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Tuesday 25 July 2017

Anti-inflammatory ω-3 endocannabinoid epoxides


http://www.pnas.org/content/114/30/E6034

  1. Aditi Dasa,c,f,i,k,1
  1. aDepartment of Comparative Biosciences, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  2. bMedical Scholars Program, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  3. cDepartment of Biochemistry, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  4. dDepartment of Materials Science and Engineering, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  5. eDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109;
  6. fDivision of Nutritional Sciences, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  7. gCollege of Veterinary Medicine, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  8. hDepartment of Animal Sciences, University of Illinois at Urbana–Champaign, Champaign, IL 61801;
  9. iDepartment of Bioengineering, University of Illinois at Urbana–Champaign, Champaign IL 61801;
  10. jDivision of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI 48109;
  11. kBeckman Institute for Advanced Science and Technology, University of Illinois at Urbana–Champaign, Champaign, IL 61801
  1. Edited by Benjamin F. Cravatt, The Scripps Research Institute, La Jolla, CA, and approved June 6, 2017 (received for review June 24, 2016)

Significance

The health benefits of ω-3 fatty acids are mediated, in part, through metabolic conversion to bioactive epoxides. Here we detail the discovery and initial characterization of naturally occurring ω-3–derived endocannabinoid epoxides that are formed via enzymatic oxidation of ω-3 endocannabinoids by cytochrome P450s. These dual functional ω-3 endocannabinoid epoxides are anti-inflammatory and vasodilatory and reciprocally modulate platelet aggregation. By virtue of their physiological properties, they are expected to play important roles in neuroinflammation and in cerebrovascular diseases such as stroke.

Abstract

Clinical studies suggest that diets rich in ω-3 polyunsaturated fatty acids (PUFAs) provide beneficial anti-inflammatory effects, in part through their conversion to bioactive metabolites. Here we report on the endogenous production of a previously unknown class of ω-3 PUFA–derived lipid metabolites that originate from the crosstalk between endocannabinoid and cytochrome P450 (CYP) epoxygenase metabolic pathways. The ω-3 endocannabinoid epoxides are derived from docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) to form epoxyeicosatetraenoic acid-ethanolamide (EEQ-EA) and epoxydocosapentaenoic acid-ethanolamide (EDP-EA), respectively. Both EEQ-EAs and EDP-EAs are endogenously present in rat brain and peripheral organs as determined via targeted lipidomics methods. These metabolites were directly produced by direct epoxygenation of the ω-3 endocannabinoids, docosahexanoyl ethanolamide (DHEA) and eicosapentaenoyl ethanolamide (EPEA) by activated BV-2 microglial cells, and by human CYP2J2. Neuroinflammation studies revealed that the terminal epoxides 17,18-EEQ-EA and 19,20-EDP-EA dose-dependently abated proinflammatory IL-6 cytokines while increasing anti-inflammatory IL-10 cytokines, in part through cannabinoid receptor-2 activation. Furthermore the ω-3 endocannabinoid epoxides 17,18-EEQ-EA and 19,20-EDP-EA exerted antiangiogenic effects in human microvascular endothelial cells (HMVEC) and vasodilatory actions on bovine coronary arteries and reciprocally regulated platelet aggregation in washed human platelets. Taken together, the ω-3 endocannabinoid epoxides’ physiological effects are mediated through both endocannabinoid and epoxyeicosanoid signaling pathways. In summary, the ω-3 endocannabinoid epoxides are found at concentrations comparable to those of other endocannabinoids and are expected to play critical roles during inflammation in vivo; thus their identification may aid in the development of therapeutics for neuroinflammatory and cerebrovascular diseases.

Footnotes

  • 1To whom correspondence should be addressed. Email: aditidas{at}illinois.edu.
  • Author contributions: D.R.M., J.E.W., A.A.A., R.A., M.P.C., R.W.J., K.A.K., M.H., and A.D. designed research; D.R.M., J.E.W., A.A.A., R.A., M.P.C., and J.E.K. performed research; D.R.M. and A.D. contributed new reagents/analytic tools; D.R.M., J.E.W., A.A.A., R.A., M.P.C., R.W.J., K.A.K., M.H., and A.D. analyzed data; and D.R.M., J.E.W., A.A.A., R.A., R.W.J., K.A.K., M.H., and A.D. wrote the paper.
  • The authors declare no conflict of interest.
  • This article is a PNAS Direct Submission.
  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1610325114/-/DCSupplemental.
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