Abstract
It has been appreciated for many years that the presence of Na+ in the intestinal lumen enhances and indeed is required for active sugar absorption by the small intestinal mucosa. Since the seminal observation (Riklis and Quastel 1958, Czaky and Thale 1960, Crane et al. 1961) was made there have been numerous studies aimed at characterizing the transport mechanism in the brush border. There is now wide acceptance for the view that Na+ and sugar are bound and cotransported on the same apical membrane carrier (Fig. la). More recently the way in which sugars are translocated across the basolateral membrane have received attention and these studies, pointing to facilitated diffusion of sugar, are serving to round out our view of transcellular sugar transport and sugar absorption. It has also been known for a long time that actively transported sugars stimulate the absorption of Na+ (Fig. lb). For example actively transported sugars increase the transepithelial electrical potential difference (ψms) which is measurable across the wall of the intestine (Barry et al. 1961, Baillien and Schoffeniels 1961, Clarkson et al. 1961, Schachter and Britten 1961). The short-circuit current (Isc) is similarly stimulated as illustrated in Fig. 2 without any early changes in tissues resistance. Phloridzin, which blocks sugar absorption (Newey et al. 1959) blocks the stimulation of Isc.
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References
Armstrong WMcD (1975) Electrophysiology of sodium transport by epithelial cells of the small intestine. In: Czaky TZ (ed) Intestinal absorption and malabsorption. Raven Press, New York, p 45
Armstrong WMcD, Musselman DL, Reitzug HC (1970) Sodium, potassium and water content of isolated bullfrog small intestinal epithelia. Am J Physiol 219:1023–1026
Armstrong WMcD, Bixenman WR, Frey KF, Garcia-Diaz JF, O’Regan MG, Owens JL (1979) Energetics of coupled Na+ and Cl- entry into epithelial cells of bullfrog small intestine. Biochim Biophys Acta 551:207–219
Baillien M, Schoffeniels E (1961) Origin of the potential difference in the intestinal epithelium of the turtle. Nature 190:1107–1108
Barry RJC, Eggenton J (1972) Membrane potentials of epithelial cells in rat small intestine. J Physiol (Lond) 227:201–216
Barry RJC, Dikstein S, Matthews J, Smyth DH (1961) Electrical potentials in the isolated intestine. J Physiol (Lond) 17P-18P
Boulpaep EL (1967) Ion permeability of the peritubular and luminal membrane of the renal tubular cell. In: Krück F (ed) Symposium über Transport und Funktion intracellulärer Elektrolyte. Urban & Schwarzenberg, München, p 98
Brown MM, Parsons DS (1962) Observations on the changes in the potassium content of rat jejunal mucosa during absorption. Biochim Biophys Acta 59:249–251
Cemerikic D, Giebisch G (1980) Intracellular sodium activity in Necturus kidney proximal tubule. Fed Proc 39:1080
Clarkson TW, Cross AC, Toole SR (1961) Dependence on substrate of the electrical potential across the isolated gut. Nature 191:501–502
Crane RK, Miller D, Bihler I (1961) The restrictions on possible mechanisms of intestinal active transport of sugars. In: Kleinzeller A, Kotyk Z (eds) Membrane transport and metabolism. Academic Press, London New York, p 439
Czaky TZ, Esposito G (1969) Osmotic swelling of intestinal epithelial cells during active sugar transport. Am J Physiol 217:753–755
Czaky TZ, Thale M (1960) Effect of ionic environment on intestinal sugar transport. J Physiol (Lond) 151:59–65
Dinno MA, Huang KC (1977) Effect of glucose and diuretics on intracellular potentials of mouse intestinal mucosa. Proc Soc Exp Biol Med 155:71–78
Frömter E (1979) Solute transport across epithelia: What can we learn from micropuncture studies on kidney tubules? J Physiol (Lond) 288:1–31
Frömter E (1982) Electrophysiological analysis of rat renal sugar and amino acid transport. 1. Basic phenomena. Pfluegers Arch 393:179–184
Frömter E, Diamond J (1972) Route of passive ion permeation in epithelia. Nature 235:9–13
Frömter E, Gessner K (1975) Effect of inhibitors and diuretics on electrical potential differences in rat kidney proximal tubule. Pfluegers Arch 357:209–224
Fujimoto M, Honda M (1980) Direct measurement of intracellular Na and K activities in the renal tubular cells with triple-barreled microelectrodes. Proc Int Congr Physiol Sci 14:119
