Upregulated hepatic lipogenesis from dietary sugars in response to low palmitate feeding supplies brain palmitate.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
17 Jan 2024
Historique:
received: 06 03 2023
accepted: 12 12 2023
medline: 18 1 2024
pubmed: 18 1 2024
entrez: 17 1 2024
Statut: epublish

Résumé

Palmitic acid (PAM) can be provided in the diet or synthesized via de novo lipogenesis (DNL), primarily, from glucose. Preclinical work on the origin of brain PAM during development is scarce and contrasts results in adults. In this work, we use naturally occurring carbon isotope ratios (

Identifiants

pubmed: 38233416
doi: 10.1038/s41467-023-44388-4
pii: 10.1038/s41467-023-44388-4
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

490

Subventions

Organisme : Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada)
ID : RGPIN-2017-06465

Informations de copyright

© 2024. The Author(s).

Références

Clandinin, M. T. et al. Intrauterine fatty acid accretion rates in human brain: implications for fatty acid requirements. Early Hum. Dev. 4, 121–129 (1980).
pubmed: 7408742 doi: 10.1016/0378-3782(80)90015-8
Clandinin, M. T. et al. Extrauterine fatty acid accretion in infant brain: implications for fatty acid requirements. Early Hum. Dev. 4, 131–138 (1980).
pubmed: 7408743 doi: 10.1016/0378-3782(80)90016-X
Lacombe, R. J. S. et al. Quantitative and carbon isotope ratio analysis of fatty acids isolated from human brain hemispheres. J. Neurochem. https://doi.org/10.1111/jnc.15702 (2022).
Martinez, M. Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders. Brain Res. 583, 171–182 (1992).
pubmed: 1504825 doi: 10.1016/S0006-8993(10)80021-6
Carta, G., Murru, E., Banni, S. & Manca, C. Palmitic acid: physiological role, metabolism and nutritional implications. Front. Physiol. 8, 902 (2017).
pubmed: 29167646 pmcid: 5682332 doi: 10.3389/fphys.2017.00902
Innis, S. M. Palmitic acid in early human development. Crit. Rev. Food Sci. Nutr. 56, 1952–1959 (2016).
pubmed: 25764297 doi: 10.1080/10408398.2015.1018045
Innis, S. M. Dietary triacylglycerol structure and its role in infant nutrition. Adv. Nutr. 2, 275–283 (2011).
pubmed: 22332059 pmcid: 3090172 doi: 10.3945/an.111.000448
Smith, M. E., Cisbani, G., Lacombe, R. J. S. & Bazinet, R. P. A scoping review of clinical studies in infants fed formulas containing palm oil or palm olein and Sn-2 palmitate. J. Nutr. 151, 2997–3035 (2021).
pubmed: 34510181 pmcid: 8485903 doi: 10.1093/jn/nxab246
Edmond, J., Higa, T. A., Korsak, R. A., Bergner, E. A. & Lee, W. N. Fatty acid transport and utilization for the developing brain. J. Neurochem. 70, 1227–1234 (1998).
pubmed: 9489745 doi: 10.1046/j.1471-4159.1998.70031227.x
Marbois, B. N., Ajie, H. O., Korsak, R. A., Sensharma, D. K. & Edmond, J. The origin of palmitic acid in brain of the developing rat. Lipids 27, 587–592 (1992).
pubmed: 1406069 doi: 10.1007/BF02536115
Chen, C. T. et al. The low levels of eicosapentaenoic acid in rat brain phospholipids are maintained via multiple redundant mechanisms. J. Lipid Res. 54, 2410–2422 (2013).
pubmed: 23836105 pmcid: 3735939 doi: 10.1194/jlr.M038505
Dhopeshwarkar, G. A., Subramanian, C., McConnell, D. H. & Mead, J. F. Fatty acid transport into the brain. Biochim. Biophys. Acta 255, 572–579 (1972).
