Skip to main content
Log in

Intraepithelial current flow in rat pancreatic secretory epithelia

  • Transport in Intact Epithelia and Its Regulation
  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

To assess the importance for transepithelial salt secretion of current flow across the baso-lateral membrane, we studied the effects of ouabain (1 mmol/l), Ba (3 mmol/l) and tetraethylammonium (TEA: 10 mmol/l) on secretion by the acinar (caerulein stimulated) and ductal (secretin stimulated) epithelia of the perfused rat pancreas. Within 10 min, ouabain caused a 79% inhibition of acinar secretion which was resolvable into two exponentials with half-times, respectively, of 0.24 min±0.19 (S.D.) and 6.40±0.46 min. In contrast, it caused only a monoexponential inhibition of ductal secretion (61% in 10 min) with a half-time of 5.08±0.26 min. Ba caused a monoexponential inhibition of acinar secretion (70% in 10 min) with a half-time of 1.82±0.27 min, but it had no inhibitory effect on ductal secretion. The action of TEA was similar to that of Ba: it caused monoexponential inhibition of acinar secretion (26% in 10 min) with a half-time of 1.82±0.03 min, and it too had no effect on ductal secretion. For comparison, we also studied the effect of these drugs on the more rapidly secreting rat mandibular gland (stimulated with acetylcholine). All three drugs were strongly inhibitory: within 10 min, ouabain caused a 95%, Ba an 89% and TEA an 83% inhibition. The decay curves appeared to be monoexponential with halftimes, respectively, of 1.49±0.12, 0.51±0.3 and 0.56±0.02 min. The results support the hypothesis that current flow across the baso-lateral membrane is an important concomitant of secretion by the pancreatic acinar epithelium and by mandibular glands, but they suggest that such a current is not important for secretion by pancreatic ducts.

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. Allen DG, Eisner DA, Wray SC (1985) Sodium pump: birthday present. Nature 316:674–675

    Google Scholar 

  2. Bundgaard M, Møller M, Poulsen JH (1977) Localization of sodium pump sites in cat salivary glands. J Physiol (Lond) 273:339–353

    Google Scholar 

  3. Case RM, Conigrave AD, Novak I, Young JA (1980) Electrolyte and protein secretion by the perfused rabbit mandibular gland stimulated with acetylcholine or catecholamines. J Physiol (Lond) 300:467–487

    Google Scholar 

  4. Case RM, Hunter M, Novak I, Young JA (1984) The anionic basis of fluid secretion by the rabbit mandibular gland. J Physiol (Lond) 349:619–630

    Google Scholar 

  5. Findlay I, Petersen OH (1985) Acetylcholine stimulates a Ca2+-dependent Cl conductance in mouse lacrimal acinar cells. Pflügers Arch 403:328–330

    Google Scholar 

  6. Fölsch UR, Creutzfeldt W (1977) Pancreatic duct cells in rats: secretory studies in response to secretin, cholecystokininpancreozymin, and gastrin in vivo. Gastroenterology 73:1053–1059

    Google Scholar 

  7. Greger R, Schlatter E (1984) Mechanism of NaCl secretion in rectal gland tubules of spiny dogfish (Squalus acanthias). II. Effect of inhibitors. Pflügers Arch 402:364–375

    Google Scholar 

  8. Greger R, Schlatter E, Gögelein H (1985) Cl-channels in the apical cell membrane of the rectal gland “induced” by cAMP. Pflügers Arch 406:446–448

    Google Scholar 

  9. Hansen TR, Dineen DX, Petrak R (1984) Mechanism of action of barium ion on rat aortic smooth muscle. Am J Physiol 246:C235-C241

    Google Scholar 

  10. Higgins JT, Gebler B, Frömter E (1977) Electrical properties of amphibian urinary bladder epithelia. II. The cell potential profile inNecturus maculosus. Pflügers Arch 371:87–97

    Google Scholar 

  11. Iwatsuki N, Petersen OH (1985) Action of tetraethylammonium on calcium-activated potassium channels in pig pancreatic acinar cells studied by patch-clamp single-channel and whole-cell current recording. J Membr Biol 86:139–144

    Google Scholar 

  12. Iwatsuki N, Petersen OH (1985) Inhibition of Ca2+-activated K+ channels in pig pancreatic acinar cells by Ba2+, Ca2+, quinine and quinidine. Biochim Biophys Acta 819:249–257

