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1992 | 43 | 4 |

Tytuł artykułu

Direct protective action of epidermal growth factor on isolated gastric mucosal surface epithelial cells

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Epidermal growth factor (EGF) protects gastric mucosa against acute injury produced by a variety of damaging agents, but the mechanism of its protective action is not clear. Since the surface epithelial cells (SEC) are important component of gastric mucosal defence, we studied whether EGF may directly protect isolated gastric SEC against ethanol injury in vitro, in condition independent of systemic factors and whether endogenous prostaglandins may play a role in EGF’s protective action. The isolated SEC from rat gastric mucosa were preincubated in medium only, or medium containing 0.0001-10.0 µg/ml of h-rEGF for 15 minutes, and incubated with 8% ethanol for 1 hour. In another study the above experiment was repeated but cells were pretreated with 10⁻⁴ or 10⁻⁵ M indomethacin before EGF treatment. The cell viability was assessed by fast green exclusion test. Incubation of SEC with 8% ethanol significantly reduced SEC cell viability to 50 ₋⁺ 2%: EGF 0.1 or 1.0/µg/ml significantly reduced ethanol induced damage (cell viability 59 ₋⁺ 3 and 62₋⁺ 3% respectively). Pretreatment with 10⁻⁴ M indomethacin (the dose which does not affect SEC viability but inhibit PGE₂ and PGI₂ generation), significantly reduced protective action of EGF against 8% ethanol injury. EGF 1.0 and 10.0 µg/ml alone without ethanol increased PGE₂ and 6 keto PGF₁α generation by SEC. These studies demonstrated: 1) EGF is able to protect gastric surface epithelial cells directly without mediation by systemic factors. 2) EGF induced protection of SEC may in part be mediated by prostaglandins.

Wydawca

-

Rocznik

Tom

43

Numer

4

Opis fizyczny

p.323-332,fig.

Twórcy

autor
  • DVA Medical Center 5901 E. Seventh Street Long Beach, CA 90822, USA
autor
autor
autor

Bibliografia

  • 1. 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.
  • 2. Olsen PS. Role of epidermal growth factor in gastroduodenal mucosa protection. J Clin Gastroenterol 1988; (Suppl 1): S146-151.
  • 3. Olsen PS, Poulsen SS, Kirkegaard P, Nexo E. Effect of sialoadenectomy and synthetic human urogastrone on healing of chronic gastric ulcers in rats. Gut 1988; 27: 1443-1449.
  • 4. Konturek SJ, Dembinski A, Warzecha T, et al. Role of epidermal growth factor in healing of chronic gastroduodenal ulcer in rats. Gastroenterology 1986; 94: 1300-1307.
  • 5. Itoh M, Joh T, Imai S, et al. Experimental and clinical studies on epidermal growth factor for gastric mucosal protection and healing of gastric ulcers. J Clin Gastroenterol 1988; 10 (Suppl 1): S7-12.
  • 6. Amagase H, Murakami T, Misaki M, et al. Possible mechanism of gastric mucosal protection by epidermal growth factor in rats. Life Sci 1990; 47: 1203-1211.
  • 7. Konturek PK, Brzozowski T, Konturek SJ, et al. Role of epidermal growth factor, prostaglandin, and sulfhydryls in stress-induced gastric lesions. Gastroenterology, 1990; 99: 1607-1615.
  • 8. Matuoka K, Tanaka M, Mitsui Y, Murota S-J. Cultured rabbit gastric epithelial cells producing prostaglandin I2. Gastroenterology 1983; 84: 498-505.
  • 9. Arakawa T, Tarnawski A, Mach T, et al. Impaired generation of prostaglandins from isolated gastric surface epithelial cells in portal hypertensive rats. Prostaglandins 1990; 40 (4): 373-382.
  • 10. Weisenthal LM, Marsden JA, Dill PL, et al. A novel dye exclusion method for testing in vitro chemosensitivity of human tumors. Cancer Res 1983; 43: 749-757.
  • 11. Tarnawski A, Brzozowski T, Sarfeh I J, et al. Prostaglandin production of human isolated gastric glands against irrdomethacin and ethanol injury. J Clin Invest 1988; 81: 1081-1089.
  • 12. Glantz SA. Primer of biostaistics. 2nd ed. New York: McGraw-Hill 1987: 332.
  • 13. Konturek SJ, Brzozowski T, Bielański W, et al. Epidermal growth factor in the gastroprotective and ulcer-healing action of sucralfate in rats. Am J Med 1989; 86 (Suppl 6A): 32-37.
  • 14. Ishikawa T, Sugiyama M, Tsuchiya S. The effect of epidermal growth factor against ethanol induced injury. Cytoprotection & Biology (in press).
  • 15. Olsen PS, Poulsen SS, Kirkegaard P, Nexo E. Role of submandibular saliva and epidermal growth factor in gastric cytoprotection. Gastroenterology 1984; 87: 103-108.
  • 16. Arakawa T, Nakamura A, Fukuda T, et al. Protection of isolated rat gastric cells by prostaglandins from damage caused by ethanol. J Clin Gastroenterol 1988; 10 (Suppl 1): S28-33.
  • 17. Konda Y, Nishizaki H, Nakano O, et al. Prostaglandin protects isolated guinea pig chief cells against ethanol injury via an increase in diacylglycerol. J Clin Invest 1990; 86: 1897-1903.
  • 18. Hiraishi H, Terano A, Ota S, Ishii M, Ivey KJ, Sugimoto T. Epidermal growth factor protects rat gastric mucosal cells against indomethacin-induced damage in monolayer culture. Gastroenterology 1984; 86: 1113.
  • 19. Chiba T, Hirata Y, Tanimoto T. Epidermal growth factor stimulates prostaglandin E release from isolated perfused rat stomach. Biochem Biophys Res Comm 1982; 105: 370-374.
  • 20. Hatt JH, Hanson PJ. Inhibition of gastric acid secretion by epidermal growth factor. Effects on cyclic AMP and on prostaglandin production in rat isolated parietal cells. Biochem J 1988; 255: 789-794.
  • 21. Kuroda H. Effects of phorbol esters and various growth factors on prostaglandin E₂ synthesis by cultured porcine thyroid cells. Nippon Naibunpi Gakkai Zassi - Folia Endocrinologica Japonica 1988; 64: (2): 138-153.
  • 22. Kasai K, Hiraiwa M, Emoto T, et al. Stimulation of prostaglandin E₂ production by phorbol esters and epidermal growth factor in porcine thyroid cells. Life Sci 1987; 41 (2): 241-7.
  • 23. Magnolis BL, Bonventre JV, Kremer SG, et al. Epidermal growth factor is synergistic with phorbol esters and vasopressin in stimulating arachidonate release and prostaglandin production in renal glomerular mesangial cells. Biochem J 1988; 249: 587-592.
  • 24. Blay J, Hollenberg MD. Epidermal growth factor stimulation of prostacyclin production by cultured aortic smooth muscle cells: Requirement for increased cellular calcium levels. J Cell Physiol 1989; 139 (3): 524-302.

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Bibliografia

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