Lipolysis pathways modulate lipid mediator release and endocannabinoid system signaling in dairy cows' adipocytes.

Adipose tissue Dairy cows Endocannabinoid system Endocannabinoids Lipolysis

Journal

Journal of animal science and biotechnology
ISSN: 1674-9782
Titre abrégé: J Anim Sci Biotechnol
Pays: England
ID NLM: 101581293

Informations de publication

Date de publication:
03 Aug 2024
Historique:
received: 22 03 2024
accepted: 11 06 2024
medline: 3 8 2024
pubmed: 3 8 2024
entrez: 2 8 2024
Statut: epublish

Résumé

As cows transition from pregnancy to lactation, free fatty acids (FFA) are mobilized from adipose tissues (AT) through lipolysis to counter energy deficits. In clinically healthy cows, lipolysis intensity is reduced throughout lactation; however, if FFA release exceeds tissue demands or the liver's metabolic capacity, lipid byproducts accumulate, increasing cows' risk of metabolic and infectious disease. Endocannabinoids (eCBs) and their congeners, N-acylethanolamines (NAEs), are lipid-based compounds that modulate metabolism and inflammation. Their synthesis and release depend upon the availability of FFA precursors and the abundance of synthesizing and degrading enzymes and transporters. Therefore, we hypothesized that eCB production and transcription of endocannabinoid system components are modulated by lipolysis pathways in adipocytes. To test this hypothesis, we stimulated canonical (isoproterenol, 1 µmol/L; ISO) and inflammatory (lipopolysaccharide, 1 µg/mL; LPS) lipolysis pathways in adipocytes isolated from the AT of 5 Holstein dairy cows. Following, we assessed lipolysis intensity, adipocytes' release of eCBs, and transcription of endocannabinoid system components. We found that ISO and LPS stimulated lipolysis at comparable intensities. Exposure to either treatment tended to elevate the release of eCBs and NAEs by cultured adipocytes; however, specific eCBs and NAEs and the transcriptional profiles differed by treatment. On one hand, ISO enhanced adipocytes' release of 2-arachidonoylglycerol (2-AG) but reduced NAE production. Notably, ISO enhanced the cells' expression of enzymes associated with 2-AG biosynthesis (INPP5F, GDPD5, GPAT4), transport (CD36), and adipogenesis (PPARG). Conversely, LPS enhanced adipocytes' synthesis and release of N-arachidonoylethanolamide (AEA). This change coincided with enhanced transcription of the NAE-biosynthesizing enzyme, PTPN22, and adipocytes' transcription of genes related to eCB degradation (PTGS2, MGLL, CYP27B1). Furthermore, LPS enhanced adipocytes' transcription of eCB and NAE transporters (HSPA1A, SCP2) and the expression of the anti-adipogenic ion channel, TRPV3. Our data provide evidence for distinct modulatory roles of canonical and inflammatory lipolysis pathways over eCB release and transcriptional regulation of biosynthesis, degradation, transport, and ECS signaling in cows' adipocytes. Based on our findings, we conclude that, within adipocytes, eCB production and ECS component expression are, at least in part, mediated by lipolysis in a pathway-dependent manner. These findings contribute to a deeper understanding of the molecular mechanisms underlying metabolic regulation in dairy cows' AT, with potential implications for prevention and treatment of inflammatory and metabolic disorders.

