Skip to main content
Log in

Evidence for rheogenic sodium bicarbonate cotransport in the basolateral membrane of oxyntic cells of frog gastric fundus

  • Transport Processes, Metabolism and Endocrinology; Kidney, Gastrointestinal Tract, and Exocrine Glands
  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

Ionic conductance properties of the basolateral cell membrane of oxyntic cells were studied in frog gastric fundus in vitro. After mounting the fundus in a modified Ussing chamber the serosal connective tissue was dissected off and individual oxyntic cells were punctured from the serosal surface with microelectrodes. Under resting conditions the membrane potential averaged −56.9, SD±9.5 mV (n=63), cytoplasm negative. Lowering or raising serosal HCO 3 concentration from 17.8 to 6 or 36 mmol/l respectively at constant\(p_{CO_2 } \) depolarized or hyperpolarized the cell membrane by +16.7 or −18.2 mV respectively. Sudden removal of serosal Na+ also depolarized the cell membrane (anomalous Nernst response). Since both the HCO 3 dependent and the Na+ dependent potential changes were strongly depressed by the disulfonic stilbene SITS and since the potential response to HCO 3 was virtually abolished in Na+-free solution we conclude that a rheogenic Na+ (HCO 3 ) n -cotransport system (n>1) is present in the basolateral cell membrane of oxyntic cells. Its possible role in base transfer during HCl-secretion or HCO 3 secretion remains to be elucidated.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Bello-Reuss E (1982) Electrical properties of the basolateral membrane of the straight portion of the rabbit proximal renal tubule. J Physiol 326:49–63

    Google Scholar 

  2. Blum AL, Hirschowitz BI, Helander HF, Sachs G (1971) Electrical properties of isolated cells of Necturus gastric mucosa. Biochim Biophys Acta 241:261–272

    Google Scholar 

  3. Boron WF, Boulpaep EL (1983) Intracellular pH regulation in the renal proximal tubule of the salamander. Basolateral HCO 3 -transport. J Gen Physiol 81:53–94

    Google Scholar 

  4. Burckhardt B-Ch, Cassola AC, Frömter E (1984) Electrophysiological analysis of bicarbonate permeation across the peritubular cell membrane of rat kidney proximal tubule. II. Exclusion of HCO 3 -effects on other ion permeabilities and of coupled electroneutral HCO 3 -transport. Pflügers Arch 401: 43–51

    Google Scholar 

  5. Burckhardt B-Ch, Sato K, Frömter E (1984) Electrophysiological analysis of bicarbonate permeation across the peritubular cell membrane of rat kidney proximal tubule. I. Basic observations. Pflügers Arch 401:34–42

    Google Scholar 

  6. Carrasquer G, Chu TC, Rehm WS, Schwartz M (1982) Evidence for electrogenic Na-Cl-symport in the in vitro frog stomach. Am J Physiol 242:G620-G627

    Google Scholar 

  7. Carrasquer G, Kissel D, Rehm WS, Schwartz M (1983) Anomalous potential difference responses to changes in sodium concentration in the antrum of frog stomach. Am J Physiol 245:G554-G561

    Google Scholar 

  8. Curci S, Schettino T (1984) Effect of external sodium on intracellular chloride activity in the surface cells of frog gastric mucosa. Microelectrode studies. Pflügers Arch 401:152–159

    Google Scholar 

  9. Curci S, Schettino T, Frömter E (1986) Histamine reduces Cl activity in surface epithelial cells of frog gastric mucosa. Suggestive evidence for ionic coupling between surface epithelial and oxyntic cells. Pflügers Arch 406:204–211

    Google Scholar 

  10. Demarest JR, Machen TE (1985) Microelectrode measurements from oxyntic cells in intact Necturus gastric mucosa. Am J Physiol 249:C535-C540

    Google Scholar 

  11. Flemström G, Sachs G (1975) Ion transport by amphibian antrum in vitro. I. General characteristics. Am J Physiol 228:1188–1198

