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1991 | 42 | 4 |

Tytuł artykułu

Does the membrane potential control incorporation of tubulovesicles into the secreting apical membrane of the rat parietal cell?

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The present studies were designed to examine the effect of changes in membrane potential by means of protonophore carbonyl cyanide m-chlorophenylhydrazone (СССР) and variations in the pH of the medium on the secretory response of parietal cells. Studies were performed in vitro using isolated cells from rat stomachs and acid production was indirectly determined by ¹⁴C-aminopyrine (AP) accumulation. СССР affected both basal and histamine-stimulated AP accumulation in a concentration-dependent manner. The AP accumulation ratios depended on pH of the incubation medium; the ratio was lowest at pH 6.6, and increased progressively as the pH of the medium increased to 7.8. Moreover, the decreases in AP accumulation ratios caused by simultanous addition of СССР and AP to cell suspensions compared to those in which СССР was added to incubated cells after achieving the steady-state of AP accumulation were quantitatively similar. These findings suggest that the decrease in AP accumulation due to СССР treaiment is a consequence of an activation of acid secretion rather than an inhibitor of acid production. From the present and previously published data, we propose a working hypothesis: membrane recycling is dependent on changes in apical membrane potential.

Wydawca

-

Rocznik

Tom

42

Numer

4

Opis fizyczny

p.367-379,fig.,ref.

Twórcy

autor
  • Department of Gastroenterology and Metabolism, Medical Center of Postgraduate Education, Goszczynskiego 1, 02-616 Warsaw, Poland
autor
  • Department of Biophysics and Biomathematics, Medical Center of Postgraduate Education, Goszczynskiego 1, 02-616 Warsaw, Poland
autor
  • Department of Gastroenterology and Metabolism, Medical Center of Postgraduate Education, Goszczynskiego 1, 02-616 Warsaw, Poland
autor
  • Department of Gastroenterology and Metabolism, Medical Center of Postgraduate Education, Goszczynskiego 1, 02-616 Warsaw, Poland

Bibliografia

  • 1. Forte TM, Machen ТЕ, Forte JG. Ultrastructural changes in oxyntic cells associated with secretory function: a membrane recycling hypothesis. Gastroenterology 1977, 73: 941-955.
  • 2. Helander HF, Hirschowitz BI. Quantitative ultrastructural studies on gastric parietal cells. Gastroenterology 1972; 63: 951-961.
  • 3. Zalewsky CA, Moody FG. Stereological analysis of the parietal cell during acid secretion and inhibition. Gastroenterology 1977; 73: 66-74.
  • 4. Dołowy K: Membrane-potential-controlled lipid vesicle recycling and amoeboid locomotion. J. Bioelectricity 1987; 6: 109-128.
  • 5. Gespach Ch, Bataille D, Dupont Ch, Rosselin G, Wunsch E, Jaeger E. Evidence for a cyclic AMP system highly sensitive to secretion in gastric glands isolated from the rat fundus and antrum. Biochim Biophys Acta 1980; 630: 433-441.
  • 6. Ostrowski J, Bomsztyk K. Interaction of signal transduction pathways in mediating acid secre tion by rat parietal cells. Am J Physiol 1989; 256: C873-C879.
  • 7. Felle H, Centrup FW. A study of the primary effect of the uncopupler carbonyl cyanide m-chlorophenylhydrazone on membrane potential and conductance in Riccia flunans Biochim Biophys Acta 1977; 464: 179-187.
  • 8. Le Blanc OH Jr. The effect of uncouplers of oxidative phosphorylation on lipid bilayer membranes: carbonylcyanide-m-chlorophenylhydrazone. J Membrane Biol 1971; 4: 227-751.
  • 9. McLaughlin SGA, Dilger JP. Transport of protons across membranes by weak acids. Physiol Rev 1980; 60, 825-863.
  • 10. Rabon E, Cuppoletti J, Malinowska D, Smolka A, Helander HF, Mendlein J, Sachs G. Proton secretion by the gastric parietal cell J exp Biol 1983; 106: 119-133.
  • 11. Forte JG, Machen TM, Obrink KJ. Mechanisms of gastric H⁺ and Cl⁻ transport. Ann Rev- Physiol 1980; 42: 111-2611.
  • 12. Lorentzon P, Sachs G, Wallmark В. Inhibitory effects of cations on the gastic H⁺, K⁺-ATPase. A potential-sensitive step in the K⁺ limb of the pump cycle. J Biol Chem 1988; 263:10705-10710.
  • 13. Cuppoletti J, Sachs G. Regulation of gastric acid secretion via modulation of a chloride conductance. J Biol Chem 1984; 259: 14952-14959.
  • 14. Paradiso AM, Townsley MC, Wenzl E, Machen ТЕ. Regulation of intracellular pH in resting and stimulated parietal cells. Am J Physiol 1989; 257: C554-C561.
  • 15. Crane EE, Davies RE, Longmuir NM. The effect of electric current on hydrochloric acid secretion by isolated frog gastric mucosa. Biochem J 1948; 43: 321-336.
  • 16. Rehm WS. Effect of electric current on gastric hydrogen ion and chloride secretion. Am J Physiol 1956; 185: 325-331.
  • 17. Rehm WS, Davis TL, Chandler C, Gohmann E Jr, Bashirelahi A. Frog gastric mucosae bathe in chloride-fress solutions. Am J Physiol 1963; 204: 233-242.
  • 18. Rehm WS, Lefevre ME. Effect of dinitrophenol on potential, resistance, and H⁺ rate in frog stomach. Am J Physiol 1965; 208 : 922-930.
  • 19. Rehm WS, Sanders SS. Electrical events during activation and inhibition of gastric HC1 secretion. Gastroenterology 1975; 73: 959-969.
  • 20. Demarest JR, Machen ТЕ. Microelectrode measurements from oxyntic cells in intact Necturus gastric mucosa. Am J Physiol 1985; 23: C535-C540.
  • 21. Ueda S, Loo DDF, Sachs G. Regulation of K⁺ channels in the basolateral membrane of Nectu rus oxyntic cells. J Membrane Biol 1987; 97: 31-41.

Typ dokumentu

Bibliografia

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