Skip to main content
Log in

Antiangiogenic effect of sulphated and nonsulphated glycosaminoglycans and polysaccharides in the chick embryo chorioallantoic membrane

  • Papers
  • Published:
Glycoconjugate Journal Aims and scope Submit manuscript

Abstract

The inhibiting effect of sulphated and nonsulphated glycosaminoglycans and polysaccharides on the normal outgrowth of capillaries was tested in the chick embryo chorioallantoic membrane (CAM) with and without the presence of hydrocortisone. An antiangiogenic response to 50 µg of heparin and heparan sulphate (without hydrocortisone present) was observed in 38.8% and 23.1% of the CAMS, respectively, while the antiangiogenic response rate for dermatan sulphate, chondroitin sulphate A or C, hyaluronic acid and keratan sulphate was 15.9–0%. All sulphated homopolysaccharides tested were more effective than the naturally occurring glycosaminoglycans. Nonsulphated dextran and (methyl) cellulose had no antiangiogenic effect, while largely desulphated heparin retained such an effect. Hydrocortisone generally improved the antiangiogenic effect, a 100% response was obtained when it was combined with cellulose sulphate or fucoidan (polyfucose sulphate derived from marine algae), but the antiangiogenic effect of the largely desulphated heparin was unaffected by the presence of hydrocortisone. The results show that different polysulphated polysaccharides also have an antiangiogenic effect, without the addition of corticosteroids. The effect was apparently independent of their degree of sulphation, but the glycosidic structure may be of critical importance.

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

  1. Folkman J, Klagsbrun M (1987)Science 235:442–7.

    Google Scholar 

  2. Thornton SC, Mueller SN, Levine EM (1983)Science 222:623–25.

    Google Scholar 

  3. Azizkhan RG, Azizkhan JC, Zetter BR, Folkman J (1980)J Exp Med 152:931–44.

    Google Scholar 

  4. Taylor S, Folkman, J (1982)Nature 297:307–12.

    Google Scholar 

  5. Sakamoto N, Tanaka NG, Tohgo A, Osada Y, Ogawa H (1987)J Natl Cancer Inst 78:581–5.

    Google Scholar 

  6. Folkman J, Langer R, Linhardt RJ, Haudenschild C, Taylor S (1983)Science 221:719–25.

    Google Scholar 

  7. Jakobson ÅM, Hahnenberger RW (1991)Pharmacol Toxicol (in press)

  8. Jakobson ÅM, Hahnenberger RW, Magnusson A (1989)Pharmacol Toxicol 6:193–5.

    Google Scholar 

  9. Crum R, Szabo S, Folkman J (1985)Science 230:1375–8.

    Google Scholar 

  10. Jacobsson I, Bäckström G, Höök M, Lindahl U, Feingold DS, Malmström A, Rodén L (1979)J Biol Chem 254:2975–82.

    Google Scholar 

  11. Maragoudakis ME, Sarmonika M, Panoutsacopoulou M (1989)J Pharm Exp Therap 251:679–82.

    Google Scholar 

  12. Ingber DE, Madri JA, Folkman J (1986)Endocrinology 119:1768–75.

    Google Scholar 

  13. Sakamoto N, Tanaka NG, Tohgo A, Osada Y, Ogawa H (1987)J Natl Cancer Inst 78:581–5.

    Google Scholar 

  14. Sakamoto N, Tanaka NG (1988)Cancer J 2:9–13.

    Google Scholar 

  15. Inoue K, Korenaga H, Tanaka NG, Sakamoto N, Kadoya S (1988)Carbohydr Res 181:135–42.

    Google Scholar 

  16. Folkman J, Weisz PB, Joullié MM, Li WW, Ewing WR (1989)Science 243:1490–3.

    Google Scholar 

  17. Herbert JM, Cottineau M, Driot F, Pereillo JM, Maffrand JP (1988)Biochem Pharmacol 37:4281–8.

    Google Scholar 

  18. Marcum AJ, Rosenberg RD (1989)Ann N Y Acad Sci 556:81–4.

    Google Scholar 

  19. Vlodavsky I, Eldor A, Bar-Ner M, Fridman R, Cohen IR, Klagsbrun M (1988)Adv Exp Med Biol 233:201–10.

    Google Scholar 

  20. Mizumoto K, Sugawara I, Ito W, Kodama T, Hayami M, Mori S (1988)Japan J Exp Med 58:145–51.

    Google Scholar 

  21. Baba M, Snoeck R, Pauwels R, De Clercq E (1988)Antimicrob Agents Chemother 32:1742–5.

    Google Scholar 

  22. Willenborg DO, Parish CR (1988)J Immunol 140:3401–5.

    Google Scholar 

  23. Dravland JE, Mortimer D (1988)Gamete Res 21:353–8.

    Google Scholar 

  24. Boldt J, Howe AM, Parkerson JB, Gunter LE, Kuehn E (1989)Biol Reprod 40:887–96.

    Google Scholar 

  25. Parish CR, Coombe DR, Jakobsen KB, Bennett FA, Underwood PA (1987)Int J Cancer 40:511–8.

    Google Scholar 

  26. Sugawara I, Ishizaka S (1982)Cell Immunol 68:402–9.

    Google Scholar 

  27. Sugawara I, Ishizaka S (1984)Microbiol Immunol 28:831–9.

    Google Scholar 

  28. Glabe CG, Yednock T, Rosen SD (1983)J Cell Sci 61:475–90.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hahnenberger, R., Jakobson, Å.M. Antiangiogenic effect of sulphated and nonsulphated glycosaminoglycans and polysaccharides in the chick embryo chorioallantoic membrane. Glycoconjugate J 8, 350–353 (1991). https://doi.org/10.1007/BF00731347

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00731347

Keywords

Navigation