a medium-chain fatty acid source on performance, carcass composition and serum lipids in male broilersAsian-Australas J Anim Sci201528 223 230 https://doi.org/10.5713/ajas.14.0328 25557818 4283167 1:CAS:528:DC%2BC2MXis1KqsLo%3D
PubMedGoogle Scholar
Wang T. Soybean Oil. In: Gunstone FD, editor. Vegetable oils in food technology. West Sussex: Wiley-Blackwell; 2011. p. 59–105.
Google Scholar
GrootPHEHülsmannWCThe activation and oxidation of octanoate and palmitate by rat skeletal muscle mitochondriaBiochim Biophys Acta BBA - Lipids Lipid Metab1973316 124 135 https://doi.org/10.1016/0005-2760(73)90002-7 1:CAS:528:DyaE3sXlsVemtLs%3D
Web of Science ®Google Scholar
CrozierGLMedium-chain triglyceride feeding over the long term: the metabolic fate of [14C]octanoate and [14C]oleate in isolated rat hepatocytesJ Nutr1988118 297 304 https://doi.org/10.1093/jn/118.3.297 3127554 1:CAS:528:DyaL1cXitVelu7k%3D
PubMed Web of Science ®Google Scholar
PégorierJPDuéePHHerbinCLaulanPYBladéCPeretJ et al Fatty acid metabolism in hepatocytes isolated from rats adapted to high-fat diets containing long- or medium-chain triacylglycerolsBiochem J1988249 801 806 https://doi.org/10.1042/bj2490801 3355499 1148777
PubMedGoogle Scholar
EganBZierathJRExercise metabolism and the molecular regulation of skeletal muscle adaptationCell Metab201317 162 184 https://doi.org/10.1016/j.cmet.2012.12.012 23395166 1:CAS:528:DC%2BC3sXitFCnsb4%3D
PubMed Web of Science ®Google Scholar
FanWEvansRPPARs and ERRs: molecular mediators of mitochondrial metabolismCurr Opin Cell Biol201533 49 54 https://doi.org/10.1016/j.ceb.2014.11.002 25486445 1:CAS:528:DC%2BC2cXitVSgurfF
PubMed Web of Science ®Google Scholar
GeorgiadiAKerstenSMechanisms of gene regulation by fatty acidsAdv Nutr Int Rev J20123 127 134 https://doi.org/10.3945/an.111.001602 1:CAS:528:DC%2BC38XmtVGrs78%3D
Web of Science ®Google Scholar
KliewerSASundsethSSJonesSABrownPJWiselyGBKobleCS et al Fatty acids and eicosanoids regulate gene expression through direct interactions with peroxisome proliferator-activated receptors alpha andgamma Proc Natl Acad Sci U S A199794 4318 4323 https://doi.org/10.1073/pnas.94.9.4318 9113987 1:CAS:528:DyaK2sXjtVyht7w%3D
PubMed Web of Science ®Google Scholar
XuHELambertMHMontanaVGParksDJBlanchardSGBrownPJ et al Molecular recognition of fatty acids by peroxisome proliferator-activated receptorsMol Cell19993 397 403 https://doi.org/10.1016/S1097-2765(00)80467-0 10198642 1:CAS:528:DyaK1MXit1OmsLY%3D
PubMed Web of Science ®Google Scholar
LiberatoMVNascimentoASAyersSDLinJZCvoroASilveiraRL et al Medium chain fatty acids are selective peroxisome proliferator activated receptor (PPAR) γ activators and pan-PPAR partial agonistsPLoS One20127 e36297 https://doi.org/10.1371/journal.pone.0036297 22649490 3359336 1:CAS:528:DC%2BC38XotVyqs7o%3D
PubMed Web of Science ®Google Scholar
MalapakaRRVKhooSZhangJChoiJHZhouXEXuY et al Identification and mechanism of 10-carbon fatty acid as modulating ligand of peroxisome proliferator-activated receptorsJ Biol Chem2012287 183 195 https://doi.org/10.1074/jbc.M111.294785 22039047 1:CAS:528:DC%2BC38XotVSh