Sections du résumé

BACKGROUND BACKGROUND
As cows transition from pregnancy to lactation, free fatty acids (FFA) are mobilized from adipose tissues (AT) through lipolysis to counter energy deficits. In clinically healthy cows, lipolysis intensity is reduced throughout lactation; however, if FFA release exceeds tissue demands or the liver's metabolic capacity, lipid byproducts accumulate, increasing cows' risk of metabolic and infectious disease. Endocannabinoids (eCBs) and their congeners, N-acylethanolamines (NAEs), are lipid-based compounds that modulate metabolism and inflammation. Their synthesis and release depend upon the availability of FFA precursors and the abundance of synthesizing and degrading enzymes and transporters. Therefore, we hypothesized that eCB production and transcription of endocannabinoid system components are modulated by lipolysis pathways in adipocytes. To test this hypothesis, we stimulated canonical (isoproterenol, 1 µmol/L; ISO) and inflammatory (lipopolysaccharide, 1 µg/mL; LPS) lipolysis pathways in adipocytes isolated from the AT of 5 Holstein dairy cows. Following, we assessed lipolysis intensity, adipocytes' release of eCBs, and transcription of endocannabinoid system components.
RESULTS RESULTS
We found that ISO and LPS stimulated lipolysis at comparable intensities. Exposure to either treatment tended to elevate the release of eCBs and NAEs by cultured adipocytes; however, specific eCBs and NAEs and the transcriptional profiles differed by treatment. On one hand, ISO enhanced adipocytes' release of 2-arachidonoylglycerol (2-AG) but reduced NAE production. Notably, ISO enhanced the cells' expression of enzymes associated with 2-AG biosynthesis (INPP5F, GDPD5, GPAT4), transport (CD36), and adipogenesis (PPARG). Conversely, LPS enhanced adipocytes' synthesis and release of N-arachidonoylethanolamide (AEA). This change coincided with enhanced transcription of the NAE-biosynthesizing enzyme, PTPN22, and adipocytes' transcription of genes related to eCB degradation (PTGS2, MGLL, CYP27B1). Furthermore, LPS enhanced adipocytes' transcription of eCB and NAE transporters (HSPA1A, SCP2) and the expression of the anti-adipogenic ion channel, TRPV3.
CONCLUSIONS CONCLUSIONS
Our data provide evidence for distinct modulatory roles of canonical and inflammatory lipolysis pathways over eCB release and transcriptional regulation of biosynthesis, degradation, transport, and ECS signaling in cows' adipocytes. Based on our findings, we conclude that, within adipocytes, eCB production and ECS component expression are, at least in part, mediated by lipolysis in a pathway-dependent manner. These findings contribute to a deeper understanding of the molecular mechanisms underlying metabolic regulation in dairy cows' AT, with potential implications for prevention and treatment of inflammatory and metabolic disorders.

Identifiants

pubmed: 39095900
doi: 10.1186/s40104-024-01062-z
pii: 10.1186/s40104-024-01062-z
doi:

Types de publication

Journal Article

Langues

eng

Pagination

103

Subventions

Organisme : Michigan Alliance for Animal Agriculture
ID : AA-23-0014
Organisme : National Institute of Food and Agriculture
ID : 2019-67015-29443
Organisme : National Institute of Food and Agriculture
ID : 2021-67037-34657
Organisme : National Institute of Food and Agriculture
ID : 2023-11488
Organisme : United States - Israel Binational Agricultural Research and Development Fund
ID : IS-5167-19

Informations de copyright

© 2024. The Author(s).

