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. 1975 Nov;252(2):379–396. doi: 10.1113/jphysiol.1975.sp011149

Secretion of electrolytes by the pancreas of the anaestetized rat.

W A Sewell, J A Young
PMCID: PMC1348450  PMID: 1206529

Abstract

1. HCO-3, Na+ and K+ concentrations were measured in bile-free pancreatic juice collected from fasted and fed anaesthetized rats. 2. Resting flow rates averaged 0.62 mul. g-1 .min-1 (fasted) and 2.8 mul. g-1. min-1 (fed) and the mean HCO-3 concentrations, respectively, were 25.8 and 33.3 mM. 3. In fasted rats, instillation of HCl into the duodenum caused flow rate to increase threefold and HCO-3 concentrations to double (66 mM). Intravenous infusion of pure natural (GIH) secretin caused a fivefold increase in flow rate; HCO-3 concentrations, again, doubled (67.5 mM). Infusion of synthetic secretin produced effects essentially the same as those produced by GIH secretin. 4. Infusion of Boots secretin caused a thirteenfold increase in flow rate (8.32 mul.g-1. min-1) but HCO-3 concentrations rose only slightly (43.3 mM). However, following cessation of infusion, when flow rate approximated the maximum obtained with pure secretin, the HCO-3 concentration was much higher (57.2 mM at 3.19 uml.g-1.min-1). In fed animals the responses were similar but maximum flow rates were greater (12 mul. g-1. min-1). 5. Infusion of caerulein produced a secretory rate slightly less than with Boots secretin (5.06 mul. g-1.min-1) and HCO-3 concentrations were plasmalike (30.2 mM); infusion of the synthetic octapeptide of cholecystokinin (OP-CCK) gave similar flow rates and HCO-3 concentrations. 6. Infusion of a mixture of caerulein and GIH secretin mimicked closely the effect of Boots secretin. At maximum flow rates (7.6 mul. g-1. min-1) the HCO-3 concentration was 43.7 mM and at lower flow rates (3.90 mul.g-1. min-1) it rose to 54.2mM. 7. It is concluded that the response of the rat pancreas to secretin is qualitatively similar to that of all other vertebrates so far studied, but, relative to other animals, the response is sluggish. In contrast, the rat pancreas responds well to cholecystokinin (CCK) stimulation, yielding a juice with plasma-like HCO-3 concentration. Boots secretin, which is heavily contaminated with CCK, causes a mixed response resembling that of CCK at high secretory rates and that of pure secretin at lower rates. 8. An unexplained feature of rat pancreatic juice was that K+ concentrations, although plasma-like in unstimulated samples, rose to about 8mM when flow rate increases as a result of secretin, but not CCK, stimulation. In all other animals so far studied, the K+ concentration has been found to be independent of flow rate.