PubMed Web of Science ®Google Scholar
MontgomeryMKOsborneBBrownSHJSmallLMitchellTWCooneyGJ et al Contrasting metabolic effects of medium- versus long-chain fatty acids in skeletal muscleJ Lipid Res201354 3322 3333 https://doi.org/10.1194/jlr.M040451 24078708 3826680 1:CAS:528:DC%2BC3sXhslKqurjP
PubMedGoogle Scholar
LimJ-HGerhart-HinesZDominyJELeeYKimSTabataM et al Oleic acid stimulates complete oxidation of fatty acids through protein kinase A-dependent activation of SIRT1-PGC1α complexJ Biol Chem2013288 7117 7126 https://doi.org/10.1074/jbc.M112.415729 23329830 3591621 1:CAS:528:DC%2BC3sXjslegsrg%3D
PubMed Web of Science ®Google Scholar
TurnerNHariharanKTidAngJFrangioudakisGBealeSMWrightLE et al Enhancement of muscle mitochondrial oxidative capacity and alterations in insulin action are lipid species dependentDiabetes200958 2547 2554 https://doi.org/10.2337/db09-0784 19720794 2768163 1:CAS:528:DC%2BD1MXhsVCht77O
PubMedGoogle Scholar
GreschikHWurtzJ-MSanglierSBourguetWvan DorsselaerAMorasD et al Structural and functional evidence for ligand-independent transcriptional activation by the estrogen-related receptor 3Mol Cell20029 303 313 https://doi.org/10.1016/S1097-2765(02)00444-6 11864604 1:CAS:528:DC%2BD38XhvFKhu7g%3D
PubMed Web of Science ®Google Scholar
WillyPJMurrayIRQianJBuschBBStevensWCMartinR et al Regulation of PPARγ coactivator 1α (PGC-1α) signaling by an estrogen-related receptor α (ERRα) ligandProc Natl Acad Sci U S A2004101 8912 8917 https://doi.org/10.1073/pnas.0401420101 15184675 428446 1:CAS:528:DC%2BD2cXltlWqsr0%3D
PubMed Web of Science ®Google Scholar
FushikiTMatsumotoKInoueKKawadaTSugimotoESwimming endurance capacity of mice is increased by chronic consumption of medium-chain triglyceridesJ Nutr1995125 531 539 7876928 1:CAS:528:DyaK2MXktFClsL8%3D
PubMed Web of Science ®Google Scholar
OoyamaKWuJNosakaNAoyamaTKasaiMCombined intervention of medium-chain triacylglycerol diet and exercise reduces body fat mass and enhances energy expenditure in ratsJ Nutr Sci Vitaminol (Tokyo)200854 136 141 https://doi.org/10.3177/jnsv.54.136 1:CAS:528:DC%2BD1cXmtFarsrY%3D
PubMed Web of Science ®Google Scholar
MurrayAJKnightNSLittleSECochlinLEClementsMClarkeKDietary long-chain, but not medium-chain, triglycerides impair exercise performance and uncouple cardiac mitochondria in ratsNutr Metab20118 55 https://doi.org/10.1186/1743-7075-8-55 1:CAS:528:DC%2BC3MXhtFCkurrL
Google Scholar
Manio MCC, Matsumura S, Masuda D, Inoue K. CD36 is essential for endurance improvement, changes in whole-body metabolism, and efficient PPAR-related transcriptional responses in the muscle with exercise training. Physiol Rep. 2017;5 https://doi.org/https://doi.org/10.14814/phy2.13282.
Google Scholar
Manio MCC, Inoue K, Fujitani M, Matsumura S, Fushiki T. Combined pharmacological activation of AMPK and PPAR δ potentiates the effects of exercise in trained mice. Physiol Rep. 2016;4 https://doi.org/https://doi.org/10.14814/phy2.12625.
