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British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1992 Feb;105(2):297–304. doi: 10.1111/j.1476-5381.1992.tb14249.x

Hepoxilins sensitize blood vessels to noradrenaline--stereospecificity of action.

O Laneuville 1, R Couture 1, C R Pace-Asciak 1
PMCID: PMC1908669  PMID: 1559126

Abstract

1. The vascular activity of two stereoisomers of hepoxilin A3 (HxA3) (8R and 8S) and of its glutathione conjugate, hepoxilin A3-C (HxA3-C) (8R and 8S), was investigated on rat helicoidal strips of thoracic aorta and longitudinal strips of portal vein. 2. Neither of the hepoxilins tested had a direct effect on the tone of the aortic strip or on the spontaneous contractions of the portal vein. However, the noradrenaline (NA)-induced response of these vessels, as expressed by the dose required for half maximal contraction, (EC50) was greater in HxA3 (8S)- and HxA3-C (8R)-treated aorta. Increased frequency and strength of spontaneous contractions of the portal vein were detected at lower concentrations of NA in the presence of hepoxilins. 3. The threshold dose for both hepoxilins was 10(-8) M and their effect was not dose-related beyond 10(-8) M. The effect of hepoxilin appeared after a 45 min incubation period and could be observed even if the compounds were washed out after 15 min. 4. Stereochemical specificity was observed. The 8S isomer of HxA3 was active in potentiating the NA-induced contraction of these vessels while the 8R isomer was inactive. In contrast, the 8R isomer of HxA3-C was active while the 8S isomer was inactive. In both tissues, HxA3 (8S) was more potent than its glutathione conjugate, HxA3-C (8R). 5. In calcium-free buffer or in the presence of a calcium channel blocker (nifedipine 1 microM), no potentiation of NA-induced contraction by hepoxilins could be observed, suggesting the involvement of extracellular calcium in the actions of hepoxilins.(ABSTRACT TRUNCATED AT 250 WORDS)