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Selected References

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  1. BRO-RASMUSSEN F., KILLMANN S. A., THAYSEN J. H. The composition of pancreatic juice as compared to sweat, parotid saliva and tears. Acta Physiol Scand. 1956 Sep 26;37(2-3):97–113. doi: 10.1111/j.1748-1716.1956.tb01346.x. [DOI] [PubMed] [Google Scholar]
  2. BURGEN A. S. The secretion of potassium in saliva. J Physiol. 1956 Apr 27;132(1):20–39. doi: 10.1113/jphysiol.1956.sp005500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bayliss W. M., Starling E. H. On the uniformity of the pancreatic mechanism in vertebrata. J Physiol. 1903 Mar 16;29(2):174–180. doi: 10.1113/jphysiol.1903.sp000948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bayliss W. M., Starling E. H. The mechanism of pancreatic secretion. J Physiol. 1902 Sep 12;28(5):325–353. doi: 10.1113/jphysiol.1902.sp000920. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bertaccini G., De Caro G., Endean R., Erspamer V., Impicciatore M. The action of caerulein on pancreatic secretion of the dog and biliary secretion of the dog and the rat. Br J Pharmacol. 1969 Sep;37(1):185–197. doi: 10.1111/j.1476-5381.1969.tb09537.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Brown J. C., Harper A. A., Scratcherd T. Potentiation of secretin stimulation of the pancreas. J Physiol. 1967 Jun;190(3):519–530. doi: 10.1113/jphysiol.1967.sp008225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. CRICK J., HARPER A. A., RAPER H. S. On the preparation of secretin and pancreozymin. J Physiol. 1949 Dec;110(3-4):367–376. doi: 10.1113/jphysiol.1949.sp004445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Case R. M., Harper A. A., Scratcherd T. The secretion of electrolytes and enzymes by the pancreas of the anaesthetized cat. J Physiol. 1969 Apr;201(2):335–348. doi: 10.1113/jphysiol.1969.sp008759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DEBRAY C., DE LA TOUR J., VAILLE C., ROZE C., SOUCHARD M. [Contribution to the study of the biliary and external pancreatic secretion in the rat]. J Physiol (Paris) 1962 May-Jun;54:459–499. [PubMed] [Google Scholar]
  10. DORCHESTER J. E. C., HAIST R. E. The secretin content of the intestine in normal and hypophysectomized rats. J Physiol. 1952 Oct;118(2):188–195. doi: 10.1113/jphysiol.1952.sp004785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. DREILING D. A., JANOWITZ H. D. The secretion of electrolytes by the human pancreas; the effect of diamox, ACTH, and disease. Am J Dig Dis. 1959 Feb;4(2):127–144. doi: 10.1007/BF02231234. [DOI] [PubMed] [Google Scholar]
  12. Debas H. T., Grossman M. I. Pure cholecystokinin: pancreatic protein and bicarbonate response. Digestion. 1973;9(6):469–481. doi: 10.1159/000197476. [DOI] [PubMed] [Google Scholar]
  13. Debray C., Vaille C., De la Tour J., Rozé C., Souchard M., Chariot J., Fox A. Action de la céruléine sur la sécrétion pancréatique externe du rat: cinétique et relation dose-effet. Biol Gastroenterol (Paris) 1973 Mar;6(2):97–104. [PubMed] [Google Scholar]
  14. Dockray G. J. The action of scretin, cholecystokinin-pancreozymin and caerulein on pancreatic secretion in the rat. J Physiol. 1972 Sep;225(3):679–692. doi: 10.1113/jphysiol.1972.sp009963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Erspamer V. Progress report: caerulein. Gut. 1970 Jan;11(1):79–87. doi: 10.1136/gut.11.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ertan A., Brooks F. P., Ostrow J. D., Arvan D. A., Williams C. N., Cerda J. J. Effect of jejunal amino acid perfusion and exogenous cholecystokinin on the exocrine pancreatic and biliary secretions in man. Gastroenterology. 1971 Nov;61(5):686–692. [PubMed] [Google Scholar]
  17. GROSSMAN M. I. Pancreatic secretion in the rat. Am J Physiol. 1958 Sep;194(3):535–539. doi: 10.1152/ajplegacy.1958.194.3.535. [DOI] [PubMed] [Google Scholar]
  18. Greenwell J. R. The effects of cholecystokinin-pancreozymin, acetylcholine and secretin on the membrane potentials of mouse pancreatic cells in vitro. Pflugers Arch. 1975;353(2):159–170. doi: 10.1007/BF00599876. [DOI] [PubMed] [Google Scholar]
  19. HERRIOTT B. A., SINNETT P. F., PALMER A. A. THE OCCURRENCE IN THE RAT OF AN ACCESSORY PANCREATIC DUCT OPENING DIRECTLY INTO THE DUODENUM. Aust J Exp Biol Med Sci. 1965 Apr;43:175–184. doi: 10.1038/icb.1965.16. [DOI] [PubMed] [Google Scholar]