Références

LeBlanc S. Monitoring metabolic health of dairy cattle in the transition period. J Reprod Dev. 2010;56(Suppl):S29–35.
pubmed: 20629214 doi: 10.1262/jrd.1056S29
Contreras GA, Sordillo LM. Lipid mobilization and inflammatory responses during the transition period of dairy cows. Comp Immunol Microbiol Infect Dis. 2011;34(3):281–9.
pubmed: 21316109 doi: 10.1016/j.cimid.2011.01.004
Contreras GA, Strieder-Barboza C, Raphael W. Adipose tissue lipolysis and remodeling during the transition period of dairy cows. J Anim Sci Biotechnol. 2017;8:41.
pubmed: 28484594 pmcid: 5420123 doi: 10.1186/s40104-017-0174-4
Grabner GF, Xie H, Schweiger M, Zechner R. Lipolysis: cellular mechanisms for lipid mobilization from fat stores. Nat Metab. 2021;3(11):1445–65.
pubmed: 34799702 doi: 10.1038/s42255-021-00493-6
Granneman JG, Moore HP, Granneman RL, Greenberg AS, Obin MS, Zhu Z. Analysis of lipolytic protein trafficking and interactions in adipocytes. J Biol Chem. 2007;282(8):5726–35.
pubmed: 17189257 doi: 10.1074/jbc.M610580200
Granneman JG, Moore HP, Krishnamoorthy R, Rathod M. Perilipin controls lipolysis by regulating the interactions of AB-hydrolase containing 5 (Abhd5) and adipose triglyceride lipase (Atgl). J Biol Chem. 2009;284(50):34538–44.
pubmed: 19850935 pmcid: 2787315 doi: 10.1074/jbc.M109.068478
Ospina PA, McArt JA, Overton TR, Stokol T, Nydam DV. Using nonesterified fatty acids and β-hydroxybutyrate concentrations during the transition period for herd-level monitoring of increased risk of disease and decreased reproductive and milking performance. Vet Clin North Am Food Anim Pract. 2013;29(2):387–412.
pubmed: 23809897 doi: 10.1016/j.cvfa.2013.04.003
Contreras GA, Strieder-Barboza C, de Souza J, Gandy J, Mavangira V, Lock AL, et al. Periparturient lipolysis and oxylipid biosynthesis in bovine adipose tissues. PLoS One. 2017;12(12):e0188621.
pubmed: 29206843 pmcid: 5716552 doi: 10.1371/journal.pone.0188621
Contreras GA, O’Boyle NJ, Herdt TH, Sordillo LM. Lipomobilization in periparturient dairy cows influences the composition of plasma nonesterified fatty acids and leukocyte phospholipid fatty acids. J Dairy Sci. 2010;93(6):2508–16.
pubmed: 20494158 doi: 10.3168/jds.2009-2876
Eckel EF, Ametaj BN. Invited Review: Bacterial endotoxins in the etiopathogenesis of periparturient diseases of transition dairy cows. J Dairy Sci. 2016;99(8):5967–90.
Chirivi M, Rendon CJ, Myers MN, Prom CM, Roy S, Sen A, et al. Lipopolysaccharide induces lipolysis and insulin resistance in adipose tissue from dairy cows. J Dairy Sci. 2022;105(1):842–55.
pubmed: 34696909 doi: 10.3168/jds.2021-20855
Chirivi M, Contreras GA. Endotoxin activates lipolysis through TLR4 signaling in bovine adipocytes. J Dairy Sci. 2022;105(Suppl. 1):336. (Abstr.)
Myers MN, Zachut M, Tam J, Contreras GA. A proposed modulatory role of the endocannabinoid system on adipose tissue metabolism and appetite in periparturient dairy cows. J Anim Sci Biotechnol. 2021;12:21.
pubmed: 33663611 pmcid: 7934391 doi: 10.1186/s40104-021-00549-3
Bonsale R, Seyed Sharifi R, Dirandeh E, Hedayat N, Mojtahedin A, Ghorbanalinia M, et al. Endocannabinoids as endometrial inflammatory markers in lactating Holstein cows. Reprod Domest Anim. 2018;53(3):769–75.
pubmed: 29542183 doi: 10.1111/rda.13169
