Experimental Studies of Intestinal Ion and Water Transport

References

• Ussing H H, Zerahn K. Active transport of sodium as the source of electric current in the short-circuited isolated frog skin. Acta Physiol Scand 1951; 23: 110–27
   PubMedGoogle Scholar
• Ussing H H. The distinction by means of tracers between active transport and diffusion. Acta Physiol Scand 1949; 19: 43–56
   Google Scholar
• Ussing H H. Does active transport exist?. J Membr Biol 1994; 137: 91–8
   PubMedGoogle Scholar
• Hviid Larsen E. NaCl transport in amphibian skin. Advances in comparative and environmental physiology, R. Greger. Springer-Verlag, Berlin 1988; 189–248
   Google Scholar
• Krogh A. Osmotic regulation in aquatic animals. Cambridge University Press, Cambridge 1939
   Google Scholar
• Zerahn K. Oxygen consumption and active transport in the isolated and short-circuited frog skin. Acta Physiol Scand 1956; 36: 300–18
   PubMedGoogle Scholar
• Holtug K, Skadhauge E. Ion transport across isolated pig jejunum. Am J Physiol 1991; 260: G220–31
   PubMed Web of Science ®Google Scholar
• Choshniak I, Munck B G, Skadhauge E. Sodium chloride transport across the chicken coprodeum. Basic characteristics and dependence on sodium chloride intake. J Physiol Lond 1977; 271: 489–504
   Google Scholar
• Koefoed-Johnsen V, Ussing H H. The nature of the frog skin potential. Acta Physiol Scand 1958; 42: 298–308
   PubMedGoogle Scholar
• Skou J C. The influence of some cations on adenosinetriphosphatase from peripheral nerves. Biochim Biophys Acta 1957; 23: 394–401
   PubMed Web of Science ®Google Scholar
• Skadhauge E. Renal and cloacal salt and water transport in the fowl (Gallus domesticus). Danish Med Bull 1973; 20(Suppl I)1–82
   PubMedGoogle Scholar
• Lange S, Lönnroth I, Skadhauge E. Effects of the antisecretory factor in pigs. Pflugers Arch 1987; 409: 328–32
   PubMed Web of Science ®Google Scholar
• McEwan G T, Schousboe B, Nielsen C G, Skadhauge E. Effect of age on the secretory capacity of pig small intestine in vivo and in vitro. Am J Physiol 1990; 259: G474–80
   PubMed Web of Science ®Google Scholar
• Ussing H H, Bindslev N, Lassen N A, Sten-Knudsen O. Water transport across epithelia. Alfred Benzon Symposium 15. Munksgaard, Copenhagen 1981
   Google Scholar
• Ussing H H, Nedergaard S. Recycling of electrolytes in small intestine of toad. Isotonic transport in leaky epithelia. Alfred Benzon Symposium 34, H H Ussing, J Fischbarg, O Sten-Knudsen, N A Lassen, N J Willumsen. Munksgaard, Copenhagen 1993; 25–34
   Google Scholar
• Rostgaard J. Om salt-og vandtransporterende epitel. En lysog elektronmikroskopisk undersøgelse med funktionelle aspekter. Munksgaard, Copenhagen 1982
   Google Scholar
• Zeuthen T. From contractile vacuole to leaky epithelia. Coupling between salt and water fluxes in biological membranes. Biochim Biophys Acta 1992; 1113: 229–58
   PubMedGoogle Scholar
• Zeuthen T, Stein W D. Cotransport of salt and water in membrane proteins: membrane proteins as osmotic engines. J Membr Biol 1994; 137: 179–95
   PubMedGoogle Scholar
• Nielsen S, Smith B L, Christensen El Agre P. Distribution of the aquaporin CHIP in secretory and resorptive epithelia and capillary endothelia. Proc Natl Acad Sci USA 1993; 90: 7275–9
   PubMed Web of Science ®Google Scholar
• Skadhauge E. Osmoregulation in birds. Springer-Verlag, Berlin, Heidelberg, New York 1981
   Google Scholar