Google Scholar
FolchJLeesMGHSSA simple method for the isolation and purification of total lipides from animal tissuesJ Biol Chem1957226 497 509 13428781 1:STN:280:DyaG2s%2FnsFCjtw%3D%3D
PubMed Web of Science ®Google Scholar
GoodCAKramerHSomogyiMThe determination of glycogenJ Biol Chem1933100 485 491 1:CAS:528:DyaA3sXjvVOgtQ%3D%3D
Google Scholar
SahyunMAlsbergCLStudies on glycogen the hydrolysis of glycogen in various concentrations of acids, and the hydrolysis of glycogen with TakadiastaseJ Biol Chem193193 235 254 1:CAS:528:DyaA38XjvFaj
Google Scholar
HollowayGPThrushABHeigenhauserGJFTandonNNDyckDJBonenA et al Skeletal muscle mitochondrial FAT/CD36 content and palmitate oxidation are not decreased in obese womenAm J Physiol Endocrinol Metab2007292 E1782 E1789 https://doi.org/10.1152/ajpendo.00639.2006 17311893 1:CAS:528:DC%2BD2sXmvF2mtb4%3D
PubMedGoogle Scholar
WilliamsonDHBatesMWPageMAKrebsHAActivities of enzymes involved in acetoacetate utilization in adult mammalian tissuesBiochem J1971121 41 47 https://doi.org/10.1042/bj1210041 5165621 1176484 1:CAS:528:DyaE3MXosV2itw%3D%3D
PubMed Web of Science ®Google Scholar
Srere PA. Citrate synthase: [EC 4.1.3.7. Citrate oxaloacetate-lyase (CoA-acetylating)]. Pp. 3–11 in J. M. Lowenstein, ed., Methods in enzymology, citric acid cycle. New York: Academic Press; 1969.
Google Scholar
MacArthurDGSetoJTChanSQuinlanKGRRafteryJMTurnerN et al An Actn3 knockout mouse provides mechanistic insights into the association between alpha-actinin-3 deficiency and human athletic performanceHum Mol Genet200817 1076 1086 https://doi.org/10.1093/hmg/ddm380 18178581 1:CAS:528:DC%2BD1cXktlSkurw%3D
PubMed Web of Science ®Google Scholar
SpinazziMCasarinAPertegatoVSalviatiLAngeliniCAssessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cellsNat Protoc20127 1235 1246 https://doi.org/10.1038/nprot.2012.058 22653162 1:CAS:528:DC%2BC38XnslWgtrg%3D
PubMed Web of Science ®Google Scholar
WilliamsonDHBatesMWKrebsHAActivity and intracellular distribution of enzymes of ketone-body metabolism in rat liverBiochem J1968108 353 361 https://doi.org/10.1042/bj1080353 5667251 1198819 1:CAS:528:DyaF1cXksVaitb0%3D
PubMed Web of Science ®Google Scholar
CappelliKFelicettiMCapomaccioSSpinsantiGSilvestrelliMSuppliziAVExercise induced stress in horses: selection of the most stable reference genes for quantitative RT-PCR normalizationBMC Mol Biol20089 49 https://doi.org/10.1186/1471-2199-9-49 18489742 2412902 1:CAS:528:DC%2BD1cXovVamsb8%3D
PubMedGoogle Scholar
LarsenSNielsenJHansenCNNielsenLBWibrandFStrideN et al Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjectsJ Physiol2012590 3349 3360 https://doi.org/10.1113/jphysiol.2012.230185 22586215 3459047 1:CAS:528:DC%2BC38Xht1Oks7bI
PubMed Web of Science ®Google Scholar
FukaoTLopaschukGDMitchellGAPathways and control of ketone body metabolism: on the fringe of lipid biochemistryProstaglandins Leukot Essent Fatty Acids200470 243 251 https://doi.org/10.1016/j.plefa.2003.11.001 14769483 1:CAS:528:DC%2BD2cXhtVOksrc%3D