Bensaid M, Gary-Bobo M, Esclangon A, Maffrand JP, Le Fur G, Oury-Donat F, et al. The cannabinoid CB1 receptor antagonist SR141716 increases Acrp30 mRNA expression in adipose tissue of obese fa/fa rats and in cultured adipocyte cells. Mol Pharmacol. 2003;63(4):908–14.
pubmed: 12644592 doi: 10.1124/mol.63.4.908
Myers MN, Abou-Rjeileh U, Chirivi M, Parales-Girón J, Lock AL, Tam J, et al. Cannabinoid-1 receptor activation modulates lipid mobilization and adipogenesis in the adipose tissue of dairy cows. J Dairy Sci. 2023;106(5):3650–61.
pubmed: 36907764 doi: 10.3168/jds.2022-22556
Li X, Hua T, Vemuri K, Ho JH, Wu Y, Wu L, et al. Crystal structure of the human cannabinoid receptor CB2. Cell. 2019;176(3):459-467.e13.
pubmed: 30639103 pmcid: 6713262 doi: 10.1016/j.cell.2018.12.011
Zachut M, Kra G, Moallem U, Livshitz L, Levin Y, Udi S, et al. Characterization of the endocannabinoid system in subcutaneous adipose tissue in periparturient dairy cows and its association to metabolic profiles. PLoS One. 2018;13(11):e0205996.
pubmed: 30403679 pmcid: 6221292 doi: 10.1371/journal.pone.0205996
Ramirez-Orozco RE, Garcia-Ruiz R, Morales P, Villalon CM, Villafan-Bernal JR, Marichal-Cancino BA. Potential metabolic and behavioural roles of the putative endocannabinoid receptors GPR18, GPR55 and GPR119 in feeding. Curr Neuropharmacol. 2019;17(10):947–60.
pubmed: 31146657 pmcid: 7052828 doi: 10.2174/1570159X17666190118143014
Kasatkina LA, Rittchen S, Sturm EM. Neuroprotective and immunomodulatory action of the endocannabinoid system under neuroinflammation. Int J Mol Sci. 2021;22(11):5431.
pubmed: 34063947 pmcid: 8196612 doi: 10.3390/ijms22115431
Li Y, Chen X, Nie Y, Tian Y, Xiao X, Yang F. Endocannabinoid activation of the TRPV1 ion channel is distinct from activation by capsaicin. J Biol Chem. 2021;297:101022.
pubmed: 34332978 pmcid: 8387766 doi: 10.1016/j.jbc.2021.101022
Boczek T, Zylinska L. Receptor-dependent and independent regulation of voltage-gated Ca. Int J Mol Sci. 2021;22(15):8168.
pubmed: 34360934 pmcid: 8348342 doi: 10.3390/ijms22158168
Sun Y, Bennett A. Cannabinoids: a new group of agonists of PPARs. PPAR Res. 2007;2007:23513.
pubmed: 18288264 pmcid: 2220031 doi: 10.1155/2007/23513
Bouaboula M, Hilairet S, Marchand J, Fajas L, Le Fur G, Casellas P. Anandamide induced PPARgamma transcriptional activation and 3T3-L1 preadipocyte differentiation. Eur J Pharmacol. 2005;517(3):174–81.
pubmed: 15987634 doi: 10.1016/j.ejphar.2005.05.032
Kuipers EN, Kantae V, Maarse BCE, van den Berg SM, van Eenige R, Nahon KJ, et al. high fat diet increases circulating endocannabinoids accompanied by increased synthesis enzymes in adipose tissue. Front Physiol. 2018;9:1913.
pubmed: 30687125 doi: 10.3389/fphys.2018.01913
Tsuboi K, Uyama T, Okamoto Y, Ueda N. Endocannabinoids and related N-acylethanolamines: biological activities and metabolism. Inflamm Regen. 2018;38:28.
pubmed: 30288203 pmcid: 6166290 doi: 10.1186/s41232-018-0086-5
Mock ED, Gagestein B, van der Stelt M. Anandamide and other N-acylethanolamines: a class of signaling lipids with therapeutic opportunities. Prog Lipid Res. 2023;89:101194.
pubmed: 36150527 doi: 10.1016/j.plipres.2022.101194
Hillard CJ. Circulating endocannabinoids: from whence do they come and where are they going? Neuropsychopharmacology. 2018;43(1):155–72.
pubmed: 28653665 doi: 10.1038/npp.2017.130