  20. HIRSCH G. C., JUNQUEIRA L. C., ROTHSCHILD H. A., DOHI S. R. Die Pankreassaft-Sekretion bei der Ratte. I. Die kontinuierliche, irreguläre Hungersekretion und ihre Ursachen. Pflugers Arch. 1957;264(1):78–87. doi: 10.1007/BF00412574. [DOI] [PubMed] [Google Scholar]
  21. Harper A. A. The control of pancreatic secretion. Gut. 1972 Apr;13(4):308–317. doi: 10.1136/gut.13.4.308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Heatley N. G. The assay of pancreozymin, and of secretin and pancreozymin simultaneously, in the rat. J Endocrinol. 1968 Dec;42(4):549–557. doi: 10.1677/joe.0.0420549. [DOI] [PubMed] [Google Scholar]
  23. Heatley N. G. The assay of secretin in the rat. J Endocrinol. 1968 Dec;42(4):535–547. doi: 10.1677/joe.0.0420535. [DOI] [PubMed] [Google Scholar]
  24. Hickson J. C. The secretion of pancreatic juice in response to stimulation of the vagus nerves in the pig. J Physiol. 1970 Feb;206(2):275–297. doi: 10.1113/jphysiol.1970.sp009013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. LAGERLOF H., EK S. Y., NYBERG A. The duodenal secretion in man as a function of secretin dose and secretin inactivation. Gastroenterology. 1962 Aug;43:174–180. [PubMed] [Google Scholar]
  26. LIN T. M., ALPHIN R. S. Comparative bio-assay of secretin and pancreozymin in rats and dogs. Am J Physiol. 1962 Nov;203:926–928. doi: 10.1152/ajplegacy.1962.203.5.926. [DOI] [PubMed] [Google Scholar]
  27. LIN T. M., ALPHIN R. S. Vagal secretory nerves for pancreatic secretion in the rat. Am J Physiol. 1959 Sep;197:555–557. doi: 10.1152/ajplegacy.1959.197.3.555. [DOI] [PubMed] [Google Scholar]
  28. LOVE J. W. A method for the assay of secretin, using rats. Q J Exp Physiol Cogn Med Sci. 1957 Jul;42(3):279–284. doi: 10.1113/expphysiol.1957.sp001263. [DOI] [PubMed] [Google Scholar]
  29. Lehnert P., Stahlheber H., Forell M. M., Fritz H., Werle E. Kinetics of exocrine pancreatic secretion. Digestion. 1972;6(1):9–22. doi: 10.1159/000197218. [DOI] [PubMed] [Google Scholar]
  30. Mangos J. A., McSherry N. R. Micropuncture study of excretion of water and electrolytes by the pancreas. Am J Physiol. 1971 Aug;221(2):496–503. doi: 10.1152/ajplegacy.1971.221.2.496. [DOI] [PubMed] [Google Scholar]
  31. Mangos J. A., McSherry N. R., Nousia-Arvanitakis S., Schilling R. F. Transductal fluxes of anions in the rat pancreas. Proc Soc Exp Biol Med. 1974 May;146(1):321–328. doi: 10.3181/00379727-146-38097. [DOI] [PubMed] [Google Scholar]
  32. NATELSON S. Routine use of ultramicro methods in the clinical laboratory; estimation of sodium, potassium, chloride, protein, hematocrit value, sugar, urea and nonprotein nitrogen in fingertip blood; construction of ultramicro pipets; a practical microgasometer for estimation of carbon dioxide. Am J Clin Pathol. 1951 Dec;21(12):1153–1172. [PubMed] [Google Scholar]
  33. Petersen O. H., Ueda N. Pancreatic acinar cells: effect of acetylcholine, pancreozymin, gastrin and secretin on membrane potential and resistance in vivo and in vitro. J Physiol. 1975 May;247(2):461–471. doi: 10.1113/jphysiol.1975.sp010941. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. ROTHMAN S. S. EXOCRINE SECRETION FROM THE ISOLATED RABBIT PANCREAS. Nature. 1964 Oct 3;204:84–85. doi: 10.1038/204084a0. [DOI] [PubMed] [Google Scholar]
  35. Ramirez J., Hubel K. A., Clifton J. A. Intestinal factors affecting pancreatic exocrine secretion in the rat. Am J Physiol. 1966 Jul;211(1):260–263. doi: 10.1152/ajplegacy.1966.211.1.260. [DOI] [PubMed] [Google Scholar]
  36. Shaw H. M., Heath T. The significance of hormones, bile salts, and feeding in the regulation of bile and other digestive secretions in the rat. Aust J Biol Sci. 1972 Feb;25(1):147–154. [PubMed] [Google Scholar]
  37. Stening G. F., Grossman M. I. Gastrin-related peptides as stimulants of pancreatic and gastric secretion. Am J Physiol. 1969 Jul;217(1):262–266. doi: 10.1152/ajplegacy.1969.217.1.262. [DOI] [PubMed] [Google Scholar]
  38. Ternouth J. H., Buttle H. L. Concurrent studies on the flow of digesta in the duodenum and of exocrine pancreatic secretion of calves. The collection of the exocrine pancreatic secretion from a duodenal cannula. Br J Nutr. 1973 May;29(3):387–397. doi: 10.1079/bjn19730116. [DOI] [PubMed] [Google Scholar]

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