Coronaric acid

Coronaric acid (isoleukotoxin) is a mono-unsaturated, epoxide derivative of the di-saturated fatty acid, linoleic acid (i.e. 9(Z),12(Z) octadecadienoic acid. It is a mixture of the two optically active isomers of 12(Z) 9,10-epoxy-octadecenoic acid. This mixture is also termed 9,10-epoxy-12Z-octadecenoic acid or 9(10)-EpOME[1] and when formed by or studied in mammalians, isoleukotoxin.

Coronaric acid
Names
IUPAC name
8-[3-[(Z)-Oct-2-enyl]oxiran-2-yl]octanoic acid
Other names
9,10-Epoxy-12Z-octadecenoic acid; 9(10)-EpOME
Identifiers
3D model (JSmol)
Properties
C18H32O3
Molar mass 296.451 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Occurrence

Coronaric acid is found in the seed oils derived from plants in sunflower family such as (Helianthus annuus)[2] and Xeranthemum annuum.[3]

Coronaric acid is also formed by the cells and tissues of various mammalian (including humans) species through the metabolism of linoleic acid by cytochrome P450 (CYP) epoxygenase enzymes. These CYPs (CYP2C9 and probably other CYPs that metabolize polyunsaturated fatty acids to epoxides) metabolize linoleic acid to (+)12S,13R-epoxy-9(Z)-octadecaenoic acid and (-)12R,13S-epoxy-9(Z)-octadecaenoic acid, i.e. the (+) and (-) epoxy optical isomers of coronaric acid.[4][5][6] When studied in this context, the optical isomer mixture is often termed isoleukotoxin. This same CYP epoxygenases concurrently attack linoleic acid at the carbon 9,10 rather than 12,13 double bond of linoleic acid to form a mixture of (+) and (-) epoxy optical isomers viz., 9S,10R-epoxy-12(Z)-octadecaenoic and 9R,10S-epoxy-12(Z)-octadecaenoic acids. This (+) and (-) optical mixture is often termed vernolic acid or when studied in plants and leukotoxin when studied in mammals.[4][5][6]

Coronoric acid is found in urine samples from healthy human subjects and increases 3- to 4-fold when these subjects are treated with a salt-loading diet.[5]

Coronaric and vernolic acids also form non-enzymatically when linoleic acid is exposed to oxygen and/or UV radiation as a result of the spontaneous process of autooxidation.[7] This autoxidation complicates studies in that it is often difficult to determine if these epoxy fatty acids identified in linoleic acid-rich plant and mammalian tissues represent actual tissue contents or are artifacts formed during their isolation and detection.

Metabolism

In mammalian tissue, coronaric acid is metabolized to its two corresponding dihydroxy stereoisomers, 12S,13R-dihydroxy-9(Z)-octadecaenoic and 12R,13S-dihydroxy-9(Z)-octadecaenoic acids, by soluble epoxide hydrolase within minutes of its formation.[8] The metabolism of coronaric acid to these two products, collectively termed isoleukotoxin diols, appears to be critical to coronaric acid's toxicity, i.e. the diols are the toxic metabolites of the non-toxic or far less toxic coronaric acid.[8][9][6]

Activities

Toxicities

At very high concentrations, the linoleic acid-derived set of optical isomers, coronaric acid (i.e. isoleukotoxin), possesses activities similar to that of other structurally unrelated leukotoxins viz., It is toxic to leukocytes and other cell types and when injected into rodents produce multiple organ failure and respiratory distress.[10][11][12][6] These effects appear due to its conversion to its dihydroxy counterparts, 9S,10R- and 9R,10S-dihydroxy-12(Z)-octadecaenoic acids by soluble epoxide hydrolase.[8] Some studies suggest but have not yet proven that isoleukotoxin, acting primarily if not exclusively through its dihydroxy counterparts, is responsible for or contribute to multiple organ failure, the acute respiratory distress syndrome, and certain other cataclysmic diseases in humans (see epoxygenase section on linoleic acid).[11][13][9] Vernolic acid (i.e. leukotoxin) shares a similar metabolic fate in being converted by soluble epoxide hydrolase to its dihydroxide counterparts and toxic actions of these hydroxide counterparts.