Hillard CJ. Biochemistry and pharmacology of the endocannabinoids arachidonylethanolamide and 2-arachidonylglycerol. Prostaglandins Other Lipid Mediat. 2000;61(1–2):3–18.
pubmed: 10785538 doi: 10.1016/S0090-6980(00)00051-4
Hansen HS, Diep TA. N-acylethanolamines, anandamide and food intake. Biochem Pharmacol. 2009;78(6):553–60.
pubmed: 19413995 doi: 10.1016/j.bcp.2009.04.024
Yang L, Liang J, Lam SM, Yavuz A, Shui G, Ding M, et al. Neuronal lipolysis participates in PUFA-mediated neural function and neurodegeneration. EMBO reports. 2020;21(11):e50214.
pubmed: 33034119 pmcid: 7645260 doi: 10.15252/embr.202050214
Dinkla S, van Eijk LT, Fuchs B, Schiller J, Joosten I, Brock R, et al. Inflammation-associated changes in lipid composition and the organization of the erythrocyte membrane. BBA Clin. 2016;5:186–92.
pubmed: 27200268 pmcid: 4864322 doi: 10.1016/j.bbacli.2016.03.007
Snider NT, Walker VJ, Hollenberg PF. Oxidation of the endogenous cannabinoid arachidonoyl ethanolamide by the cytochrome P450 monooxygenases: physiological and pharmacological implications. Pharmacol Rev. 2010;62(1):136–54.
pubmed: 20133390 pmcid: 2835397 doi: 10.1124/pr.109.001081
Strieder-Barboza C, de Souza J, Raphael W, Lock AL, Contreras GA. Fetuin-A: a negative acute-phase protein linked to adipose tissue function in periparturient dairy cows. J Dairy Sci. 2018;101(3):2602–16.
pubmed: 29274966 doi: 10.3168/jds.2017-13644
Contreras GA, Thelen K, Schmidt SE, Strieder-Barboza C, Preseault CL, Raphael W, et al. Adipose tissue remodeling in late-lactation dairy cows during feed-restriction-induced negative energy balance. J Dairy Sci. 2016;99(12):10009–21.
pubmed: 27720147 doi: 10.3168/jds.2016-11552
Ney LJ, Felmingham KL, Bruno R, Matthews A, Nichols DS. Simultaneous quantification of endocannabinoids, oleoylethanolamide and steroid hormones in human plasma and saliva. J Chromatogr B. 2020;1152:122252.
pubmed: 32615536 doi: 10.1016/j.jchromb.2020.122252
Parkhomchuk D, Borodina T, Amstislavskiy V, Banaru M, Hallen L, Krobitsch S, et al. Transcriptome analysis by strand-specific sequencing of complementary DNA. Nucleic Acids Res. 2009;37(18):e123.
pubmed: 19620212 pmcid: 2764448 doi: 10.1093/nar/gkp596
Myers MN, Chirivi M, Gandy JC, Tam J, Zachut M, Contreras GA. Supplementary Table 1. Bulk RNA-seq read counts in bovine adipocytes following canonical and inflammatory lipolysis. figshare. Dataset. 2024. https://doi.org/10.6084/m9.figshare.25452160.v1 .
Mortazavi A, Williams BA, McCue K, Schaeffer L, Wold B. Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods. 2008;5(7):621–8.
pubmed: 18516045 doi: 10.1038/nmeth.1226
Pertea M, Pertea GM, Antonescu CM, Chang TC, Mendell JT, Salzberg SL. StringTie enables improved reconstruction of a transcriptome from RNA-seq reads. Nat Biotechnol. 2015;33(3):290–5.
pubmed: 25690850 pmcid: 4643835 doi: 10.1038/nbt.3122
Liao Y, Smyth GK, Shi W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics. 2014;30(7):923–30.
pubmed: 24227677 doi: 10.1093/bioinformatics/btt656
Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15(12):550.
pubmed: 25516281 pmcid: 4302049 doi: 10.1186/s13059-014-0550-8
Anders S, Huber W. Differential expression analysis for sequence count data. Genome Biol. 2010;11(10):R106.
pubmed: 20979621 pmcid: 3218662 doi: 10.1186/gb-2010-11-10-r106
