Skip to main content
Log in

Anti-inflammatory effect of warfarin and vitamin K1

  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Summary

  1. 1.

    Sodium warfarin, given by oral or by parenteral route, displays a pronounced antiinflammatory effect in the formaldehyde and carrageenan induced rat paw edema. This effect becomes patent not only when the warfarin application precedes the local injection of the irritant substance (prophylactic effect), but also when it is given to animals with already developed inflammatory reactions (therapeutic effect).

  2. 2.

    The active doses of Na warfarin lie between 0.5 and 5.0 mg/kg. Smaller as well as higher doses show a reduced anti-inflammatory effect.

  3. 3.

    A marked anti-inflammatory effect can be noted already 90 min after drug injection at a still normal prothrombin level.

  4. 4.

    Vitamin K1 (phylloquinone), given by oral or parenteral route, in doses from 1.6 mg/kg upwards, shows a marked anti-inflammatory effect both in the prophylactic and the therapeutic rat paw test. Vitamin K3 is devoid of any anti-inflammatory activity.

  5. 5.

    The anti-inflammatory effect of both sodium warfarin and of vitamin K1 in rats, is not interfered with by previous adrenalectomy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • van Arman, C. G., Begany, A. J., Miller, L. M., Pless, H. H.: Some details of the inflammations caused by yeast and carrageenin. J. Pharmacol. Exp. Ther. 150, 328–334 (1965)

    Google Scholar 

  • Berquó, E., Marques, R. M.: Analise de variância São Paulo: Cadeira de Estatística da Faculdade de Higiene e Saúde Pública 1964

    Google Scholar 

  • Brodie, A. F.: Vitamin K and other quinones as coenzymes in oxidative phosphorylation in bacterial systems. Fed. Proc. 20, 995–1004 (1961)

    Google Scholar 

  • D'Amour, F. E., Blood, F. R.: Manual for laboratory work in mammalian physiology. Chicago: The Univ. of Chicago Press 1961

    Google Scholar 

  • Eichbaum, F.: Extraanticoagulant effects of oral anticoagulants. Arq. Bras. Cardiol. 286, 637–641 (1975a)

    Google Scholar 

  • Eichbaum, F.: Anticoagulants and cancer, a review. Rev. Bras. Pesq. Med. e Biol. 85, 489–496 (1975b)

    Google Scholar 

  • Fontaine, L., Grand, M., Molho, D. Z., Boschetti, E.: Activit e antiinflammatoire expérimentale de coumarines, indane-diones et acyl-indane-diones apparentées aux anticoagulants oraux. Med. Pharmacol. Exp. 17, 497–507 (1967)

    Google Scholar 

  • Fontaine, L., Grand, M., Quintin, J., Merle, S.: Activité antiinflammatoire comparée de substances anticoagulantes. Mode d'action de la Phénylandanadione. Med. Pharmacol. Exp. 13, 137–154 (1965)

    Google Scholar 

  • Fontaine, L., Odievre, M., Cachet, J., Drevon, B.: Pharmacologie de la phenyl-indanedione. Therapie XVI, 34–50 (1961)

    Google Scholar 

  • Goldstein, A.: Biostatistics. New York: Macmillan 1967

    Google Scholar 

  • Link, K. P., Overman, R. S., Sullivan, W. H., Huebner, C. F., Sheel, L. D.: Studies on the haemorrhagic sweet clover disease. XI. Hypoproteinaemia in the rat induced by salicylic acid. J. Biol. Chem. 147, 463–474 (1943)

    Google Scholar 

  • Piller, N. B.: The resolution of thermal edema at various temperatures under coumarin treatment. Br. J. Exp. Pathol. 56, 83–91 (1975)

    Google Scholar 

  • Piller, N. B.: Drug induced proteolysis: a correlation with edema reducing ability. Br. J. Exp. Pathol. 57, 266–273 (1976a)

    Google Scholar 

  • Piller, N. B.: Comparison of the effect of benzopyrones and other drugs with anti-inflammatory properties on acid and neutral protease activity levels in various tissues after thermal injury. Br. J. Exp. Pathol. 57, 411–418 (1976b)

    Google Scholar 

  • Piller, N. B.: The action of benzopyrones on an experimental model of lymphedema: a contribution to their mode of action. Br. J. Exp. Pathol. 57, 713–721 (1976c)

    Google Scholar 

  • Piller, N. B.: Tissue levels of (3−14C) coumarin in the rat: distribution and excretion. Br. J. Exp. Pathol. 58, 28–34 (1977)

    Google Scholar 

  • Quick, A. J.: The physiologic pharmacology of homeostasis, pp. 125–134. New York: Lea and Febiger 1951

    Google Scholar 

  • v. Rechenberg, H. K. (ed.): Butazolidin, Phenylbutazon, pp. 32/33. Stuttgart: G. Thieme 1961

    Google Scholar 

  • Renk, E., Stoll, W. G.: Orale Antikoagulantien. Fortschr. Arzneimittelforsch. 11, 226–355 (1968)

    Google Scholar 

  • Thiers, H.: In. Les Vitamines, pp. 333–336. Paris: Masson 1956

    Google Scholar 

  • Weiner, M., Shapiro, S., Axelrod, J., Cooper, J. R., Brodie, B. B.: The physiological disposition of dicoumarol in man. J. Pharmacol. Exp. Ther. 99, 409–420 (1950)

    Google Scholar 

  • Wosilait, A. D.: Role of vitamin K in electron transport. Fed. Proc. 20, 1005–1011 (1961)

    Google Scholar 

  • Yacobi, A., Wingard, L. B. jr., Levy, G.: Comparative pharmacocinetics of coumarin anticoagulants. X. Relationship between distribution and anticoagulant action of warfarin. J. Pharm. Sci. 63, 868–872 (1974)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Eichbaum, F.W., Slemer, O. & Zyngier, S.B. Anti-inflammatory effect of warfarin and vitamin K1 . Naunyn-Schmiedeberg's Arch. Pharmacol. 307, 185–190 (1979). https://doi.org/10.1007/BF00498462

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00498462

Key words

Navigation