PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2007 | 63 | 05 |

Tytuł artykułu

Effects of adenosine receptor agonists and antagonists on cytochrome P450 extinction in the liver of rats in the course of acute pancreatitis

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
In the course of acute pancreatitis the liver is an organ that is especially exposed to damage. The presence of adenosine receptors was observed in the whole digestive system. The aim of the experiment was to define the correlation between the extinction of cytochrome P450 in the liver of rats and adenosine receptor agonists and antagonists in the course of necrotizing acute pancreatitis. The experiments were carried out on Wistar male rats weighing 250 g. Acute pancreatitis was induced injecting 5% sodium taurocholate to the biliary-pancreatic duct. Prior to the induction of acute pancreatitis the animals were injected intraperitoneally with selective agonists and antagonists: CGS 21680 (selective A2 agonist), 3 mg/kg, ZM 241385 (selective A2a antagonist), 3 mg/kg, DPCPX (A1 antagonist), 1 mg/kg, 1.3-Dipropyl-8-phenylxantine (selective A1 antagonist), 3 mg/kg, IB-MECA (A3 agonist), 0.75 mg/kg. The determinations were performed in hepatic microsomes obtained according to Guegenrichs method Cytochrome P450 extinction was determined by Matsubars technique. The results obtained reveal statistically significantly decreased cytochrome P450 extinction after sodium taurocholate administration. Decreased levels of extinction were also observed after combined administration of sodium taurocholate + Phenylxantine and sodium taurocholate + ZM. The level of IB-MECA remained unchanged in comparison to the controls. However DPCPX and CGS administration increased the extinction of cytochrome P450. The diverse influence of adenosine receptor agonists and antagonists used in the experiment on cytochrom P450 extinction seems to modify the course of the inflammatory process after using 5% sodium taurocholate.

Wydawca

-

Rocznik

Tom

63

Numer

05

Opis fizyczny

p.528-531,ref.

Twórcy

autor
  • Medical University, Jaczewski Street 8, 20-954 Lublin, Poland
autor
autor
autor
autor
autor
autor

Bibliografia

  • 1.Acheson D. W., Rose P., Houston J. B., Braganza J. M.: Induction of cytochromes P-450 in pancreatic disease: consequence, coincidence or cause? Clin. Chim. Acta. 1985, 153, 73-84.
  • 2.Aho H. J., Koskensalo S. M., Nevalainen T. J.: Experimental pancreatitis in the rat. Sodium taurocholate-induced acute haemorrhagic pancreatits. Scand. J. Gastroenterol. 1980, 15, 411-416.
  • 3.Aho H. J., Nevalainen T. J., Aho A. J.: Experimental pancreatitis in the rat. Development of pancreatic necrosis, ischaemia and edema after intraductal sodium taurocholate infection. Eur. Surg. Res. 1983, 15, 28-36.
  • 4.Andrzejewska A.: Dynamika zmian morfologicznych w wątrobie w przebiegu ostrego zapalenia trzustki. Rozprawa habilitacyjna, AM Białystok 1990.
  • 5.Atamaca M., Fry J. R.: Adenosine-mediated inhibiton of glutathione synthesis in rat isolated hepatocytes. Biochem. Pharmacol. 1996, 52, 1423-1428.
  • 6.Day Y. J., Marshall M. A., Huang L., McDuffie M. J., Okusa M. D., Linden J.: Protection from ischaemic liver injury by activation of A2A adenosine receptors during reperfusion: inhibition of chemokine induction. Am. J. Physiol. Gastrointest. Liver. Physiol. 2004, 286, 285-293.
  • 7.Gomez G., Sitkovsky M. V.: Differential requirement for A2a and A3 adenosine receptors for the protective effect of inosine in vivo. Blood 2003, 102, 4472- -4478.
  • 8.Guegenrich F. P.: Microsomal enzymes involved in toxicology analysis and separation. Principles and Methods of Toxicology. Edited by A. Wallace Hayes. Raven Press, New York 1982.
  • 9.Inoue S., Kasihimoto W., Nakao A.: Anti-neutophil antibody attenuates the severity of acute lung injury in rats with experimental acute pancreatitis. Arch. Surgery 1995, 130, 93-98.
  • 10.Iwatsuki K., Yamagishi F., Homma N., Haruta K., Chiba S.: Blocking effects of verapamil on pancreatic exocrine secretion induced by dopamine in the dog. Arch. Int. Pharmacodyn. Ther. 1986, 280, 145-152.
  • 11.Kitamura O., Ozawa K., Honjo J.: Alterations of liver metabolism associated with experimental acute pancreatits. Am. J. Surg. 1973, 126, 379-382.
  • 12.Luthen R., Niderau C., Ferell L. D., Greendell J. H.: Intrapancreatic zymogen activation and levels of ATP and glutathione during caerulein pancreatitis in rats. Am. J. Physiol. 1995, 268, 592-604.
  • 13.Lutz W.: Mikrosomalne cytochromy P-450 komórek wątrobowych a ksenobiotyki przemysłowe i środowiskowe. Post. Hig. Med. Dośw. 1984, 38, 451-473.
  • 14.Matsubara T., Koike M., Touchi A., Tochino Y., Sugeno K.: Quantitative determination of cytochrome P-450 in rat liver homogenate. Analytical Biochemistry 1976, 75, 596-603.
  • 15.Nagy L. E.: Role of adenosine A1 receptors in inhibition of receptor-stimulated cyclic AMP production by ethanol in hepatocytes. Biochem. Pharmacol. 1994, 29, 2091-2096.
  • 16.Prokop;eva N. V., Guliaeva L. F., Poliakowa N. E.: Changes in the microsomal monooxygenase system of the rat liver in acute pancreatitis and during induction by Aroclor 1254. Biomed. Khim. 2004, 50, 52-56. (In Russian with English abstract).
  • 17.Satoh A., Satoh K., Masamune A., Yamagiva T., Shimosegawa T.: Activation of adenosine A2a receptor pathway reduces leukocyte infiltration but anhances edema formation in rat caerulein pancreatitis. Pancreas 2002, 24, 75-82.
  • 18.Satoh A., Shimosegawa T., Satoh K., Ito H., Kohno Y., Masamune A., Fujita M., Toyota T.: Activation of adenosine A1-receptor pathway induces edema formation in the pancreas of rats. Gastroenterol. 2000, 119, 829-836.
  • 19.Schultz H. U., Niederau C., Klonowski-Stumpe H., Halangk W., Luthen R., Lippert H.: Oxidative stress in acute pancreatitis. Hepatogastroenterology 1999, 46, 2736-2750.
  • 20.Smith S. R., Denhardt G., Terminelli C.: A role for histamine in cytokine modulation by the adenosine receptor agonist, 2-CI-IB-MECA. Eur. J. Pharmacol. 2002, 457, 57-69.
  • 21.Van Calker D., Muller M., Hamprecht B.: Adenosine inhibits the accumulation of cyclic AMP in cultured cells brain. Nature (London) 1978, 276, 839-841.
  • 22.Zhao A. Q., Nakamura M., Wang N. P., Wilcox S. N., Shearer S., Grytan R. A., Vinten-Johansen J.: Administration of adenosine during reperfusion reduces injury of vascular endothelium and death of myocytes. Coron. Arthery Dis. 1999, 10, 617-628.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-06c2c0a0-7a04-445f-8ae0-aa830795c774
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.