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Selected References

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  1. Bohr D. F. Vascular Smooth Muscle: Dual Effect of Calcium. Science. 1963 Feb 15;139(3555):597–599. doi: 10.1126/science.139.3555.597. [DOI] [PubMed] [Google Scholar]
  2. Cohen M. L., Berkowitz B. A. Decreased vascular relaxation in hypertension. J Pharmacol Exp Ther. 1976 Feb;196(2):396–406. [PubMed] [Google Scholar]
  3. Couture R., Rioux F., Regoli D. Vascular reactivity to angiotensin and noradrenaline following nephrectomy in rats. Clin Exp Hypertens. 1978;1(3):393–405. doi: 10.3109/10641967809068615. [DOI] [PubMed] [Google Scholar]
  4. Derewlany L. O., Pace-Asciak C. R., Radde I. C. Hepoxilin A, hydroxyepoxide metabolite of arachidonic acid, stimulates transport of 45Ca across the guinea pig visceral yolk sac. Can J Physiol Pharmacol. 1984 Dec;62(12):1466–1469. doi: 10.1139/y84-243. [DOI] [PubMed] [Google Scholar]
  5. Dho S., Grinstein S., Corey E. J., Su W. G., Pace-Asciak C. R. Hepoxilin A3 induces changes in cytosolic calcium, intracellular pH and membrane potential in human neutrophils. Biochem J. 1990 Feb 15;266(1):63–68. doi: 10.1042/bj2660063. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. FILO R. S., BOHR D. F., RUEGG J. C. GLYCERINATED SKELETAL AND SMOOTH MUSCLE: CALCIUM AND MAGNESIUM DEPENDENCE. Science. 1965 Mar 26;147(3665):1581–1583. doi: 10.1126/science.147.3665.1581. [DOI] [PubMed] [Google Scholar]
  7. FURCHGOTT R. F., BHADRAKOM S. Reactions of strips of rabbit aorta to epinephrine, isopropylarterenol, sodium nitrite and other drugs. J Pharmacol Exp Ther. 1953 Jun;108(2):129–143. [PubMed] [Google Scholar]
  8. Forder J., Scriabine A., Rasmussen H. Plasma membrane calcium flux, protein kinase C activation and smooth muscle contraction. J Pharmacol Exp Ther. 1985 Nov;235(2):267–273. [PubMed] [Google Scholar]
  9. Godfraind T., Miller R. C., Lima J. S. Selective alpha 1- and alpha 2-adrenoceptor agonist-induced contractions and 45Ca fluxes in the rat isolated aorta. Br J Pharmacol. 1982 Dec;77(4):597–604. doi: 10.1111/j.1476-5381.1982.tb09337.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Greenwald J. E., Bianchine J. R., Wong L. K. The production of the arachidonate metabolite HETE in vascular tissue. Nature. 1979 Oct 18;281(5732):588–589. doi: 10.1038/281588a0. [DOI] [PubMed] [Google Scholar]
  11. Hokin L. E. Receptors and phosphoinositide-generated second messengers. Annu Rev Biochem. 1985;54:205–235. doi: 10.1146/annurev.bi.54.070185.001225. [DOI] [PubMed] [Google Scholar]
  12. Juchau M. R., Bond J. A., Benditt E. P. Aryl 4-monooxygenase and cytochrome P-450 in the aorta: possible role in atherosclerosis. Proc Natl Acad Sci U S A. 1976 Oct;73(10):3723–3725. doi: 10.1073/pnas.73.10.3723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kwan C. Y. Dysfunction of calcium handling by smooth muscle in hypertension. Can J Physiol Pharmacol. 1985 Apr;63(4):366–374. doi: 10.1139/y85-066. [DOI] [PubMed] [Google Scholar]
  14. Laneuville O., Corey E. J., Couture R., Pace-Asciak C. R. Hepoxilin A3 (HxA3) is formed by the rat aorta and is metabolized into HxA3-C, a glutathione conjugate. Biochim Biophys Acta. 1991 Jun 19;1084(1):60–68. doi: 10.1016/0005-2760(91)90056-n. [DOI] [PubMed] [Google Scholar]
  15. Laneuville O., Corey E. J., Couture R., Pace-Asciak C. R. Hepoxilin A3 increases vascular permeability in the rat skin. Eicosanoids. 1991;4(2):95–97. [PubMed] [Google Scholar]
  16. Larrue J., Rigaud M., Razaka G., Daret D., Demond-Henri J., Bricaud H. Formation of monohydroxyeicosatetraenoic acids from arachidonic acid by cultured rabbit aortic smooth muscle cells. Biochem Biophys Res Commun. 1983 Apr 15;112(1):242–249. doi: 10.1016/0006-291x(83)91822-3. [DOI] [PubMed] [Google Scholar]
  17. Masferrer J., Mullane K. M. Modulation of vascular tone by 12(R)-, but not 12(S)-, hydroxyeicosatetraenoic acid. Eur J Pharmacol. 1988 Jul 14;151(3):487–490. doi: 10.1016/0014-2999(88)90549-3. [DOI] [PubMed] [Google Scholar]
  18. Moncada S., Herman A. G., Higgs E. A., Vane J. R. Differential formation of prostacyclin (PGX or PGI2) by layers of the arterial wall. An explanation for the anti-thrombotic properties of vascular endothelium. Thromb Res. 1977 Sep;11(3):323–344. doi: 10.1016/0049-3848(77)90185-2. [DOI] [PubMed] [Google Scholar]
  19. Mulvany M. J., Aalkjaer C., Christensen J. Changes in noradrenaline sensitivity and morphology of arterial resistance vessels during development of high blood pressure in spontaneously hypertensive rats. Hypertension. 1980 Sep-Oct;2(5):664–671. doi: 10.1161/01.hyp.2.5.664. [DOI] [PubMed] [Google Scholar]
  20. Nigam S., Nodes S., Cichon G., Corey E. J., Pace-Asciak C. R. Receptor-mediated action of hepoxilin A3 releases diacylglycerol and arachidonic acid from human neutrophils. Biochem Biophys Res Commun. 1990 Sep 28;171(3):944–948. doi: 10.1016/0006-291x(90)90775-i. [DOI] [PubMed] [Google Scholar]
  21. Pace-Asciak C. R. Arachidonic acid epoxides. Demonstration through [18O]oxygen studies of an intramolecular transfer of the terminal hydroxyl group of (12S)-hydroperoxyeicosa-5,8,10,14-tetraenoic acid to form hydroxyepoxides. J Biol Chem. 1984 Jul 10;259(13):8332–8337. [PubMed] [Google Scholar]
  22. Pace-Asciak C. R., Granström E., Samuelsson B. Arachidonic acid epoxides. Isolation and structure of two hydroxy epoxide intermediates in the formation of 8,11,12- and 10,11,12-trihydroxyeicosatrienoic acids. J Biol Chem. 1983 Jun 10;258(11):6835–6840. [PubMed] [Google Scholar]
  23. Pace-Asciak C. R. Hemoglobin- and hemin-catalyzed transformation of 12L-hydroperoxy-5,8,10,14-eicosatetraenoic acid. Biochim Biophys Acta. 1984 May 11;793(3):485–488. doi: 10.1016/0005-2760(84)90267-4. [DOI] [PubMed] [Google Scholar]
  24. Pace-Asciak C. R., Martin J. M. Hepoxilin, a new family of insulin secretagogues formed by intact rat pancreatic islets. Prostaglandins Leukot Med. 1984 Nov;16(2):173–180. doi: 10.1016/0262-1746(84)90069-6. [DOI] [PubMed] [Google Scholar]
  25. Rasmussen H., Forder J., Kojima I., Scriabine A. TPA-induced contraction of isolated rabbit vascular smooth muscle. Biochem Biophys Res Commun. 1984 Jul 31;122(2):776–784. doi: 10.1016/s0006-291x(84)80101-1. [DOI] [PubMed] [Google Scholar]
  26. Shibata S., Kuchii M., Taniguchi T. Calcium flux and binding in the aortic smooth muscle from the spontaneously hypertensive rat. Blood Vessels. 1975;12(5):279–289. doi: 10.1159/000158063. [DOI] [PubMed] [Google Scholar]
  27. Weksler B. B., Marcus A. J., Jaffe E. A. Synthesis of prostaglandin I2 (prostacyclin) by cultured human and bovine endothelial cells. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3922–3926. doi: 10.1073/pnas.74.9.3922. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Winquist R. J., Bohr D. F. Structural and functional changes in cerebral arteries from spontaneously hypertensive rats. Hypertension. 1983 May-Jun;5(3):292–297. doi: 10.1161/01.hyp.5.3.292. [DOI] [PubMed] [Google Scholar]
  29. Zsotér T. T., Wolchinsky C., Henein N. F., Ho L. C. Calcium kinetics in the aorta of spontaneously hypertensive rats. Cardiovasc Res. 1977 Jul;11(4):353–357. doi: 10.1093/cvr/11.4.353. [DOI] [PubMed] [Google Scholar]

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