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2005 | 57 | 1 |

Tytuł artykułu

Oddzialywanie przeciwwirusowe oraz cytotoksycznosc nowych pochodnych naturalnych seskwiterpenow i taksolu

Warianty tytułu

EN
Antiviral and cytotoxic activities of new derivatives of natural sesquiterpenes and taxol

Języki publikacji

PL

Abstrakty

PL
W badaniach prowadzonych uprzednio w Katedrze i Zakładzie Mikrobiologii Lekarskiej stwierdzono, że niektóre pochodne naturalnych seskwiterpenów oraz taksolu wykazywały aktywność przeciwwirusową, hamując namnażanie wirusa HSV-1 in vitro. Celem niniejszej pracy było uzyskanie wglądu w przeciwwirusową i przeciwbakteryjną aktywność siedmiu nowo zsyntety- zowanych związków chemicznych tej grupy.
EN
Common occurrences of serious viral infections and a small number of available antiviral chemotherapeutics necessitate research for new, biologically active substances, which might be of use as antiviral drugs. Natural compounds, e.g., derived from plants and fungi, which show significant and various biological activities, may be a source of potential drugs. Sesquiterpenes, as well as taxol, and their derivatives, may serve as an example. The aim of the present study was to investigate the antiviral, antibacterial and cytotoxic properties of 7 new compounds: derivatives of sesquiterpenes of Lactarius mushroom origin and taxol - JV-benzoylphenylisoserinates of sesquiterpenoid alcohols. The cytotoxicity of the tested compounds against Vero, RD, LLC-MK2 and AJ49 cell lines were assessed using the formazan method. All compounds showed a lower cytotoxicity than taxol. Their antiviral activity in vitro was evaluated by assessing the reduction of virus titre in cells subjected to the compounds in comparison to the cells, which were not subjected to them. It was found that out of 7 investigated compounds 3 exhibited antiviral activity. These compounds inhibited replication of HSV-1 virus in Vero cells. It appears therefore that further investigation of these groups of compounds and their derivatives is justified because they may constitute a potential source of chemotherapeutics.

Wydawca

-

Rocznik

Tom

57

Numer

1

Opis fizyczny

s.93-99,rys.,tab.,bibliogr.

Twórcy

autor
  • Akademia Medyczna w Warszawie, ul.T.Chalubinskiego 5, 02-004 Warszawa
autor
autor

Bibliografia

  • 1. Anke H, Bergendorff O, Sterner O. Assays of the biological activities of guaiane sesquiterpenoids isolated from the fruit bodies of edible Lactarius species. Food Chem Toxicol 1989; 27: 393-7.
  • 2. Daniewski WM, Gumulka M, Przesmycka D i inni. Sesquiterpenes of Lactarius origin, antifeedant structure - activity reletionships. Phytochemisty 1995; 38: 1161-8.
  • 3. Daniewski WM, Vidari G. Constituents of Lactarius (Mushrooms). W: Progress in the Chemistry of Organic Natural Products. Red. W. Herz, H. Falk, G.W. Kirby, R.E. Moore, C. Tamm, Springer-Verlag Wien New York 1999, 70-171.
  • 4. Doljak B, Stegnar M, Urleb U i inni. Screening for selective thrombin inhibitors in mushrooms. Blood Coagul Fibrinolysis 2001; 12: 123-8.
  • 5. Garlashelli L, Mellerio G, Vidari G, Vita-Finzi P. New fatty acid esters of drimane sesquiterpenes from Lactarius uvidus. J Nat Prod 1994; 57: 905-10.
  • 6. Jassim SA, Naji MA. Novel antiviral agents: a medicinal plant perspective. J Appl Microbiol 2003; 95: 412-27.
  • 7. Kim SE, Kim YH, Kim YC, Lee JJ. Torilin, a sesquiterpene from Torilis japonica, reverses multi resistance in cancer cells. Planta Med 1998; 64: 332-4.
  • 8. Kobus M, Krawczyk E, Kopczacki P i inni. Wpływ nowo zsyntetyzowanych seskwiterpenowych analogów taksolu na namnażanie wirusa opryszczki (HSV-1MC) oraz retrowirusa (Mo-MSV). Med Dośw Mikrobiol 2001; 53: 282-9.
  • 9. Kobus M, Łuczak M, Krawczyk E i inni. Effect of 5,10a,13-trihydroxy-2α,9α-H-marasm-7(8)-en on experimental Herpes simplex virus type 1 infections (in vitro and in vivo). W. Chemotherapy, 12th Mediterranean Congress of Chemotherapy. Red. H. Himmich, Monduzzi Editore S.p. A., International Proceedings Division, 2000, 141-7.
  • 10. Kopczacki P, Gumulka M, Masnyk M i inni. Synthesis and antifeedant properties of N-benzoylphenylisoserinates of Lactarius sesquiterpenoid alcohols. Phytochemistry 2001; 58: 775-87.
  • 11. Krawczyk E, Łuczak M, Kobus M, Bańka D, Daniewski W. Antiviral activity of N-benzoylphenylisoserinates of Lactarius sesquiterpenoid alcohols. Planta Med 2003; 69: 552-4.
  • 12. Mayer AM, Hamann MT. Marine pharmacology in 1999: compounds with antibacterial, anticoagulant, antifungal, antihelmintic, anti-inflammatory, antiplatelet, antiprotozoal and antiviral activities affecting the cardiovascular, endocrine, immune and nervous systems, and other miscellaneous mechanisms of action
  • 13. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Meth 1983; 65: 55-63.
  • 14. Patel NM, Nozaki S, Shortle NH i inni. Paclitaxel sensitivity of breast cancer cells with constitutively active NF-kB is enhanced by ІкВа super-repressor and parthenolide. Oncogene 2000; 19: 4159-69.
  • 15. Reed ŁJ, Muench MA. A simple method of estimating fifty percent end points. Am J Hyg 1938; 27: 493-87.
  • 16. Sivropoulou A, Nikolaou C, Papanikolaou E i inni. Antimicrobial, cytotoxic and antiviral activities of Salvia fructicosa essential oil. J Agric Food Chem 1997; 45: 3197-201.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-98274831-ed30-4220-91f2-dc0ad3ffb8f0
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