    Google Scholar 

  12. Frömter E (1986) The electrophysiological analysis of tubular transport. Kidney Intern 30:216–228

    Google Scholar 

  13. Hogben CAM, Kent TH, Woodward PA, Sill AJ (1974) Qualitative histology of the gastric mucosa: man, dog, cat, guinea pig and frog. Gastroenterology 67:1143–1154

    Google Scholar 

  14. Ito S (1967) Anatomic structure of the gastric mucosa. In: CF Code (ed) Handbook of physiology, alimentary canal, vol 2. Am Physiol Soc, Washington DC, pp705–741

    Google Scholar 

  15. Jentsch TJ, Koller SK, Koch M, Wiederholt M (1984) Evidence for coupled transport of bicarbonate and sodium in cultured bovine corneal endothelial cells. J Membr Biol 81:189–204

    Google Scholar 

  16. Jentsch TJ, Matthes M, Keller SK, Wiederholt M (1985) Anion dependence of electrical effects of bicarbonate and sodium on cultured bovine corneal endothelial cells. Pflügers Arch 403:175–185

    Google Scholar 

  17. Rehm WS, Sanders SS (1975) Implications of the neutral carrier Cl-HCO3-exchange mechanism in the gastric mucosa. Ann N Y Acad Sci 246:442–455

    Google Scholar 

  18. Sanders SS, O'Callaghan J, Butler CF, Rehm WS (1972) Conductance of submucosal-facing membrane of frog gastric mucosa. Am J Physiol 222:1348–1354

    Google Scholar 

  19. Schettino T, Curci S, Ceglie L, Zambonin-Zallone A, Frömter E (1985) Microelectrode studies on oxyntic cells in intact frog gastric mucosa. Congresso SIBS-SIF-SINU, Abstract 51

  20. Schwartz M, Carrasquer G, Rehm WS (1985) Evidence for HCO 3 -conductance pathway in nutrient membrane of bullfrog antrum. Biochim Biophys Acta 816:251–257

    Google Scholar 

  21. Schwartz M, Carrasquer G, Rehm WS (1985) Evidence for HCO 3 -conductance pathways in nutrient membrane of resting frog fundus. Biochim Biophys Acta 819:187–194

    Google Scholar 

  22. Shoemaker RL (1978) Micropuncture studies using the amphibian fundic gastric mucosa, in vitro. In: Öbrink KJ, Flemström G (eds) Gastric ion transport. Acta Physiol Scand (Spec Suppl) pp 173–180

  23. Soleimani M, Grassel SM, Aronson PS (1986) Stoichiometry of the NaHCO 3 cotransport system in renal basolateral membrane vesicles. Clin Res 34:609 A

    Google Scholar 

  24. Villegas L (1962) Cellular location of the electrical potential difference in frog gastric mucosa. Biochim Biophys Acta 64:359–367

    Google Scholar 

  25. Yoshitomi K, Frömter E (1984) Cell pH of rat renal proximal tubule in vivo and the mechanism of peritubular HCO 3 -exit. Pflügers Arch 402:300–305

    Google Scholar 

  26. Yoshitomi K, Burckhardt B-Ch, Frömter E (1985) Rheogenic sodium-bicarbonate cotransport in the peritubular cell membrane of rat renal proximal tubule. Pflügers Arch 405:360–366

    Google Scholar 

  27. Yoshitomi K, Frömter E (1985) How big is the electrochemical potential difference of Na+ across rat renal proximal tubular cell membrane in vivo? Pflügers Arch 405:S121-S126

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported by grants Nr. 85.0443.04 and 86.00048.04 from Consiglio Nazionale delle Ricerche, Rome, Italy and by grant Nr. I 37736 from Stiftung Volkswagenwerk, Hannover, FRG

Rights and permissions

Reprints and permissions

About this article

Cite this article

Curci, S., Debellis, L. & Frömter, E. Evidence for rheogenic sodium bicarbonate cotransport in the basolateral membrane of oxyntic cells of frog gastric fundus. Pflugers Arch. 408, 497–504 (1987). https://doi.org/10.1007/BF00585075

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00585075

Key words

Navigation