Benjamini Y, Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. Series B ed. J Royal Stat Soc. 1995;57:289–300.
doi: 10.1111/j.2517-6161.1995.tb02031.x
Ge SX, Jung D, Yao R. ShinyGO: a graphical gene-set enrichment tool for animals and plants. Bioinformatics. 2020;36(8):2628–9.
pubmed: 31882993 doi: 10.1093/bioinformatics/btz931
Kanehisa M, Furumichi M, Tanabe M, Sato Y, Morishima K. KEGG: new perspectives on genomes, pathways, diseases and drugs. Nucleic Acids Res. 2017;45(D1):D353–61.
pubmed: 27899662 doi: 10.1093/nar/gkw1092
Myers MN, Chirivi M, Gandy JC, Tam J, Zachut M, Contreras GA. Supplementary Figure 1. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis used to compare the transcriptomic profiles of bovine adipocytes following bulk RNA-seq analysis. Figshare. Figure. 2024. https://doi.org/10.6084/m9.figshare.25961950.v1 .
Myers MN, Chirivi M, Gandy JC, Tam J, Zachut M, Contreras GA. Supplementary Table 2. Endocannabinoid system-associated genes of interest assessed in bulk RNA-seq analysis following canonical and inflammatory lipolysis in dairy cows' adipocytes. Figshare. Dataset. 2024. https://doi.org/10.6084/m9.figshare.25452274.v1 .
Dirandeh E, Ghaffari J. Effects of feeding a source of omega-3 fatty acid during the early postpartum period on the endocannabinoid system in the bovine endometrium. Theriogenology. 2018;121:141–6.
pubmed: 30145543 doi: 10.1016/j.theriogenology.2018.07.043
Buch C, Muller T, Leemput J, Passilly-Degrace P, Ortega-Deballon P, de Barros Pais JP, et al. Endocannabinoids produced by white adipose tissue modulate lipolysis in lean but not in obese rodent and human. Front Endocrinol (Lausanne). 2021;12:716431.
pubmed: 34434170 doi: 10.3389/fendo.2021.716431
Joosten MM, Balvers MG, Verhoeckx KC, Hendriks HF, Witkamp RF. Plasma anandamide and other N-acylethanolamines are correlated with their corresponding free fatty acid levels under both fasting and non-fasting conditions in women. Nutr Metab (Lond). 2010;7:49.
pubmed: 20546561 doi: 10.1186/1743-7075-7-49
Jones PJ, Lin L, Gillingham LG, Yang H, Omar JM. Modulation of plasma N-acylethanolamine levels and physiological parameters by dietary fatty acid composition in humans. J Lipid Res. 2014;55(12):2655–64.
pubmed: 25262934 pmcid: 4242457 doi: 10.1194/jlr.P051235
Kra G, Daddam JR, Moallem U, Kamer H, Mualem B, Levin Y, et al. Alpha-linolenic acid modulates systemic and adipose tissue-specific insulin sensitivity, inflammation, and the endocannabinoid system in dairy cows. Sci Rep. 2023;13:5280.
pubmed: 37002295 pmcid: 10066235 doi: 10.1038/s41598-023-32433-7
van Ackern I, Kuhla A, Kuhla B. A role for peripheral anandamide and 2-arachidonoylglycerol in short-term food intake and orexigenic hypothalamic responses in a species with continuous nutrient delivery. Nutrients. 2021;13(10):3587.
pubmed: 34684588 pmcid: 8540326 doi: 10.3390/nu13103587
Liu J, Wang L, Harvey-White J, Osei-Hyiaman D, Razdan R, Gong Q, et al. A biosynthetic pathway for anandamide. Proc Natl Acad Sci U S A. 2006;103(36):13345–50.
pubmed: 16938887 pmcid: 1557387 doi: 10.1073/pnas.0601832103
Jin W, Yang L, Yi Z, Fang H, Chen W, Hong Z, et al. Anti-inflammatory effects of fucoxanthinol in LPS-Induced RAW264.7 Cells through the NAAA-PEA pathway. Mar Drugs. 2020;18(4):222.
