N-Acylamides

N-acyl amides are a general class of endogenous fatty acid compounds characterized by a fatty acyl group linked to a primary amine metabolite by an amide bond. Broadly speaking, N-acyl amides fall into several categories: amino acid conjugates (e.g., N-arachidonoyl-glycine), neurotransmitter conjugates (e.g., N-arachidonoyl-serotonin), ethanolamine conjugates (e.g., anandamide), and taurine conjugates (e.g., N-palmitoyl-taurine). N-acyl amides have pleiotropic signaling functions in physiology, including in cardiovascular function, metabolic homeostasis, memory, cognition, pain, motor control and others.[1] Initial attention focused on N-acyl amides present in mammalian organisms, however recently lipid signaling systems consisting of N-acyl amides have also been found to be present in invertebrates, such as Drosophila melanogaster.[2] N-acyl amides play important roles in many biochemical pathways involved in a variety of physiological and pathological processes, as well as the metabolic enzymes, transporters, and receptors that regulate their signaling.

Compounds
ClassCommon Name
2-acyl glycerols2-oleoyl glycerol † #
2-linoleoyl glycerol † # *
2-arachidonoyl glycerol †
N-acyl alanineN-palmitoyl alanine † #
N-stearoyl alanine † #
N-oleoyl alanine † #
N-linoleoyl alanine #
N-arachidonoyl alanine †
N-docosahexaenoyl alanine †
N-acyl ethanolamineN-lauroylethanolamine *
N-myristoylethanolamine *
N-palmitoyl ethanolamine † # *
N-stearoyl ethanolamine † #
N-oleoyl ethanolamine † #
N-linoleoyl ethanolamine † #
N-arachidonoyl ethanolamine †
N-docosahexaenoyl ethanolamine †
N-acyl dopamineN-palmitoyl dopamine †
N-stearoyl dopamine †
N-oleoyl dopamine †
N-arachidonoyl dopamine †
N-acyl GABAN-palmitoyl GABA †
N-stearoyl GABA †
N-oleoyl GABA † #
N-linoleoyl GABA #
N-arachidonoyl GABA †
N-docosahexaenoyl GABA †
N-acyl glycineN-palmitoyl glycine † #
N-stearoyl glycine † #
N-oleoyl glycine † #
N-linoleoyl glycine † #
N-arachidonoyl glycine †
N-docosahexaenoyl glycine †
N-acyl leucineN-palmitoyl leucine † #
N-stearoyl leucine #
N-oleoyl leucine † #
N-linoleoyl leucine #
N-docosahexaenoyl leucine †
N-acyl methionineN-palmitoyl methionine † #
N-stearoyl methionine †
N-oleoyl methionine † #
N-linoleoyl methionine #
N-arachidonoyl methionine †
N-docosahexaenoyl methionine †
N-acyl phenylalanineN-palmitoyl phenylalanine † #
N-stearoyl phenylalanine † #
N-oleoyl phenylalanine † #
N-linoleoyl phenylalanine #
N-arachidonoyl phenylalanine †
N-docosahexaenoyl phenylalanine †
N-acyl prolineN-palmitoyl proline † #
N-stearoyl proline † #
N-oleoyl proline † #
N-linoleoyl proline #
N-arachidonoyl proline †
N-docosahexaenoyl proline †
N-acyl serotoninN-palmitoyl serotonin †
N-stearoyl serotonin †
N-oleoyl serotonin †
N-eicosapentaenoyl serotonin †
N-arachidonoyl serotonin †
N-docosahexaenoyl serotonin †
N-acyl serineN-palmitoyl serine † #
N-stearoyl serine † #
N-oleoyl serine † #
N-linoleoyl serine #
N-arachidonoyl serine †
N-docosahexaenoyl serine †
N-acyl taurineN-palmitoyl taurine †
N-stearoyl taurine †
N-arachidonoyl taurine †
N-acyl tryptophanN-palmitoyl tryptophan † #
N-stearoyl tryptophan † #
N-oleoyl tryptophan † #
N-linoleoyl tryptophan #
N-arachidonoyl tryptophan †
N-docosahexaenoyl tryptophan †
N-acyl tyrosineN-palmitoyl tyrosine † #
N-stearoyl tyrosine † #
N-oleoyl tyrosine † #
N-linoleoyl tyrosine #
N-arachidonoyl tyrosine †
N-docosahexaenoyl tyrosine †
N-acyl valineN-palmitoyl valine † #
N-stearoyl valine † #
N-oleoyl valine † #
N-nervonoyl valine †
N-linoleoyl valine #
N-docosahexaenoyl valine †

†-Compound found in mammalian species[2][3][4][5][6][7][8][9][10][11]