pubmed: 5057935 doi: 10.1016/0005-2736(72)90161-7
Dhopeshwarkar, G. A. & Mead, J. F. Fatty acid uptake by the brain: II. Incorporation of [1-14C] palmitic acid into the adult rat brain. Biochim. Biophys. Acta BBA Lipids Lipid Metab. 187, 461–467 (1969).
doi: 10.1016/0005-2760(69)90042-3
Golovko, M. Y. et al. Synuclein gene deletion decreases brain palmitate uptake and alters the palmitate metabolism in the absence of α-synuclein palmitate binding. Biochemistry 44, 8251–8259 (2005).
pubmed: 15938614 doi: 10.1021/bi0502137
Kimes, A. S., Sweeney, D., London, E. D. & Rapoport, S. I. Palmitate incorporation into different brain regions in the awake rat. Brain Res. 274, 291–301 (1983).
pubmed: 6626956 doi: 10.1016/0006-8993(83)90707-2
Smith, Q. R. & Nagura, H. Fatty acid uptake and incorporation in brain: studies with the perfusion model. J. Mol. Neurosci. 16, 167–172 (2001).
pubmed: 11478371 doi: 10.1385/JMN:16:2-3:167
Lacombe, R. J. S. & Bazinet, R. P. Natural abundance carbon isotope ratio analysis and its application in the study of diet and metabolism. Nutr. Rev. 79, 869–888 (2021).
pubmed: 33141222 doi: 10.1093/nutrit/nuaa109
Smith, M. E., Cisbani, G., Metherel, A. H. & Bazinet, R. P. The majority of brain palmitic acid is maintained by lipogenesis from dietary sugars and is augmented in mice fed low palmitic acid levels from birth. J. Neurochem. 161, 112–128 (2022).
pubmed: 34780089 doi: 10.1111/jnc.15539
Bergen, W. G. & Mersmann, H. J. Comparative aspects of lipid metabolism: impact on contemporary research and use of animal models. J. Nutr. 135, 2499–2502 (2005).
pubmed: 16251600 doi: 10.1093/jn/135.11.2499
Lacombe, R. J. S., Giuliano, V., Chouinard-Watkins, R. & Bazinet, R. P. Natural abundance carbon isotopic analysis indicates the equal contribution of local synthesis and plasma uptake to palmitate levels in the mouse brain. Lipids 53, 481–490 (2018).
pubmed: 29923600 doi: 10.1002/lipd.12046
Chen, C. T., Ma, D. W. L., Kim, J. H., Mount, H. T. J. & Bazinet, R. P. The low density lipoprotein receptor is not necessary for maintaining mouse brain polyunsaturated fatty acid concentrations. J. Lipid Res. 49, 147–152 (2008).
pubmed: 17932396 doi: 10.1194/jlr.M700386-JLR200
Fu, X. et al. Measurement of lipogenic flux by deuterium resolved mass spectrometry. Nat. Commun. 12, 3756 (2021).
pubmed: 34145255 pmcid: 8213799 doi: 10.1038/s41467-021-23958-4
Horton, J. D., Goldstein, J. L. & Brown, M. S. SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver. J. Clin. Investig. 109, 1125–1131 (2002).
pubmed: 11994399 pmcid: 150968 doi: 10.1172/JCI0215593
Ortega-Prieto, P. & Postic, C. Carbohydrate sensing through the transcription factor ChREBP. Front. Genet. 10, 472 (2019).
pubmed: 31275349 pmcid: 6593282 doi: 10.3389/fgene.2019.00472
Jones, J. G. Identifying sources of hepatic lipogenic acetyl-CoA using stable isotope tracers and NMR. Adv. Radiol. 2014, e109252 (2014).
doi: 10.1155/2014/109252
Cunnane, S. C. et al. Brain energy rescue: an emerging therapeutic concept for neurodegenerative disorders of ageing. Nat. Rev. Drug Discov. 19, 609–633 (2020).
pubmed: 32709961 pmcid: 7948516 doi: 10.1038/s41573-020-0072-x