pubmed: 32326173 pmcid: 7230820 doi: 10.3390/md18040222
Melis M, Carta G, Pintus S, Pintus P, Piras CA, Murru E, et al. Polymorphism rs1761667 in the CD36 gene is associated to changes in fatty acid metabolism and circulating endocannabinoid levels distinctively in normal weight and obese subjects. Front Physiol. 2017;8:1006.
pubmed: 29270130 pmcid: 5724198 doi: 10.3389/fphys.2017.01006
Bryk M, Chwastek J, Kostrzewa M, Mlost J, Pędracka A, Starowicz K. Alterations in anandamide synthesis and degradation during osteoarthritis progression in an animal model. Int J Mol Sci. 2020;21(19):7381.
pubmed: 33036283 pmcid: 7582975 doi: 10.3390/ijms21197381
McFadden JW, Rico JE. Invited review: Sphingolipid biology in the dairy cow: The emerging role of ceramide. J Dairy Sci. 2019;102(9):7619–39.
pubmed: 31301829 doi: 10.3168/jds.2018-16095
Salcedo-Tacuma D, Parales-Giron J, Prom C, Chirivi M, Laguna J, Lock AL, et al. Transcriptomic profiling of adipose tissue inflammation, remodeling, and lipid metabolism in periparturient dairy cows (Bos taurus). BMC Genomics. 2020;21:824.
pubmed: 33228532 pmcid: 7686742 doi: 10.1186/s12864-020-07235-0
Liaw L, Prudovsky I, Koza RA, Anunciado-Koza RV, Siviski ME, Lindner V, et al. Lipid profiling of in vitro cell models of adipogenic differentiation: relationships with mouse adipose tissues. J Cell Biochem. 2016;117(9):2182–93.
pubmed: 26910604 pmcid: 4957144 doi: 10.1002/jcb.25522
Vanni S, Riccardi L, Palermo G, De Vivo M. Structure and dynamics of the acyl chains in the membrane trafficking and enzymatic processing of lipids. Acc Chem Res. 2019;52(11):3087–96.
pubmed: 31364837 doi: 10.1021/acs.accounts.9b00134
Briand-Mesange F, Pons V, Allart S, Masquelier J, Chicanne G, Beton N, et al. Glycerophosphodiesterase 3 (GDE3) is a lysophosphatidylinositol-specific ectophospholipase C acting as an endocannabinoid signaling switch. J Biol Chem. 2020;295(46):15767–81.
pubmed: 32917725 pmcid: 7667972 doi: 10.1074/jbc.RA120.015278
Murataeva N, Straiker A, Mackie K. Parsing the players: 2-arachidonoylglycerol synthesis and degradation in the CNS. Br J Pharmacol. 2014;171(6):1379–91.
pubmed: 24102242 pmcid: 3954479 doi: 10.1111/bph.12411
Facchinetti F, Del Giudice E, Furegato S, Passarotto M, Leon A. Cannabinoids ablate release of TNFalpha in rat microglial cells stimulated with lypopolysaccharide. Glia. 2003;41(2):161–8.
pubmed: 12509806 doi: 10.1002/glia.10177
Molina-Holgado F, Lledo A, Guaza C. Anandamide suppresses nitric oxide and TNF-alpha responses to Theiler’s virus or endotoxin in astrocytes. NeuroReport. 1997;8(8):1929–33.
pubmed: 9223079 doi: 10.1097/00001756-199705260-00027
Puffenbarger RA, Boothe AC, Cabral GA. Cannabinoids inhibit LPS-inducible cytokine mRNA expression in rat microglial cells. Glia. 2000;29(1):58–69.
pubmed: 10594923 doi: 10.1002/(SICI)1098-1136(20000101)29:1<58::AID-GLIA6>3.0.CO;2-W
Andres Contreras G, De Koster J, de Souza J, Laguna J, Mavangira V, Nelli RK, et al. Lipolysis modulates the biosynthesis of inflammatory lipid mediators derived from linoleic acid in adipose tissue of periparturient dairy cows. J Dairy Sci. 2020;103(2):1944–55.
pubmed: 31759597 doi: 10.3168/jds.2019-17256
Bradford BJ, Yuan K, Farney JK, Mamedova LK, Carpenter AJ. Invited review: inflammation during the transition to lactation: New adventures with an old flame. J Dairy Sci. 2015;98(10):6631–50.