PubMed Web of Science ®Google Scholar
LiYParkJ-SDengJ-HBaiYCytochrome c oxidase subunit IV is essential for assembly and respiratory function of the enzyme complexJ Bioenerg Biomembr200638 283 291 https://doi.org/10.1007/s10863-006-9052-z 17091399 1885940 1:CAS:528:DC%2BD28XhtlSqtb7E
PubMed Web of Science ®Google Scholar
BadmanMKPissiosPKennedyARKoukosGFlierJSMaratos-FlierEHepatic fibroblast growth factor 21 is regulated by PPARα and is a key mediator of hepatic lipid metabolism in Ketotic statesCell Metab20075 426 437 https://doi.org/10.1016/j.cmet.2007.05.002 17550778 1:CAS:528:DC%2BD2sXmslOqsrY%3D
PubMed Web of Science ®Google Scholar
MizunoyaWIwamotoYShirouchiBSatoMKomiyaYRazinFR et al Dietary fat influences the expression of contractile and metabolic genes in rat skeletal musclePLoS One20138 e80152 https://doi.org/10.1371/journal.pone.0080152 24244634 3823866 1:CAS:528:DC%2BC3sXhslylsL7O
PubMedGoogle Scholar
PatsourisDReddyJKMüllerMKerstenSPeroxisome proliferator-activated receptor alpha mediates the effects of high-fat diet on hepatic gene expressionEndocrinology2006147 1508 1516 https://doi.org/10.1210/en.2005-1132 16357043 1:CAS:528:DC%2BD28XhvFygur8%3D
PubMed Web of Science ®Google Scholar
HillAMBuckleyJDMurphyKJHowePRCombining fish-oil supplements with regular aerobic exercise improves body composition and cardiovascular disease risk factorsAm J Clin Nutr200785 1267 1274 https://doi.org/10.1093/ajcn/85.5.1267 17490962 1:CAS:528:DC%2BD2sXls1KiurY%3D
PubMed Web of Science ®Google Scholar
SimiBSemporeBMayetMHFavierRJAdditive effects of training and high-fat diet on energy metabolism during exerciseJ Appl Physiol199171 197 203 https://doi.org/10.1152/jappl.1991.71.1.197 1917743 1:STN:280:DyaK38%2FhtFaitw%3D%3D
PubMed Web of Science ®Google Scholar
BachACIngenbleekYFreyAThe usefulness of dietary medium-chain triglycerides in body weight control: fact or fancy?J Lipid Res199637 708 726 8732772 1:CAS:528:DyaK28XivVOmsro%3D
PubMed Web of Science ®Google Scholar
HildebrandtALPilegaardHNeuferPDDifferential transcriptional activation of select metabolic genes in response to variations in exercise intensity and durationAm J Physiol - Endocrinol Metab2003285 E1021 E1027 https://doi.org/10.1152/ajpendo.00234.2003 12902322 1:CAS:528:DC%2BD3sXpt1Kjur8%3D
PubMed Web of Science ®Google Scholar
PilegaardHOrdwayGASaltinBNeuferPDTranscriptional regulation of gene expression in human skeletal muscle during recovery from exerciseAm J Physiol - Endocrinol Metab2000279 E806 E814 https://doi.org/10.1152/ajpendo.2000.279.4.E806 11001762 1:CAS:528:DC%2BD3cXnsFOrtLc%3D
PubMed Web of Science ®Google Scholar
BarnesKRKildingAERunning economy: measurement, norms, and determining factorsSports Med - Open20151 8 https://doi.org/10.1186/s40798-015-0007-y 27747844 4555089
PubMedGoogle Scholar
FraynKNCalculation of substrate oxidation rates in vivo from gaseous exchangeJ Appl Physiol198355 628 634 https://doi.org/10.1152/jappl.1983.55.2.628 6618956 1:CAS:528:DyaL3sXltFyrsL0%3D