Other activities

At lower concentrations, isoleukotoxin and its dihydroxy counterparts can protect from the toxic actions cited above that occur at higher concentrations of isoleukotoxin and leukotoxin; they may also share with the epoxides of arachidonic acid, i.e. the epoxyeicosatreienoates (see Epoxyeicosatrienoic acids), anti-hypertension activities.[5]

References
  1. https://pubchem.ncbi.nlm.nih.gov/compound/6246154
  2. Mikolajczak, K. L.; Freidinger, R. M.; Smith Jr, C. R.; Wolff, I. A. (1968). "Oxygenated fatty acids of oil from sunflower seeds after prolonged storage". Lipids. 3 (6): 489–94. doi:10.1007/BF02530891. PMID 17805802. S2CID 4028426.
  3. Powell, R. G.; Smith Jr, C. R.; Wolff, I. A. (1967). "Cis-5,cis-9,cis-12-octadecatrienoic and some unusual oxygenated acids in Xeranthemum annuum seed oil". Lipids. 2 (2): 172–7. doi:10.1007/BF02530918. PMID 17805745. S2CID 3994480.
  4. Draper, A. J.; Hammock, B. D. (2000). "Identification of CYP2C9 as a human liver microsomal linoleic acid epoxygenase" (PDF). Archives of Biochemistry and Biophysics. 376 (1): 199–205. doi:10.1006/abbi.2000.1705. PMID 10729206. S2CID 21213904.
  5. Konkel, A; Schunck, W. H. (2011). "Role of cytochrome P450 enzymes in the bioactivation of polyunsaturated fatty acids". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1814 (1): 210–22. doi:10.1016/j.bbapap.2010.09.009. PMID 20869469.
  6. Spector, A. A.; Kim, H. Y. (2015). "Cytochrome P450 epoxygenase pathway of polyunsaturated fatty acid metabolism". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1851 (4): 356–65. doi:10.1016/j.bbalip.2014.07.020. PMC 4314516. PMID 25093613.
  7. Sevanian, A; Mead, J. F.; Stein, R. A. (1979). "Epoxides as products of lipid autoxidation in rat lungs". Lipids. 14 (7): 634–43. doi:10.1007/bf02533449. PMID 481136. S2CID 4036806.
  8. Greene, J. F.; Newman, J. W.; Williamson, K. C.; Hammock, B. D. (2000). "Toxicity of epoxy fatty acids and related compounds to cells expressing human soluble epoxide hydrolase". Chemical Research in Toxicology. 13 (4): 217–26. doi:10.1021/tx990162c. PMID 10775319.
  9. Edwards, L. M.; Lawler, N. G.; Nikolic, S. B.; Peters, J. M.; Horne, J; Wilson, R; Davies, N. W.; Sharman, J. E. (2012). "Metabolomics reveals increased isoleukotoxin diol (12,13-DHOME) in human plasma after acute Intralipid infusion". The Journal of Lipid Research. 53 (9): 1979–86. doi:10.1194/jlr.P027706. PMC 3413237. PMID 22715155.
  10. Moran, J. H.; Weise, R; Schnellmann, R. G.; Freeman, J. P.; Grant, D. F. (1997). "Cytotoxicity of linoleic acid diols to renal proximal tubular cells". Toxicology and Applied Pharmacology. 146 (1): 53–9. doi:10.1006/taap.1997.8197. PMID 9299596.
  11. Greene, J. F.; Hammock, B. D. (1999). "Toxicity of linoleic acid metabolites". Advances in Experimental Medicine and Biology. 469: 471–7. doi:10.1007/978-1-4615-4793-8_69. ISBN 978-1-4613-7171-7. PMID 10667370.
  12. Linhartová, I; Bumba, L; Mašín, J; Basler, M; Osička, R; Kamanová, J; Procházková, K; Adkins, I; Hejnová-Holubová, J; Sadílková, L; Morová, J; Sebo, P (2010). "RTX proteins: A highly diverse family secreted by a common mechanism". FEMS Microbiology Reviews. 34 (6): 1076–112. doi:10.1111/j.1574-6976.2010.00231.x. PMC 3034196. PMID 20528947.
  13. Zheng, J; Plopper, C. G.; Lakritz, J; Storms, D. H.; Hammock, B. D. (2001). "Leukotoxin-diol: A putative toxic mediator involved in acute respiratory distress syndrome". American Journal of Respiratory Cell and Molecular Biology. 25 (4): 434–8. doi:10.1165/ajrcmb.25.4.4104. PMID 11694448.
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