pubmed: 26210279 doi: 10.3168/jds.2015-9683
Contreras GA, Kabara E, Brester J, Neuder L, Kiupel M. Macrophage infiltration in the omental and subcutaneous adipose tissues of dairy cows with displaced abomasum. J Dairy Sci. 2015;98(9):6176–87.
pubmed: 26117355 doi: 10.3168/jds.2015-9370
Putman AK, Gandy JC, Contreras GA, Sordillo LM. Oxylipids are associated with higher disease risk in postpartum cows. J Dairy Sci. 2022;105(3):2531–43.
pubmed: 35086706 doi: 10.3168/jds.2021-21057
Rico DE, Razzaghi A. Animal board invited review: the contribution of adipose stores to milk fat: implications on optimal nutritional strategies to increase milk fat synthesis in dairy cows. Animal. 2023;17(4):100735.
pubmed: 36889250 doi: 10.1016/j.animal.2023.100735
Kaczocha M, Glaser ST, Deutsch DG. Identification of intracellular carriers for the endocannabinoid anandamide. Proc Natl Acad Sci U S A. 2009;106(15):6375–80.
pubmed: 19307565 pmcid: 2669397 doi: 10.1073/pnas.0901515106
Oddi S, Fezza F, Pasquariello N, D’Agostino A, Catanzaro G, De Simone C, et al. Molecular identification of albumin and Hsp70 as cytosolic anandamide-binding proteins. Chem Biol. 2009;16(6):624–32.
pubmed: 19481477 doi: 10.1016/j.chembiol.2009.05.004
Gallegos AM, Atshaves BP, Storey SM, McIntosh AL, Petrescu AD, Schroeder F. Sterol carrier protein-2 expression alters plasma membrane lipid distribution and cholesterol dynamics. Biochemistry. 2001;40(21):6493–506.
pubmed: 11371213 doi: 10.1021/bi010217l
Gustafson B, Smith U. Regulation of white adipogenesis and its relation to ectopic fat accumulation and cardiovascular risk. Atherosclerosis. 2015;241(1):27–35.
pubmed: 25957567 doi: 10.1016/j.atherosclerosis.2015.04.812
Cheung SY, Huang Y, Kwan HY, Chung HY, Yao X. Activation of transient receptor potential vanilloid 3 channel suppresses adipogenesis. Endocrinology. 2015;156(6):2074–86.
pubmed: 25774551 doi: 10.1210/en.2014-1831
Ishac EJ, Jiang L, Lake KD, Varga K, Abood ME, Kunos G. Inhibition of exocytotic noradrenaline release by presynaptic cannabinoid CB1 receptors on peripheral sympathetic nerves. Br J Pharmacol. 1996;118(8):2023–8.
pubmed: 8864538 pmcid: 1909901 doi: 10.1111/j.1476-5381.1996.tb15639.x
Liu J, Batkai S, Pacher P, Harvey-White J, Wagner JA, Cravatt BF, et al. Lipopolysaccharide induces anandamide synthesis in macrophages via CD14/MAPK/phosphoinositide 3-kinase/NF-kappaB independently of platelet-activating factor. J Biol Chem. 2003;278(45):45034–9.
pubmed: 12949078 doi: 10.1074/jbc.M306062200

Auteurs

Madison N Myers (MN)

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI, 48824, USA.

Miguel Chirivi (M)

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI, 48824, USA.

Jeff C Gandy (JC)

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI, 48824, USA.

Joseph Tam (J)

Obesity and Metabolism Laboratory, The Institute for Drug Research, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, 9112001, Israel.

Maya Zachut (M)

Department of Ruminant Science, Institute of Animal Sciences, Agricultural Research Organization Volcani Institute, Rishon LeZion, 7505101, Israel.

G Andres Contreras (GA)

Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, MI, 48824, USA. contre28@msu.edu.

Classifications MeSH