#-Compound found in invertebrate (Drosophila melanogaster) species[2][12][13][14]

*-Compound found in plant species[15][16][17][18]

Enzymatic biosynthesis and degradation

The enzymatic biosynthesis of the N-acyl amide class of metabolites is a topic of active research with various pathways being discovered for specific N-acyl amides. For example, a proposed biosynthetic pathway for the N-acyl ethanolamines (NAEs) has been the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a phospholipase D activity to liberate NAE and, as a byproduct, phosphatidic acid. Mice deficient in the enzyme NAPE-PLD show decreased in a subset of brain NAEs, providing genetic evidence for this proposal, at least for a subset of the NAEs. Other biosynthetic pathways do exist and are currently being elucidated. Two possible alternative routes are via lysoNAPE or phosphate-NAE.

The degradation of NAEs in vivo is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of NAEs into fatty acids and ethanolamine. Mice deficient in FAAH show complete loss of NAE degradation activity in tissues and dramatic elevations in tissue levels of NAEs.

FAAH also mediates the degradation of a separate class of N-acyl amides, the N-acyl taurines (NATs). FAAH knockout mice also show dramatic increases in tissue and blood NATs. The enzymatic biosynthesis of NATs remains unknown.

A distinct circulating enzyme, peptidase M20 domain containing 1 (PM20D1), can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids in vitro. In vivo, PM20D1 overexpression increases the levels of various N-acyl amino acids in blood, demonstrating that this enzyme can contribute to N-acyl amino acid biosynthesis.[19] PM20D1 knockout mice have complete loss of N-acyl amino acid hydrolysis activity in blood and tissues with concomitant bidirectional dysregulation of endogenous N-acyl amino acids.[20]

Biological Activity

N-acyl amides have been shown to play an important role in a variety of physiological functions as lipid signaling molecule. Apart from the aforementioned roles in cardiovascular function, memory, cognition, pain, and motor control, the compounds have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity.[11]

In a more general sense, one of the key characteristics of the N-acyl amide group of compounds is their ubiquitous nature. Research has shown the presence of the compounds in mice, Drosophila melanogaster, Arabidopsis, C. Elegans, Cerevisiae (yeast), Pseudomonas Syringae, olive oil and PYD media[21] . This diverse presence of N-acyl amides attests to their importance in multiple biological systems and also shows that the detected presence of specific N-acyl amides in a number of species, including humans, may be endogenous or exogenous.

N-acyl amides are primarily involved in cell-to-cell communication in biological systems. An example of this is the lipid signaling system involving transient receptor potential channels (TRP), which interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion.[22] This signaling system has been shown to play a role in the physiological processes involved in inflammation.[23] Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists.[20]

An application of N-acyl amides that is currently at the forefront of related research is the correlation between oleoyl serine and bone remodeling. Recent research has shown that oleoyl serine, an N-acyl amide found in olive oil amongst other sources, plays a role in the proliferation of osteoblast activity and the inhibition of osteoclast activity.[24] Further research regarding this application of oleoyl serine is set to take place to explore the possible correlation between the consumption of the compound by individuals at risk for osteoporosis.

Certain N-acyl amino acids can act as chemical uncouplers and directly stimulate mitochondrial respiration. These N-acyl amino acids are characterized by medium chain, unsaturated fatty acyl chains and neutral amino acid head groups.[25] Administration of these N-acyl amino acids to mice elevates energy expenditure leading to profound body weight loss and improvement of glucose homeostasis.[26]

Overall, the applications of N-acyl amides in biological settings are abundant. As mentioned, their importance in cell signaling in a variety systems leading to various physiological roles and in turn therapeutic capabilities, which gives all the more reason to continue the extensive research being conducted on the compounds today.

Several N-acyl amides have been demonstrated to physiologically activate G-protein coupled receptors. Anandamide activates the cannabinoid receptors CB1 and CB2. FAAH knockout mice show increased anandamide levels in vivo and cannabinoid-receptor dependent behaviors including antinociception and anxiolysis. GPR18, GPR55, GPR92 have also been proposed to be activated by various N-acyl amides, though the physiological relevance of these assignments remains unknown.