• Bindslev N, Skadhauge E. Sodium chloride absorption and solute-linked water flow across the epithelium of the coprodeum and large intestine in the normal and dehydrated fowl (Gallus domesticus). In vivo perfusion studies. J Physiol Lond 1971; 216: 753–68
   Google Scholar
• Bindslev N, Skadhauge E. Salt and water permeability of the epithelium of the coprodeum and large intestine in the normal and dehydrated fowl (Gallus domesticus). In vivo perfusion studies. J Physiol Lond 1971; 216: 735–51
   Google Scholar
• Hansen M B, Skadhauge E. New aspects of pathophysiology and treatment of secretory diarrhoea. Physiol Res 1995; 44: 61–78
   PubMedGoogle Scholar
• Slender S, Kristensen K, Skadhauge E. Solvent drag by solute-linked water flow. J Membr Biol 1973; 11: 377–98
   PubMedGoogle Scholar
• Holtug K, Shipley A, Dantzer V, Sten Knudsen O, Skadhauge E. Localization of sodium absorption and chloride secretion in an intestinal epithelium. J Membr Biol 1991; 122: 215–29
   PubMedGoogle Scholar
• Andersen V, Hansen G H, Sjostrom H, Noren O. The occurrence of aminopeptidase N and desquamated cell proteins in intestinal perfusate of the rat. Biochim Biophys Acta 1988; 967: 43–8
   PubMedGoogle Scholar
• Sangild P T, Diernæs L, Christiansen I J, Skadhauge E. Intestinal transport of sodium, glucose and immunoglobulin in neonatal pigs. Effect of glucocorticoids. Exp Physiol 1993; 78: 485–97
   PubMed Web of Science ®Google Scholar
• Munck B G. Intestinal absorption of amino acids. Physiology of the gastrointestinal tract, L R Johnson. Raven Press, New York 1981; 1097–122
   Google Scholar
• Munck B G. Transport of neutral and cationic amino acids across the brush-border membrane of rabbit ileum. J Membr Biol 1985; 83: 1–13
   PubMedGoogle Scholar
• Munck B G. Transport of imino and non-alpha-amino acids across the brush border membrane of rabbit ileum. J Membr Biol 1985; 83: 15–24
   PubMedGoogle Scholar
• Munck L K. Chloride-dependent amino acid transport in the small intestine: occurrence and significance. Biochim Biophys Acta 1995, In press.
   Google Scholar
• Munck L K. Cotransport of 2-methyl-aminoisobutyric acid and chloride in rabbit small intestine. Am J Physiol 1993; 265: G979–86
   Google Scholar
• Munck L K, Munck B G. Distinction between chloride-dependent transport systems for taurine and β-alanine in rabbit ileum. Am J Physiol 1992; 262: G609–15
   Google Scholar
• Munck L K. Chloride dependent amino acid transport in the human small intestine. Gut 1995; 36: 215–19
   PubMedGoogle Scholar
• Fahrenkrug J, Haglund U, Jodal M, Lukacs G L, Olbe L, Schaffalitzky de Muckadell O B. Nervous release of vasoactive intestinal polypeptide in the gastrointestinal tract of cats: possible physiological implications. J Physiol Lond 1978; 284: 291–305
   Google Scholar
• Munck L K, Mertz-Nielsen A, Westh H, Bukhave K, Beubler E, Rask-Madsen J. Prostaglandin E2 is a mediator of 5-hydroxytryptamine induced water and electrolyte secretion in the human jejunum. Gut 1988; 29: 1337–41
   PubMed Web of Science ®Google Scholar
• Hansen M B, Thorbøll J E, Christensen P, Bindslev N, Skadhauge E. Serotonin-induced short-circuit current in pig jejunum. J Vet Med 1994; A41: 110–20
   Google Scholar
• Gustafsen J, Lendorf A, Raskov H, Boesby S. Ketanserin versus placebo in carcinoid syndrome. A clinical controlled trial. Scand J Gastroenterol 1986; 21: 816–8
   PubMed Web of Science ®Google Scholar
• Rask-Madsen J, Bukhave K, Beubler E. Influence on intestinal secretion of eicosanoids. J Intern Med Suppl 1990; 732: 137–4.