PubMed Web of Science ®Google Scholar
HoodDAMechanisms of exercise-induced mitochondrial biogenesis in skeletal muscleAppl Physiol Nutr Metab Physiol Appl Nutr Metab200934 465 472 https://doi.org/10.1139/H09-045 1:CAS:528:DC%2BD1MXmtFSnurw%3D
Web of Science ®Google Scholar
RangwalaSMWangXCalvoJALindsleyLZhangYDeynekoG et al Estrogen-related receptor gamma is a key regulator of muscle mitochondrial activity and oxidative capacityJ Biol Chem2010285 22619 22629 https://doi.org/10.1074/jbc.M110.125401 20418374 2903389 1:CAS:528:DC%2BC3cXos1WntLc%3D
PubMed Web of Science ®Google Scholar
LaiRYJLjubicicVD’souzaDHoodDAEffect of chronic contractile activity on mRNA stability in skeletal muscleAm J Physiol - Cell Physiol2010299 C155 C163 https://doi.org/10.1152/ajpcell.00523.2009 20375275 2904257 1:CAS:528:DC%2BC3cXpslSgsLg%3D
PubMedGoogle Scholar
PilegaardHSaltinBNeuferPDExercise induces transient transcriptional activation of the PGC-1alpha gene in human skeletal muscleJ Physiol2003546 Pt 3 851 858 https://doi.org/10.1113/jphysiol.2002.034850 12563009 2342594 1:CAS:528:DC%2BD3sXitlSmtrg%3D
PubMed Web of Science ®Google Scholar
AlaynickWAKondoRPXieWHeWDufourCRDownesM et al ERRγ directs and maintains the transition to oxidative metabolism in the postnatal heartCell Metab20076 13 24 https://doi.org/10.1016/j.cmet.2007.06.007 17618853 1:CAS:528:DC%2BD2sXotlCitLw%3D
PubMed Web of Science ®Google Scholar
LiuDZhangZTengCTEstrogen-related receptor-gamma and peroxisome proliferator-activated receptor-gamma coactivator-1alpha regulate estrogen-related receptor-alpha gene expression via a conserved multi-hormone response elementJ Mol Endocrinol200534 473 487 https://doi.org/10.1677/jme.1.01586 15821111 1:CAS:528:DC%2BD2MXjslGgsr0%3D
PubMedGoogle Scholar
KannistoKChibalinAGlinghammarBZierathJRHamstenAEhrenborgEDifferential expression of peroxisomal proliferator activated receptors α and δ in skeletal muscle in response to changes in diet and exerciseInt J Mol Med200617 45 52 16328010 1:CAS:528:DC%2BD28Xntlajsg%3D%3D
PubMed Web of Science ®Google Scholar
BurkartEMSambandamNHanXGrossRWCourtoisMGieraschCM et al Nuclear receptors PPARβ/δ and PPARα direct distinct metabolic regulatory programs in the mouse heartJ Clin Invest2007117 3930 3939 18037994 2082147 1:CAS:528:DC%2BD2sXhsValsLzM
PubMed Web of Science ®Google Scholar
KleinerSNguyen-TranVBaréOHuangXSpiegelmanBWuZPPAR{delta} agonism activates fatty acid oxidation via PGC-1{alpha} but does not increase mitochondrial gene expression and functionJ Biol Chem2009284 18624 18633 https://doi.org/10.1074/jbc.M109.008797 19435887 2707195 1:CAS:528:DC%2BD1MXotVKns78%3D
PubMed Web of Science ®Google Scholar
TanakaTYamamotoJIwasakiSAsabaHHamuraHIkedaY et al Activation of peroxisome proliferator-activated receptor delta induces fatty acid beta-oxidation in skeletal muscle and attenuates metabolic syndromeProc Natl Acad Sci U S A2003100 15924 15929 https://doi.org/10.1073/pnas.0306981100 14676330 307669 1:CAS:528:DC%2BD2cXhtVCkug%3D%3D
