Skip to main content
Log in

Studies on Anti-Inflammatory Action of Tryptanthrin, Using a Model of DSS-Induced Colitis of Mice and Magnetic Resonance Imaging

  • Published:
Applied Magnetic Resonance Aims and scope Submit manuscript

Abstract

The action of tryptanthrin, a known natural alkaloid, a potent inhibitor of cyclooxygenase COX-2 and 5-lipoxygenase, was studied in a model of dextran sodium sulfate (DSS)-induced mouse colitis by magnetic resonance imaging (MRI). It was shown that the intra-ventricular treatment with tryptanthrin suspensions or emulsion at a dose of 25 mg/kg effectively diminishes lethality at experimental groups and normalizes morphometric parameters of intestine in the treated animals. MR imaging confirmed anti-inflammatory effect of this alkaloid and its capability to decrease the size of bowel walls in animals with colitis.

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.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. E. Von Sommaruga, Justis Libiegs Ann. der Chemie. 195, 302–313 (1879)

    Article  Google Scholar 

  2. P. Friedlander, N. Roschdestwensky, Chem. Ber. 48, 1841–1847 (1915)

    Article  Google Scholar 

  3. F. Schindler, H. Zahner, Arch. Mikrobiol. 79, 187–203 (1971)

    Article  Google Scholar 

  4. A. Sen, S. Mahato, N. Dutta, Tetrahedron Lett. 15, 609–610 (1974)

    Article  Google Scholar 

  5. J. Bergman, B. Egestad, J.O. Lindstrom, Tetrahedron Lett. 18, 2625–2626 (1977)

    Article  Google Scholar 

  6. T. Hosoe, K. Nosawa, N. Kawahara, K. Fukushima, K. Nishimura, M. Miyaji, K. Kawai, Mycopathologia 146, 9–12 (1999)

    Article  Google Scholar 

  7. I. Wagner-Dobler, H. Rheims, A. Felske, A. El-Ghezal, D. Flade-Schroder, H. Laatsch, S. Lang, R. Pukall, B.J. Tindall, Int. J. Syst. Evol. Microbiol. 54, 1177–1179 (2004)

    Article  Google Scholar 

  8. G. Honda, V. Tosirisuk, M. Tabata, Planta Med. 38, 275–276 (1980)

    Article  Google Scholar 

  9. H. Danz, D. Baumann, M. Hamburger, Planta Med. 68, 152–157 (2002)

    Article  Google Scholar 

  10. H. Danz, S. Stoyanova, P. Wippich, A. Brattstrom, M. Hamburger, Planta Med. 67, 411–416 (2001)

    Article  Google Scholar 

  11. V. George, A.S. Koshy, O.V. Singh, M.N.S. Nayar, P. Pushpangadan, Fitoterapia 67, 553–554 (1996)

    Google Scholar 

  12. A.V. Muruganandam, S.K. Bhattacharya, Ind. J. Chem.-Sect. B 39B, 125-131 (2000)

  13. G. Honda, M. Tabata, Planta Med. 36, 85–86 (1979)

    Article  Google Scholar 

  14. M. Yoshikawa, T. Muracami, A. Kishi, T. Sakurama, H. Matsuda, M. Nomura, H. Matsuda, M. Kubo, Chem. Pharm. Bull. 46, 886–888 (1998)

    Article  Google Scholar 

  15. T. Murakami, A. Kishi, T. Sacurama, H. Matsuda, M. Yoshicawa, Heterocycles 54, 957–966 (2001)

    Article  Google Scholar 

  16. J. Bergman, J. Lindstroem, U. Tilstam, Tetrahedron 41, 2879–2881 (1985)

    Article  Google Scholar 

  17. Y. Jahng, Arch. Pharm. Res. 36, 517–535 (2013)

    Article  Google Scholar 

  18. A. Tucker, P. Grundt, Arkivoc. (i) 546-569 (2012)

  19. T. Moskovkina, A. Kalinovskii, V. Makhan’kov, Russ. J. Org. Chem. 48, 123–126 (2012)

    Article  Google Scholar 

  20. T. Moskovkina, M. Denisenko, A. Kalinovskii, V. Stonik, Russ. J. Org. Chem. 49, 1740–1743 (2013)

    Article  Google Scholar 

  21. G. Honda, M. Tabeta, M. Tsuda, Planta Med. 37, 172–174 (1979)

    Article  Google Scholar 

  22. P. Bandekar, K. Roopnarine, V. Parekh, T. Mitchell, M. Novak, R. Sinden, J. Med. Chem. 53, 3558–3565 (2010)

    Article  Google Scholar 

  23. W. Baker, L. Mitscher, U.S. Patent 5, 441, 955 (1995)

  24. L. Mitscher, W. Baker, Med. Res. Rev. 18, 363–374 (1998)

    Article  Google Scholar 

  25. M. Kataoka, K. Hirata, T. Kunikata, S. Ushio, K. Iwaki, K. Ohashi, M. Ikeda, M. Kurimoto, J. Gastroenterol. 36, 5–9 (2001)

    Article  Google Scholar 

  26. A. Bhattacharjee, D. Skanchy, B. Jennings, T. Hudson, J. Brendle, K. Werbovetz, Bioorg. Med. Chem. 10, 1979–1989 (2004)

    Article  Google Scholar 

  27. K. Pitzer, J. Scovill, D. Kyle, L. Gerena. US Patent, 6,531,487 (2003)

  28. J. Scovill, E. Blank, M. Konnick, E. Nenortas, T. Shapiro, Antimicr. Agents Chemotherap. 46, 882–883 (2002)

    Article  Google Scholar 

  29. H. Chan, H. Yip, N. Mak, K. Leung, Cell. Molecul. Immunol. 6, 335–342 (2009)

    Article  Google Scholar 

  30. C. Oberthuer, R. Jaeggi, M. Hamburger, Fitoterapia 76, 324–332 (2005)

    Article  Google Scholar 

  31. M. Micallef, K. Iwaki, T. Ishihara, S. Ushio, M. Aga, T. Kunikata, S. Koya-Miayata, T. Kimoto, M. Ikeda, M. Kurimoto, Int. Immunopharmacol. 2, 565–578 (2002)

    Article  Google Scholar 

  32. T. Ishihara, K. Kohno, S. Ushio, K. Iwaki, M. Ikeda, M. Kurimoto, Eur. J. Pharmacol. 407, 197–204 (2000)

    Article  Google Scholar 

  33. J. Terrah, P. Olson, R. Halberg, Experimental Small Animal Colonoscopy. ed. P. Misouitz, Medicine/Gasteroenterology/Colonoscopy. 297 p. (2007) doi:10.5772/21573

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Irina G. Agafonova.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Agafonova, I.G., Moskovkina, T.V. Studies on Anti-Inflammatory Action of Tryptanthrin, Using a Model of DSS-Induced Colitis of Mice and Magnetic Resonance Imaging. Appl Magn Reson 46, 781–791 (2015). https://doi.org/10.1007/s00723-015-0674-3

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00723-015-0674-3

Keywords

Navigation