    Google Scholar 

  13. Kempen HJM, De Pont JJHHM, Bonting SL (1977) Rat pancreas adenylate cyclase. V. Its preference in isolated rat pancreatic acinar cells. Biochim Biophys Acta 496:521–531

    Google Scholar 

  14. Klyce SD, Wong RK (1977) Site and mode of adrenaline action on chloride transport across the rabbit corneal epithelium. J Physiol (Lond) 266:777–799

    Google Scholar 

  15. Lingard JM, Young JA (1983) β-Adrenergic control of exocrine secretion by perfused rat pancreas in vitro. Am J Physiol 245:G690-G696

    Google Scholar 

  16. Machen TE, Forte JG (1984) Anion secretion by gastric mucosa. In: Gerencser GA (ed) Chloride transport coupling in biological membranes and epithelia. Elsevier, Amsterdam, pp 415–446

    Google Scholar 

  17. Martinez JR, Cassity N (1985)36Cl fluxes in dispersed rat submandibular acini: effects of acetylcholine and transport inhibitors. Pflügers Arch 403:50–54

    Google Scholar 

  18. Nagel W (1980) Time course of pump inhibition by ouabain in amphibian epithelia. Biochim Biophys Acta 599:736–740

    Google Scholar 

  19. Novak I, Davé C, Young JA (1984) The anionic basis of secretion by rat and rabbit mandibular glands. In: Case RM, Lingard JM, Young JA (eds) Secretion: Mechanisms and Control. Manchester University Press, Manchester, pp 77–80

    Google Scholar 

  20. Petersen OH, Maruyama Y (1984) Calcium-activated potassium channels and their role in secretion. Nature 307:693–696

    Google Scholar 

  21. Poulsen JH, Laugesen LP, Nielsen JOD (1982) Evidence supporting that basolaterally located Na+−K+-ATPase and a co-transport system for sodium and chloride are key elements in secretion of primary saliva. In: Case RM, Garner A, Turnberg LA, Young JA (eds) Electrolyte and water transport across gastrointestinal epithelia. Raven Press, New York, pp 157–159

    Google Scholar 

  22. Saito Y, Ozawa T, Hayashi H, Nishiyama A (1985) Acetylcholine-induced change in intracellular Cl-activity of the mouse lacrimal acinar cells. Pflügers Arch 405:108–126

    Google Scholar 

  23. Schulz I, Ullrich KJ (1979) Transport processes in the exocrine pancreas. In: Giebisch G, Tosteson DC, Ussing HH (eds) Membrane Transport in Biology, Vol IVB, Transport Organs. Springer, Berlin, pp 811–852

    Google Scholar 

  24. Seow FKT, Lingard JM, Young JA (1986) The anionic basis of fluid secretion by rat pancreatic acini in vitro. Am J Physiol 250:G140-G148

    Google Scholar 

  25. Sewell WA, Young JA (1975) Secretion of electrolytes by the pancreas of the anaesthetized rat. J Physiol (Lond) 252:379–396

    Google Scholar 

  26. Silva P, Stoff J, Field M, Fine L, Forrest JN, Epstein FH (1977) Mechanism of active chloride secretion by shark rectal gland: role of Na-K-ATPase in chloride transport. Am J Physiol 233:F298-F306

    Google Scholar 

  27. Welsh MJ (1983) Inhibition of chloride secretion by furosemide in canine tracheal epithelium. J Membr Biol 71:219–226

    Google Scholar 

  28. Welsh MJ (1985) Basolateral membrane potassium conductance is independent of sodium pump activity and membrane voltage in canine tracheal epithelium. J Membr Biol 84:25–33

    Google Scholar 

  29. Welsh MJ, Smith PL, Frizzell RA (1983) Chloride secretion by canine tracheal epithelium. III. Membrane resistances and electromotive forces. J Membr Biol 71:209–218

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Evans, L.A.R., Pirani, D., Cook, D.I. et al. Intraepithelial current flow in rat pancreatic secretory epithelia. Pflugers Arch. 407 (Suppl 2), S107–S111 (1986). https://doi.org/10.1007/BF00584938

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00584938

Key words

Navigation