PubMed Web of Science ®Google Scholar
YuanHLuJXiaoJUpadhyayGUmansRKallakuryB et al PPARδ induces estrogen receptor-positive mammary neoplasia through an inflammatory and metabolic phenotype linked to mTOR activationCancer Res201373 4349 4361 https://doi.org/10.1158/0008-5472.CAN-13-0322 23811944 3723355 1:CAS:528:DC%2BC3sXhtFSrtrnO
PubMedGoogle Scholar
McFarlanJTYoshidaYJainSSHanX-XSnookLALallyJ et al In vivo, fatty acid translocase (CD36) critically regulates skeletal muscle fuel selection, exercise performance, and training-induced adaptation of fatty acid oxidationJ Biol Chem2012287 23502 23516 https://doi.org/10.1074/jbc.M111.315358 22584574 3390626 1:CAS:528:DC%2BC38XpvVejt7o%3D
PubMedGoogle Scholar
MuoioDMWayJMTannerCJWinegarDAKliewerSAHoumardJA et al Peroxisome proliferator-activated receptor-α regulates fatty acid utilization in primary human skeletal muscle cellsDiabetes200251 901 909 https://doi.org/10.2337/diabetes.51.4.901 11916905 1:CAS:528:DC%2BD38Xis1Ojtb4%3D
PubMed Web of Science ®Google Scholar
SchoonjansKPeinado-OnsurbeJLefebvreAMHeymanRABriggsMDeebS et al PPARalpha and PPARgamma activators direct a distinct tissue-specific transcriptional response via a PPRE in the lipoprotein lipase geneEMBO J199615 5336 5348 8895578 452277 1:CAS:528:DyaK28XmsVeiu7Y%3D https://doi.org/10.1002/j.1460-2075.1996.tb00918.x
PubMed Web of Science ®Google Scholar
AuclairESatabinPServanEGuezennecCYMetabolic effects of glucose, medium chain triglyceride and long chain triglyceride feeding before prolonged exercise in ratsEur J Appl Physiol198857 126 131 https://doi.org/10.1007/BF00691251 1:CAS:528:DyaL1cXht12ht7s%3D
Web of Science ®Google Scholar
PinckaersPJMChurchward-VenneTABaileyDvan LoonLJCKetone bodies and exercise performance: the next magic bullet or merely hype?Sports Med Auckl Nz201747 383 391 https://doi.org/10.1007/s40279-016-0577-y
Web of Science ®Google Scholar
SaitohSShimomuraYSuzukiMEffect of a high-carbohydrate diet intake on muscle glycogen repletion after exercise in rats previously fed a high-fat dietEur J Appl Physiol199366 127 133 https://doi.org/10.1007/BF01427053 1:STN:280:DyaK3s3jtFWgtA%3D%3D
Web of Science ®Google Scholar
SatabinPBois-JoyeuxBChanezMGuezennecCYPeretJEffects of long-term feeding of high-protein or high-fat diets on the response to exercise in the ratEur J Appl Physiol198958 583 590 https://doi.org/10.1007/BF00418503 1:STN:280:DyaL1M3ns1ehsw%3D%3D
Web of Science ®Google Scholar
MaizelsEZRudermanNBGoodmanMNLauDEffect of acetoacetate on glucose metabolism in the soleus and extensor digitorum longus muscles of the ratBiochem J1977162 557 568 https://doi.org/10.1042/bj1620557 869905 1164638 1:CAS:528:DyaE2sXkvVWrsb8%3D
PubMedGoogle Scholar
KuoCHBrowningKSIvyJLRegulation of GLUT4 protein expression and glycogen storage after prolonged exerciseActa Physiol Scand1999165 193 201 https://doi.org/10.1046/j.1365-201x.1999.00489.x 10090331 1:CAS:528:DyaK1MXhsFektrw%3D