Cunnane, S. C. & Crawford, M. A. Energetic and nutritional constraints on infant brain development: Implications for brain expansion during human evolution. J. Hum. Evol. 77, 88–98 (2014).
pubmed: 24928072 doi: 10.1016/j.jhevol.2014.05.001
Edmond, J. Ketone bodies as precursors of sterols and fatty acids in the developing rat. J. Biol. Chem. 249, 72–80 (1974).
pubmed: 4809632 doi: 10.1016/S0021-9258(19)43092-5
Menard, C. R., Goodman, K. J., Corso, T. N., Brenna, J. T. & Cunnane, S. C. Recycling of carbon into lipids synthesized de novo is a quantitatively important pathway of alpha-[U-13C]linolenate utilization in the developing rat brain. J. Neurochem. 71, 2151–2158 (1998).
Igarashi, M. et al. Upregulated liver conversion of alpha-linolenic acid to docosahexaenoic acid in rats on a 15 week n-3 PUFA-deficient diet. J. Lipid Res. 48, 152–164 (2007).
pubmed: 17050905 doi: 10.1194/jlr.M600396-JLR200
Igarashi, M. et al. Docosahexaenoic acid synthesis from alpha-linolenic acid by rat brain is unaffected by dietary n-3 PUFA deprivation. J. Lipid Res. 48, 1150–1158 (2007).
pubmed: 17277380 doi: 10.1194/jlr.M600549-JLR200
Igarashi, M., Ma, K., Chang, L., Bell, J. M. & Rapoport, S. I. Dietary n-3 PUFA deprivation for 15 weeks upregulates elongase and desaturase expression in rat liver but not brain. J. Lipid Res. 48, 2463–2470 (2007).
pubmed: 17715424 doi: 10.1194/jlr.M700315-JLR200
Han, L.-Q. et al. [mRNA expression of lipogenic genes in mouse mammary gland in different lactation stages]. Yi Chuan Hered. 34, 335–341 (2012).
doi: 10.3724/SP.J.1005.2012.00335
Rudolph, M. C., McManaman, J. L., Hunter, L., Phang, T. & Neville, M. C. Functional development of the mammary gland: use of expression profiling and trajectory clustering to reveal changes in gene expression during pregnancy, lactation, and involution. J. Mammary Gland Biol. Neoplasia 8, 287–307 (2003).
pubmed: 14973374 doi: 10.1023/B:JOMG.0000010030.73983.57
Rudolph, M. C. et al. Metabolic regulation in the lactating mammary gland: a lipid synthesizing machine. Physiol. Genomics 28, 323–336 (2007).
pubmed: 17105756 doi: 10.1152/physiolgenomics.00020.2006
Rudolph, M. C. et al. Sterol regulatory element binding protein and dietary lipid regulation of fatty acid synthesis in the mammary epithelium. Am. J. Physiol. Endocrinol. Metab. 299, E918–927 (2010).
pubmed: 20739508 pmcid: 3006251 doi: 10.1152/ajpendo.00376.2010
Smith, S., Gagné, H. T., Pitelka, D. R. & Abraham, S. The effect of dietary fat on lipogenesis in mammary gland and liver from lactating and virgin mice. Biochem. J. 115, 807–815 (1969).
pubmed: 5390535 pmcid: 1185209 doi: 10.1042/bj1150807
Kaur, B., Jørgensen, A. & Duttaroy, A. K. Fatty acid uptake by breast cancer cells (MDA-MB-231): Effects of insulin, leptin, adiponectin, and TNFα. Prostaglandins Leukot. Essent. Fat. Acids 80, 93–99 (2009).
doi: 10.1016/j.plefa.2009.01.002
Menendez, J. A. et al. Overexpression and hyperactivity of breast cancer-associated fatty acid synthase (oncogenic antigen-519) is insensitive to normal arachidonic fatty acid-induced suppression in lipogenic tissues but it is selectively inhibited by tumoricidal alpha-linolenic and gamma-linolenic fatty acids: a novel mechanism by which dietary fat can alter mammary tumorigenesis. Int. J. Oncol. 24, 1369–1383 (2004).
pubmed: 15138577