References
  1. Bradshaw HB, Walker JM (February 2005). "The expanding field of cannabimimetic and related lipid mediators". British Journal of Pharmacology. 144 (4): 459–65. doi:10.1038/sj.bjp.0706093. PMC 1576036. PMID 15655504.
  2. Tortoriello G, Rhodes BP, Takacs SM, Stuart JM, Basnet A, Raboune S, Widlanski TS, Doherty P, Harkany T, Bradshaw HB (2013). "Targeted lipidomics in Drosophila melanogaster identifies novel 2-monoacylglycerols and N-acyl amides". PLOS ONE. 8 (7): e67865. Bibcode:2013PLoSO...867865T. doi:10.1371/journal.pone.0067865. PMC 3708943. PMID 23874457.
  3. Ben-Shabat S, Fride E, Sheskin T, Tamiri T, Rhee MH, Vogel Z, Bisogno T, De Petrocellis L, Di Marzo V, Mechoulam R (July 1998). "An entourage effect: inactive endogenous fatty acid glycerol esters enhance 2-arachidonoyl-glycerol cannabinoid activity". European Journal of Pharmacology. 353 (1): 23–31. doi:10.1016/s0014-2999(98)00392-6. PMID 9721036.
  4. Bisogno T, Katayama K, Melck D, Ueda N, De Petrocellis L, Yamamoto S, Di Marzo V (June 1998). "Biosynthesis and degradation of bioactive fatty acid amides in human breast cancer and rat pheochromocytoma cells--implications for cell proliferation and differentiation". European Journal of Biochemistry. 254 (3): 634–42. doi:10.1046/j.1432-1327.1998.2540634.x. PMID 9688276.
  5. Bradshaw HB, Rimmerman N, Hu SS, Burstein S, Walker JM (2009). Novel endogenous N-acyl glycines identification and characterization. Vitamins & Hormones. 81. pp. 191–205. doi:10.1016/S0083-6729(09)81008-X. ISBN 9780123747822. PMID 19647113.
  6. Chu CJ, Huang SM, De Petrocellis L, Bisogno T, Ewing SA, Miller JD, Zipkin RE, Daddario N, Appendino G, Di Marzo V, Walker JM (April 2003). "N-oleoyldopamine, a novel endogenous capsaicin-like lipid that produces hyperalgesia". The Journal of Biological Chemistry. 278 (16): 13633–9. doi:10.1074/jbc.M211231200. PMID 12569099.
  7. Salzet M, Breton C, Bisogno T, Di Marzo V (August 2000). "Comparative biology of the endocannabinoid system possible role in the immune response". European Journal of Biochemistry. 267 (16): 4917–27. doi:10.1046/j.1432-1327.2000.01550.x. PMID 10931174.
  8. Tan B, O'Dell DK, Yu YW, Monn MF, Hughes HV, Burstein S, Walker JM (January 2010). "Identification of endogenous acyl amino acids based on a targeted lipidomics approach". Journal of Lipid Research. 51 (1): 112–9. doi:10.1194/jlr.M900198-JLR200. PMC 2789771. PMID 19584404.
  9. Tan B, Yu YW, Monn MF, Hughes HV, O'Dell DK, Walker JM (September 2009). "Targeted lipidomics approach for endogenous N-acyl amino acids in rat brain tissue". Journal of Chromatography B. 877 (26): 2890–4. doi:10.1016/j.jchromb.2009.01.002. PMID 19168403.
  10. Verhoeckx KC, Voortman T, Balvers MG, Hendriks HF, M Wortelboer H, Witkamp RF (October 2011). "Presence, formation and putative biological activities of N-acyl serotonins, a novel class of fatty-acid derived mediators, in the intestinal tract". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1811 (10): 578–86. doi:10.1016/j.bbalip.2011.07.008. PMID 21798367.
  11. Waluk DP (2012). Biosynthesis and physiological functions of N-acyl amino acids (PDF) (Ph.D. thesis). Stockholm University.
  12. Elphick MR, Satou Y, Satoh N (January 2003). "The invertebrate ancestry of endocannabinoid signalling: an orthologue of vertebrate cannabinoid receptors in the urochordate Ciona intestinalis". Gene. 302 (1–2): 95–101. doi:10.1016/s0378-1119(02)01094-6. PMID 12527200.
  13. Fezza F, Dillwith JW, Bisogno T, Tucker JS, Di Marzo V, Sauer JR (July 2003). "Endocannabinoids and related fatty acid amides, and their regulation, in the salivary glands of the lone star tick". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1633 (1): 61–7. doi:10.1016/s1388-1981(03)00087-8. PMID 12842196.
  14. Salzet M, Stefano GB (2002). "The endocannabinoid system in invertebrates". Prostaglandins, Leukotrienes, and Essential Fatty Acids. 66 (2–3): 353–61. doi:10.1054/plef.2001.0347. PMID 12052049.