PubMedGoogle Scholar
RenJMSemenkovichCFGulveEAGaoJHolloszyJOExercise induces rapid increases in GLUT4 expression, glucose transport capacity, and insulin-stimulated glycogen storage in muscleJ Biol Chem1994269 14396 14401 8182045 1:CAS:528:DyaK2cXjtFKgsLk%3D
PubMed Web of Science ®Google Scholar
RyderJWKawanoYGaluskaDFahlmanRWallberg-HenrikssonHCharronMJ et al Postexercise glucose uptake and glycogen synthesis in skeletal muscle from GLUT4-deficient miceFASEB J Off Publ Fed Am Soc Exp Biol199913 2246 2256 1:CAS:528:DyaK1MXotVKitbw%3D
PubMed Web of Science ®Google Scholar
KerlyMOttawayJHThe effect of diet on glycogen formation in rat liverJ Physiol1954123 516 533 https://doi.org/10.1113/jphysiol.1954.sp005068 13152696 1366223 1:CAS:528:DyaG2cXks12gsw%3D%3D
PubMed Web of Science ®Google Scholar
SanbarSSHetenyiGForbathNEvansJREffects of infusion of octanoate on glucose concentration in plasma and the rates of glucose production and utilization in dogsMetabolism196514 1311 1323 https://doi.org/10.1016/S0026-0495(65)80013-0 5321048 1:CAS:528:DyaF28XjtVeitg%3D%3D
PubMedGoogle Scholar
BaldwinKMReitmanJSTerjungRLWinderWWHolloszyJOSubstrate depletion in different types of muscle and in liver during prolonged runningAm J Phys1973225 1045 1050 1:CAS:528:DyaE2cXisFahug%3D%3D
PubMed Web of Science ®Google Scholar
PedersonBASchroederJMParkerGESmithMWDePaoli-RoachAARoachPJGlucose metabolism in mice lacking muscle glycogen synthaseDiabetes200554 3466 3473 https://doi.org/10.2337/diabetes.54.12.3466 16306363 1:CAS:528:DC%2BD2MXht12gsL7N
PubMed Web of Science ®Google Scholar
GoodmanMNBergerMRudermanNBGlucose metabolism in rat skeletal muscle at rest: effect of starvation, diabetes, ketone bodies and free fatty acidsDiabetes197423 881 888 https://doi.org/10.2337/diab.23.11.881 4279193 1:CAS:528:DyaE2MXlsVyluw%3D%3D
PubMedGoogle Scholar
HicksonRCRennieMJConleeRKWinderWWHolloszyJOEffects of increased plasma fatty acids on glycogen utilization and enduranceJ Appl Physiol197743 829 833 https://doi.org/10.1152/jappl.1977.43.5.829 591476 1:CAS:528:DyaE1cXhvFKguw%3D%3D
PubMed Web of Science ®Google Scholar
RennieMJWinderWWHolloszyJOA sparing effect of increased plasma fatty acids on muscle and liver glycogen content in the exercising ratBiochem J1976156 647 655 https://doi.org/10.1042/bj1560647 949346 1163799 1:CAS:528:DyaE28Xlt1ShtrY%3D
PubMed Web of Science ®Google Scholar
RudermanNBHoughtonCRSHemsREvaluation of the isolated perfused rat hindquarter for the study of muscle metabolismBiochem J1971124 639 651 https://doi.org/10.1042/bj1240639 5135248 1177234 1:CAS:528:DyaE3MXltlygu7o%3D
PubMedGoogle Scholar
DoegeHBaillieRAOrtegonAMTsangBWuQPunreddyS et al Targeted deletion of FATP5 reveals multiple functions in liver metabolism: alterations in hepatic lipid homeostasisGastroenterology2006130 1245 1258 https://doi.org/10.1053/j.gastro.2006.02.006 16618416 1:CAS:528:DC%2BD28XksFWmu7s%3D