Menendez, J. A., Colomer, R. & Lupu, R. Why does tumor-associated fatty acid synthase (oncogenic antigen-519) ignore dietary fatty acids? Med. Hypotheses 64, 342–349 (2005).
pubmed: 15607569 doi: 10.1016/j.mehy.2004.07.022
Hopperton, K. E., Duncan, R. E., Bazinet, R. P. & Archer, M. C. Fatty acid synthase plays a role in cancer metabolism beyond providing fatty acids for phospholipid synthesis or sustaining elevations in glycolytic activity. Exp. Cell Res. 320, 302–310 (2014).
pubmed: 24200503 doi: 10.1016/j.yexcr.2013.10.016
Funai, K. et al. Muscle lipogenesis balances insulin sensitivity and strength through calcium signaling. J. Clin. Investig. 123, 1229–1240 (2013).
pubmed: 23376793 pmcid: 3582136 doi: 10.1172/JCI65726
Rowland, L. A. et al. De novo lipogenesis fuels adipocyte autophagosome and lysosome membrane dynamics. Nat. Commun. 14, 1362 (2023).
Rajagopal, R. et al. Retinal de novo lipogenesis coordinates neurotrophic signaling to maintain vision. JCI Insight 3, e97076 (2018).
Montani, L. et al. De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination. J. Cell Biol. 217, 1353–1368 (2018).
pubmed: 29434029 pmcid: 5881495 doi: 10.1083/jcb.201706010
Murphy, E. J. Glucose as a carbon source to synthesize palmitate de novo in the adult rodent brain: Adding to the carbon recycling story in the brain. J. Neurochem. 161, 109–111 (2022).
pubmed: 35224738 doi: 10.1111/jnc.15592
Chen, C. T. et al. Inhibiting mitochondrial β-oxidation selectively reduces levels of nonenzymatic oxidative polyunsaturated fatty acid metabolites in the brain. J. Cereb. Blood Flow. Metab. 34, 376–379 (2014).
pubmed: 24326387 doi: 10.1038/jcbfm.2013.221
Brose, S. A., Marquardt, A. L. & Golovko, M. Y. Fatty acid biosynthesis from glutamate and glutamine is specifically induced in neuronal cells under hypoxia. J. Neurochem. 129, 400–412 (2014).
pubmed: 24266789 doi: 10.1111/jnc.12617
Brose, S. A., Golovko, S. A. & Golovko, M. Y. Fatty acid biosynthesis inhibition increases reduction potential in neuronal cells under hypoxia. Front. Neurosci. 10, 546 (2016).
pubmed: 27965531 pmcid: 5127813 doi: 10.3389/fnins.2016.00546
Han, X. & Simon, M. C. NAD+ regeneration drives cancer cell proliferation. Nat. Metab. 4, 647–648 (2022).
pubmed: 35739398 doi: 10.1038/s42255-022-00586-w
Giuliano, V., Lacombe, R. J. S., Hopperton, K. E. & Bazinet, R. P. Applying stable carbon isotopic analysis at the natural abundance level to determine the origin of docosahexaenoic acid in the brain of the fat-1 mouse. Biochim. Biophys. Acta Mol. Cell Biol. Lipids 1863, 1388–1398 (2018).
pubmed: 30075211 doi: 10.1016/j.bbalip.2018.07.014
Hopperton, K. E., Trépanier, M.-O., Giuliano, V. & Bazinet, R. P. Brain omega-3 polyunsaturated fatty acids modulate microglia cell number and morphology in response to intracerebroventricular amyloid-β 1-40 in mice. J. Neuroinflammation 13, 257 (2016).
pubmed: 27688126 pmcid: 5041295 doi: 10.1186/s12974-016-0721-5
Folch, J., Lees, M. & Sloane Stanley, G. H. A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 226, 497–509 (1957).
pubmed: 13428781 doi: 10.1016/S0021-9258(18)64849-5
Coplen, T. B. Discontinuance of SMOW and PDB. Nature 375, 285–285 (1995).
doi: 10.1038/375285a0
Coplen, T. B. et al. New guidelines for delta13C measurements. Anal. Chem. 78, 2439–2441 (2006).
