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1991 | 42 | 2 |

Tytuł artykułu

Role of polyamines in gastroprotection induced by epidermal growth factor

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Polyamines have been shown to stimulate cellular growth and differentiation, though their role in the prevention of acute gastric lesion induced by various noxious agents has been little studied. Epidermal growth factor (EGF) exhibits gastroprotective and ulcer healing properties due to its potent mitogenic and growth promoting action. This study was designed to compare the gastroprotective effects of spermine and EGF against gastric damage induced by absolute ethanol, acidified aspirin and stress and to determine the role of endogenous polyamines in EGF-induced gast- troprotection. Spermine and EGF significantly reduced the lesions induced by all three ulcerogens. Oral administration of spermine or subcutaneous infusion of EGF in 24 h fasted rats with chronic gastric fistula resulted in similar inhibition of gastric acid and pepsin secretion. Pretreatment with difluoromethylornithine (DFMO), an irreversible inhibitor of ornithine decarboxylase (ODC), a hey enzyme in the biosynthesis of polyamines, did not affect ethanol lesions, but reversed the protective effect EGF but not spermine, against ethanol. This finding indicates that polyamines mediate, at least in part, EGF-induced gastroprotection. In tests with oral administration of aminoguanidine that is known to suppress the activity of diamino-oxidase (DAO) and to inhibit the degradation of polyamines, EGF showed a markedly enhanced gastroprotective activity against ethanol damage. Since indomethacin failed to affect the gastroprotective effects of spermine and EOF and neither of these agents influenced the mucosal generation of PGE₂ in intact or injured gastric mucosa, we conclude that prostaglandins are not the major factors in spermine- and EGF-induced gastroprotection. This study demonstrates that polyamines are highly effective against gastric lesions induced by various ulcerogens and that they act as primary mediators of EGF-induced gastroprotection.

Wydawca

-

Rocznik

Tom

42

Numer

2

Opis fizyczny

p.181-193,fig.,ref.

Twórcy

  • Institute of Physiology, Academy of Medicine, Grzgorzecka 16, 31-531 Krakow, Poland
  • Institute of Physiology, Academy of Medicine, Grzgorzecka 16, 31-531 Krakow, Poland
autor
  • Institute of Physiology, Academy of Medicine, Grzgorzecka 16, 31-531 Krakow, Poland
  • Institute of Physiology, Academy of Medicine, Grzgorzecka 16, 31-531 Krakow, Poland
  • Institute of Physiology, Academy of Medicine, Grzgorzecka 16, 31-531 Krakow, Poland