   PubMedGoogle Scholar
• Hansen M B, Thorbøll J E, Beubler E, Skadhauge E. Effect of indomethacin, renzapride, methysergide, ketanserin, granisetron and citalopram on 5HT-induced fluid accumulation in pig jejunum. Physiol Res 1994; 43: 83–93
   PubMedGoogle Scholar
• McEwan G T, Schousboe B, Skadhauge E. Effect of anti-secretory factor onEscherichia coli STa enterotoxin-induced alkalinisation of pig. Pflugers Arch 1990; 417: 174–9
   PubMedGoogle Scholar
• Hoist J J. Hormonal regulation of digestive secretions. Molecular and cellular basis of digestion, P Desnuelle, H Sjøstrøm, O. Noren. Elsevier, Copenhagen 1986; 77–110
   Google Scholar
• Munck L K, Eskerod O, Hansen M B, Bukhave K, Rask-Madsen J. Failure of tropisetron to inhibit jejunal water and electrolyte secretion induced by 5-hydroxytryptamine in healthy volunteers. Gut 1994; 35: 637–40
   PubMed Web of Science ®Google Scholar
• Rask-Madsen J, Hjelt K. Effect of amiloride on electrical activity and electrolyte transport in human colon. Scand J Gastroenterol 1977; 12: 1–6
   PubMed Web of Science ®Google Scholar
• Arnason S S, Rice G E, Chadwick A, Skadhauge E. Plasma levels of arginine vasotocin, prolactin, aldosterone and corticosterone during prolonged dehydration in the domestic fowl: effect of dietary NaCl. J Comp Physiol B 1986; 156: 383–97
   PubMedGoogle Scholar
• Clauss W, Arnason S S, Munck B G, Skadhauge E. Aldosterone-induced sodium transport in lower intestine. Effects of varying NaCl intake. Pflugers Arch 1984; 401: 354–60
   PubMedGoogle Scholar
• Clauss W, Dantzer V, Skadhauge E. A low-salt diet facilitates Cl secretion in hen lower intestine. J Membr Biol 1988; 102: 83–96
   PubMed Web of Science ®Google Scholar
• Mayhew T M, Elbrond V S, Dantzer V, Skadhauge E, Møller O. Structural and enzymatic studies on the plasma membrane domains and sodium pump enzymes of absorptive epithelial cells in the avian lower intestine. Cell Tissue Res 1992; 270: 577–85
   PubMedGoogle Scholar
• Christensen O, Bindslev N. Fluctuation analysis of short-circuit current in a warm-blooded sodium-retaining epithelium: site current, density, and interaction with triamterene. J Membr Biol 1982; 65: 19–30
   PubMedGoogle Scholar
• Elbrønd V S, Dantzer V, Mayhew T M, Skadhauge E. Avian lower intestine adapts to dietary salt (NaCl) depletion by increasing transepithelial sodium transport and microvillous membrane surface area. Exp Physiol 1991; 76: 733–44
   PubMedGoogle Scholar
• Clauss W, Durr J E, Guth D, Skadhauge E. Effects of adrenal steroids on Na transport in the lower intestine (coprodeum) of the hen. J Membr Biol 1987; 96: 141–52
   PubMedGoogle Scholar
• Holtug K, Hove H, Mortensen P B. Stimulation of butyrate absorption in the human rectum in vivo. Scand J Gastroenterol 1995, In press.
   PubMedGoogle Scholar
• Holtug K, Clausen M R, Hove H, Christiansen J, Mortensen P B. The colon in carbohydrate malabsorption: short chain fatty acids, pH, and osmotic diarrhoea. Scand J Gastroenterol 1992; 27: 545–52
   PubMed Web of Science ®Google Scholar
• Beubler E, Kollar G, Saria A, Bukhave K, Rask-Madsen J. Involvement of 5-hydroxytryptamine, prostaglandin E2, and cyclic adenosine monophosphate in cholera toxin-induced fluid secretion in the small intestine of the rat in vivo. Gastroenterology 1989; 96: 368–76
   PubMed Web of Science ®Google Scholar
• Hansen M B, Thorbøll J, Skadhauge E. 5-HT2 and 5-HT3 receptors mediate serotonin-induced short-circuit current in pig jejunum. J Comp Physiol B 1994; 164: 343–48
   PubMedGoogle Scholar
• Hansen M B, Bindslev N. Serotonin-induced chloride secretion in hen colon. Possible second messengers. Comp Biochem Physiol 1989; 94A: 315–21
   Google Scholar