pubmed: 16579631 doi: 10.1021/ac052027c
Hoffman, D. W. & Rasmussen, C. Absolute carbon stable isotope ratio in the vienna peedee belemnite isotope reference determined by 1H NMR spectroscopy. Anal. Chem. 94, 5240–5247 (2022).
pubmed: 35312289 doi: 10.1021/acs.analchem.1c04565
Schimmelmann, A. et al. Organic reference materials for hydrogen, carbon, and nitrogen stable isotope-ratio measurements: caffeines, n-alkanes, fatty acid methyl esters, glycines, l-valines, polyethylenes, and oils. Anal. Chem. 88, 4294–4302 (2016).
pubmed: 26974360 doi: 10.1021/acs.analchem.5b04392
Brenna, J. T., Corso, T. N., Tobias, H. J. & Caimi, R. J. High-precision continuous-flow isotope ratio mass spectrometry. Mass Spectrom. Rev. 16, 227–258 (1997).
pubmed: 9538528 doi: 10.1002/(SICI)1098-2787(1997)16:5<227::AID-MAS1>3.0.CO;2-J
McKINNEY, C. R., McCREA, J. M., Epstein, S., Allen, H. A. & Urey, H. C. Improvements in mass spectrometers for the measurement of small differences in isotope abundance ratios. Rev. Sci. Instrum. 21, 724–730 (1950).
pubmed: 14781446 doi: 10.1063/1.1745698
Lacombe, R. J. S., Giuliano, V., Colombo, S. M., Arts, M. T. & Bazinet, R. P. Compound-specific isotope analysis resolves the dietary origin of docosahexaenoic acid in the mouse brain. J. Lipid Res. 58, 2071–2081 (2017).
pubmed: 28694298 pmcid: 5625118 doi: 10.1194/jlr.D077990
Ge, S. X., Son, E. W. & Yao, R. iDEP: an integrated web application for differential expression and pathway analysis of RNA-Seq data. BMC Bioinform. 19, 534 (2018).
doi: 10.1186/s12859-018-2486-6
Ge, X. iDEP web application for RNA-Seq data analysis. Methods Mol. Biol. 2284, 417–443 (2021).
pubmed: 33835455 doi: 10.1007/978-1-0716-1307-8_22
Korotkevich, G. et al. Fast gene set enrichment analysis. Preprint at https://www.biorxiv.org/content/10.1101/060012v3 (2021).
Hess, S. E. et al. Home Improvement: C57BL/6J Mice Given More Naturalistic Nesting Materials Build Better Nests. J. Am. Assoc. Lab. Anim. Sci. 47, 25–31 (2008).
pubmed: 19049249 pmcid: 2687128
Arsenault, D., St-Amour, I., Cisbani, G., Rousseau, L.-S. & Cicchetti, F. The different effects of LPS and poly I:C prenatal immune challenges on the behavior, development and inflammatory responses in pregnant mice and their offspring. Brain. Behav. Immun. 38, 77–90 (2014).
pubmed: 24384468 doi: 10.1016/j.bbi.2013.12.016
Heyser, C. J. Assessment of developmental milestones in rodents. Curr. Protoc. Neurosci. 25, 8.18.1–8.18.15 (2003).

Auteurs

Mackenzie E Smith (ME)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Chuck T Chen (CT)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Chiraag A Gohel (CA)

Department of Biostatistics and Bioinformatics, George Washington University, 950 New Hampshire Ave, NW, Washington, DC, 20052, USA.

Giulia Cisbani (G)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Daniel K Chen (DK)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Kimia Rezaei (K)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Andrew McCutcheon (A)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada.

Richard P Bazinet (RP)

Department of Nutritional Sciences, University of Toronto, 1 King's College Circle, Toronto, M5S 1A8, ON, Canada. richard.bazinet@utoronto.ca.

Classifications MeSH