Bibliografia

  • 1. Williams-Ashman HG, Canellakis ZN. Polyamines in mammalian biology and medicine. Perspect Biol Med 1979; 22: 241-453.
  • 2. Pegg AE, Mc Саnn PP. Polyamine metabolism and function. Am J Physiol 1982; 243: C212-C221.
  • 3. Tabor CW, Tabor H. Polyamines in microorganisms. Microbiol Rev 1985; 49: 81-99.
  • 4. Ginty DD, Scidel ER. Polyamine - dependent growth and calmodulin - regulated induction of ornithine decarboxylase. Am J Physiol 1989; 256: G342-G349.
  • 5. Ginty DD, Osborne DL, Scidel ER. Putrescine stimulates DNA synthesis in intestinal epithelial cells. Am J Physiol 1989; 257: G145-G150.
  • 6. Carpenter G, Cohen S. Epidermal growth factor. Ann Rev Biochem 1979; 48: 193- 216.
  • 7. Konturek SJ, Brzozowski T, Piastucki I, et al. Role of mucosal prostaglandins and DNA synthesis in gastric cytoprotection by luminal epidermal growth factor. GUT 1981; 22: 927-932.
  • 8. Konturek SJ, Radecki T, Brzozowski T, et al. Gastric protection by epidermal growth factor. Role of endogenous prostaglandins and DNA synthesis. Gastroenterology 1981; 81: 438-443.
  • 9. Dembiński A, Gregory H, Konturek SJ, Polanski M. Trophic action of epidermal growth factor on the pancreas and gastroduodenal mucosa in rats. J Physiol (London) 1982, 325; 35: 35-42.
  • 10. Feldman EJ, Aures D, Grossman MI. Epidermal growth factor stimulates ornithine decarboxylase activity in the digestive tract of mouse. Proc Soc Exp Biol Med 1978; 159: 400-402.
  • 11. Takagi K, Kasuya Y, Watanabe K. Studies on the drugs for peptic ulcer: a reliable method for producing stress ulcers in rats. Chem Pharm Bull 1964; 12: 465-470.
  • 12. Ray TK, Nandi J, Pidhorodeckyi N, Meng-Ai Z. Polyamines are inhibitors of gastric acid secretion. Proc Natl Acad Sci 1982; 79: 1448-1452.
  • 13. Kozol R, Fromm D, Ray TK. Effect of a naturally occuring polyamine on acid secretion by isolated gastric mucosa. Proc Soc Exp Biol Med 1984; 175: 62-57.
  • 14. Nandi J, Wright MV, Fromm D, Ray TK. Oral administration of spermine inhibits gastric acid secretion in rats. Dig Dis Sci 1983; 28: 513-517.
  • 15. Aihara H, Otomo S, Isobe Y, Ohzeki M, Igarashi K, Hirose S. Polyamine inhibition of gastric ulceration in rats. Biochem Pharmacol 1983; 32: 1733-1736.
  • 16. Konturek SJ, Brzozowski T, Dembiński A, Warzecha Z, Yamazaki J. Gastric protective and ulcer healing action of epidermal growth factor. In Advances in Drug Therapy of Gastrointestinal Ulceration, A. Garner & В JR Whittle (eds.) Chichester, Wiley and Sons Ltd, 1989, pp 261-272.
  • 17. Mizui T, Shimono N, Doteuchi M. A possible mechanisms of protection by polyamines against gastric damage induced by acidified ethanol in rats: poly amine protection may depend on its antiperoxidative properties. Japan J Pharmacol 1987; 44: 43-50.
  • 18. Skov Olsen P, Poulsen SS, Kirkegaard P, Nexo E. Role submandibular saliva and epidermal growth factor in gastric cytoprotection. Gastroenterology 1984; 87: 103-108.
  • 19. Konturek SJ, Dembinski A, Warzecha Z, Brzozowski T, Gregory H. Role of epidermal growth factor in healing of chronic gastroduodenal ulcers in rats. Gastroenterology 1988; 94: 1300-1307.
  • 20. Brzozowski T, Konturek SJ, Drozdowicz D, Warzecha Z, Yanaihara N. Epidermal growth factor in the ulcer healing action of colloidal bismuth subcitrate (DeNol) in rats. Eur J Gastroenterol Hepatol 1989; 1: 117-124.
  • 21. Skov Olsen P, Poulsen SS, Thekelsen K, Nexo E. Effect of sialoadenectomy and synthetic human urogastrone on healing of chronic gastric ulcers in rats. Gut 1987; 27: 1443-1449.
  • 22. Skinner KA, Soper BD, Tepperman BL. Effect of sialoadenectomy and salivary gland extracts on gastric mucosal growth and gastric levels in the rat. J Physiol (London) 1984; 351: 1-12.
  • 23. Skinner KA, Tepperman BL. Influence of desalivation on acid secretory output and gastric mucosal integrity in the rat. Gastroenterology 1981; 81: 335-339.
  • 24. Tepperman BL, Soper BD, Morris GP. Effect of sialoadenectomy on adaptive cytoprotection in the rat. Gastroenterology 1989; 97: 123-129.
  • 25. Osborne DL, Seidel ER. Gastrointestinal luminal polyamines: cellular accumulation and enterohepatic circulation. Am J Physiol 1990; 258: G576-G584.
  • 26. Baylin SB, Stevens SA, Shakim KM. Association of diamino oxidase and ornithin decarboxylase with maturating cells in rapidly proliferating epithelium. Biochim Biophys Acta 1978; 541: 415-419.
  • 27. Luk GD, Marton LJ, Baylin SB. Ornithine decarboxylase is important in intestinal mucosal maturation and recovery from injury in rats. Science 1980; 210: 195-198.
  • 28. Furihata C, Sata Y, Hosaka M, Matsushima T, Furukawa F, Takahashi M. NaCl- -induced ornithine decarboxylase activity and DNA synthesis in rat stomach mucosa. Biochem Biophys Res Commun 1984; 121: 1027-1032.
  • 29. Thirumalai Ch, Tseng CW, Tabata K, Fitzpatrick L, Johnson LR. Relationship between ornithine decarboxylase activity and gastric damage. Am J Physiol 1987 ; 253: Gl-G6.
  • 30. Wang J-Y, Johnson LR. Induction of gastric and duodenal mucosal ornithine decarboxylase during stress. Am J Physiol 1989; 257: G259-G266.
  • 31. Konturek PK, Brzozowski T, Konturek SJ, Dembinski A. Role of epidermal growth factor, prostaglandin and sulfhydryls in stress-induced gastric lesions. Gastroenterology 1990; 99: 1607-1615.
  • 32. Hosomi M, Stace NH, Lirussi F, Smith SM, Murphy GM, Dowling RH. Role of polyamines in intestinal adaptation in the rat. Eur J Clin Invest 1987; 17: 375-385.
  • 33. Luk GD, Baylin SB. Polyamines and intestinal growth: increased polyamine biosynthesis after jejunectomy. Am J Physiol 1983; 245: G656-G660.
  • 34. Konturek SJ, Brzozowski T, Piastucki I, Radecki T, Dembiński A, Dembinska-Kiec A. Role of locally generated prostaglandins in adaptive cytoprotection. Dis Dis Sci 1982; 27: 967-971.
  • 35. Hiraishi H, Terano A, Ohta S. et al. Epidermal growth factor protects rat gastric mucosal cells against indomethacin - induced damage in monolayer culture. Gastroentrology 1984; 86: A1113.
  • 36. Chiba T, Hirata Y, Taminato T, Kadowski S, Matsukara S, Fujita T. Epidermal growth factor stimulates prostaglandin E₂ release from isolated rat stomach. Biochem Biophys Res Commun 1982; 105: 370-374.

Typ dokumentu

Bibliografia

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