PubMed Web of Science ®Google Scholar
FrostSCWellsMAA comparison of the utilization of medium and long-chain fatty acids for oxidation and ketogenesis in the suckling rat: in vivo and in vitro studiesArch Biochem Biophys1981211 537 546 https://doi.org/10.1016/0003-9861(81)90488-4 7305388 1:CAS:528:DyaL3MXlsVOru7c%3D
PubMedGoogle Scholar
SmithBKJainSSRimbaudSDamAQuadrilateroJVentura-ClapierR et al FAT/CD36 is located on the outer mitochondrial membrane, upstream of long-chain acyl-CoA synthetase, and regulates palmitate oxidationBiochem J2011437 125 134 https://doi.org/10.1042/BJ20101861 21463259 1:CAS:528:DC%2BC3MXnsVCjtrs%3D
PubMedGoogle Scholar
ZammitVAThe effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-l-carnitine and octanoate by isolated liver mitochondriaBiochem J1980190 293 300 https://doi.org/10.1042/bj1900293 7470052 1162093 1:CAS:528:DyaL3cXmtlGrtLc%3D
PubMedGoogle Scholar
MannaertsGPThomasJDebeerLJMcGarryJDFosterDWHepatic fatty acid oxidation and ketogenesis after clofibrate treatmentBiochim Biophys Acta BBA - Lipids Lipid Metab1978529 201 211 https://doi.org/10.1016/0005-2760(78)90063-2 1:CAS:528:DyaE1cXlt1eju7c%3D
Web of Science ®Google Scholar
LhuilleryCMebarkiSLecourtierMJDemarneYInfluence of different dietary fats on the incorporation of exogenous fatty acids into rat adipose glyceridesJ Nutr1988118 1447 1454 https://doi.org/10.1093/jn/118.12.1447 3210074 1:CAS:528:DyaL1MXhtFemtL4%3D
PubMedGoogle Scholar
MaragoudakisMEKalinskyHJLennaneJMetabolism of octanoate and its effect on glucose and palmitate utilization by isolated fat cellsProc Soc Exp Biol Med Soc Exp Biol Med N Y N1975148 606 610 https://doi.org/10.3181/00379727-148-38593 1:CAS:528:DyaE2MXhs1yjs7o%3D
Web of Science ®Google Scholar
ScheigRKlatskinGHepatic metabolism of 1-14C octanoic and 1-14C palmitic acidsJ Am Oil Chem Soc196845 31 33 https://doi.org/10.1007/BF02679042 5642083 1:CAS:528:DyaF1cXkslKktA%3D%3D
PubMed Web of Science ®Google Scholar
Vilà-BrauASousa-CoelhoALDMayordomoCHaroDMarreroPFHuman HMGCS2 regulates mitochondrial fatty acid oxidation and FGF21 expression in HepG2 cell lineJ Biol Chem2011286 20423 20430 https://doi.org/10.1074/jbc.M111.235044 21502324 3121469 1:CAS:528:DC%2BC3MXmvFCgt78%3D
PubMed Web of Science ®Google Scholar
BrounsFvan der VusseGJUtilization of lipids during exercise in human subjects: metabolic and dietary constraintsBr J Nutr199879 117 128 https://doi.org/10.1079/BJN19980022 9536855 1:CAS:528:DyaK1cXislyms7c%3D
PubMedGoogle Scholar

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Low-fat diet, and medium-fat diets containing coconut oil and soybean oil exert different metabolic effects in untrained and treadmill-trained mice

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Low-fat diet, and medium-fat diets containing coconut oil and soybean oil exert different metabolic effects in untrained and treadmill-trained mice

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