  15. Chapman KD (November 2000). "Emerging physiological roles for N-acylphosphatidylethanolamine metabolism in plants: signal transduction and membrane protection". Chemistry and Physics of Lipids. 108 (1–2): 221–9. doi:10.1016/s0009-3084(00)00198-5. PMID 11106793.
  16. Chapman KD (July 2004). "Occurrence, metabolism, and prospective functions of N-acylethanolamines in plants". Progress in Lipid Research. 43 (4): 302–27. doi:10.1016/j.plipres.2004.03.002. PMID 15234550.
  17. Chapman KD, Tripathy S, Venables B, Desouza AD (March 1998). "N-Acylethanolamines: formation and molecular composition of a new class of plant lipids". Plant Physiology. 116 (3): 1163–8. doi:10.1104/pp.116.3.1163. PMC 35086. PMID 9501149.
  18. Lee SM, Radhakrishnan R, Kang SM, Kim JH, Lee IY, Moon BK, Yoon BW, Lee IJ (December 2015). "Phytotoxic mechanisms of bur cucumber seed extracts on lettuce with special reference to analysis of chloroplast proteins, phytohormones, and nutritional elements". Ecotoxicology and Environmental Safety. 122: 230–7. doi:10.1016/j.ecoenv.2015.07.015. PMID 26277540.
  19. Long JZ, Svensson KJ, Bateman LA, Lin H, Kamenecka T, Lokurkar IA, Lou J, Rao RR, Chang MR, Jedrychowski MP, Paulo JA, Gygi SP, Griffin PR, Nomura DK, Spiegelman BM (July 2016). "The Secreted Enzyme PM20D1 Regulates Lipidated Amino Acid Uncouplers of Mitochondria". Cell. 166 (2): 424–435. doi:10.1016/j.cell.2016.05.071. PMC 4947008. PMID 27374330.
  20. Long JZ, Roche AM, Berdan CA, Louie SM, Roberts AJ, Svensson KJ, Dou FY, Bateman LA, Mina AI, Deng Z, Jedrychowski MP, Lin H, Kamenecka TM, Asara JM, Griffin PR, Banks AS, Nomura DK, Spiegelman BM (July 2018). "N-acyl amino acid control of metabolism and nociception". Proceedings of the National Academy of Sciences of the United States of America. 115 (29): E6937–E6945. doi:10.1073/pnas.1803389115. PMC 6055169. PMID 29967167.
  21. Bradshaw, Heather B.,Leishman, Emma. “Expanding the range of potential “endogenous cannabinoids” to incorporate lipids in bacteria, yeast, worms, and flies: cannabimimetic lipids are not just from arachidonic acid anymore.” IRCS Poster Presentation. 2013.
  22. Bradshaw HB, Raboune S, Hollis JL (March 2013). "Opportunistic activation of TRP receptors by endogenous lipids: exploiting lipidomics to understand TRP receptor cellular communication". Life Sciences. 92 (8–9): 404–9. doi:10.1016/j.lfs.2012.11.008. PMC 3587287. PMID 23178153.
  23. Raboune S, Stuart JM, Leishman E, Takacs SM, Rhodes B, Basnet A, Jameyfield E, McHugh D, Widlanski T, Bradshaw HB (2014). "Novel endogenous N-acyl amides activate TRPV1-4 receptors, BV-2 microglia, and are regulated in brain in an acute model of inflammation". Frontiers in Cellular Neuroscience. 8: 195. doi:10.3389/fncel.2014.00195. PMC 4118021. PMID 25136293.
  24. Smoum R, Bar A, Tan B, Milman G, Attar-Namdar M, Ofek O, Stuart JM, Bajayo A, Tam J, Kram V, O'Dell D, Walker MJ, Bradshaw HB, Bab I, Mechoulam R (October 2010). "Oleoyl serine, an endogenous N-acyl amide, modulates bone remodeling and mass". Proceedings of the National Academy of Sciences of the United States of America. 107 (41): 17710–5. Bibcode:2010PNAS..10717710S. doi:10.1073/pnas.0912479107. PMC 2955099. PMID 20876113.
  25. Lin H, Long JZ, Roche AM, Svensson KJ, Dou FY, Chang MR, Strutzenberg T, Ruiz C, Cameron MD, Novick SJ, Berdan CA, Louie SM, Nomura DK, Spiegelman BM, Griffin PR, Kamenecka TM (April 2018). "Discovery of Hydrolysis-Resistant Isoindoline N-Acyl Amino Acid Analogues that Stimulate Mitochondrial Respiration". Journal of Medicinal Chemistry. 61 (7): 3224–3230. doi:10.1021/acs.jmedchem.8b00029. PMC 6335027. PMID 29533650.
  26. Long JZ, Svensson KJ, Bateman LA, Lin H, Kamenecka T, Lokurkar IA, et al. (July 2016). "The Secreted Enzyme PM20D1 Regulates Lipidated Amino Acid Uncouplers of Mitochondria". Cell. 166 (2): 424–435. doi:10.1016/j.cell.2016.05.071. PMC 4947008. PMID 27374330.
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