Garay RP, Garrahan PJ (1973) The interaction of sodium and potassium with the sodium pump in red cells. J Physiol (Lond) 231:297–325
Gerencser GA, White JF (1980) Membrane potentials and chloride activities in epithelial cells of Aplysia intestine. Am J Physiol 239:R445-R449
Giebisch G (1968) Some electrical properties of single renal tubule cells. J Gen Physiol 51:315s
Gilles-Baillien M, Schoffeniels E (1965) Site of action of L-alanine and D-glucose on the potential difference across the intestine. Arch Int Physiol Biochim 73:355–357
Gunter-Smith PJ, Grasset E, Schultz SG (1982) Sodium-coupled amino acid and sugar transport by Necturus small intestine. An equivalent electrical circuit analysis of a rheogenic co-transport system. J Membr Biol 66:25–40
Kimura G, Spring KR (1979) Luminal Na+ entry into Necturus proximal tubule cells. Am J Physiol 236:F295-F307
Knight AB, Welt LG (1974) Intracellular potassium. A determinant of the sodium-potassium pump rate. J Gen Physiol 63:351–373
Koopman W, Schultz SG (1969) The effect of sugars and amino acids on mucosal Na+ and K+ concentrations in rabbit ileum. Biochim Biophys Acta 173:338–340
Kotera K, Satake N, Honda M, Fujimoto M (1979) The measurement of intracellular sodium activities in the bullfrog by means of double-barreled sodium liquid ion-exchanger microelectrodes. Membr Biochem 2:323–338
Lee CO, Armstrong WMcD (1972) Activities of sodium and potassium ions in epithelial cells of small intestine. Science 175:1261–1264
Nagel W, Garcia-Diaz JF, Armstrong WMcD (1981) Intracellular ionic acitivities in frog skin. J Membr Biol 61:127–134
Newey H, Parsons BJ, Smyth DH (1959) The site of action of phlorizin in inhibiting intestinal absorption of glucose. J Physiol (Lond) 148:83–92
O’Doherty J, Stark RJ (1981) Transmembrane and transepithelial movement of calcium during stimulus-secretion coupling. Am J Physiol 241:G150-G158
O’Doherty J, Garcia-Diaz JF, Armstrong WMcD (1979) Sodium-selective liquid ion-exchanger microelectrodes for intracellular measurements. Science 203:1349–1351
Okada Y, Sato T, Inouye A (1975) Effects of potassium ions and sodium ions on membrane potential of epithelial cells in rat duodenum. Biochim Biophys Acta 413:104–115
Okada Y, Iramajiri A, Inouye A (1976) Intracellular ion concentrations of epithelial cells in rat small intestine. Effects of external potassium ions and uphill transports of glucose and glycine. Jpn J Physiol 26:427–440
Okada Y, Tsuchiya W, Iramajiri A, Inouye A (1977) Electrical properties and active solute transport in rat small intestine. I. Potential profile changes associated with sugar and amino acid transport. J Membr Biol 31:205–219
Okada Y, Iramajiri A, Tsuchiya W, Inouye A (1978) Contribution of an electrogenic sodium pump to the membrane potential in the intestinal epithelial cell. Jpn J Physiol 28:511–525
Post RL, Merritt CR, Konsolving CR, Albright CD (1960) Membrane adenosine triphosphatase as a participant in the active transport of sodium and potassium in the human erythrocyte. J Biol Chem 235:1796–1802
Reuss L, Weinmann SA (1979) Intracellular ionic activities and transmembrane electrochemical potential differences in gallbladder epithelium. J Membr Biol 49:345–362
Riklis E, Quastel JH (1958) Effects of cations on sugar absorption by isolated surviving guinea pig intestine. Can J Biochem Physiol 36:347–362
Rose RC, Schultz SG (1971) Studies on the electrical potential profile across rabbit ileum. Effects of sugars and amino acids on transmural and transmucosal electrical potential differences. J Gen Physiol 57:639–663
Schachter D, Britten JS (1961) Active transport of non-electrolytes and the potential gradients across intestinal segments in vitro. Fed Proc 20:137
Skou JC (1957) Influence of some cations on an adenosine triphosphatase from peripheral nerves. Biochim Biophys Acta 23:394–401
Steiner RA, Ochme M, Amman D, Simon W (1979) Neutral carrier sodium ion-selective microelectrode for intracellular studies. Anal Chem 51:351–353
White JF (1976) Intracellular potassium activities in Amphiuma small intestine. Am J Physiol 231:1214–1219
White JF, Armstrong WMcD (1971) Effect of transported solutes on membrane potentials in bullfrog small intestine. Am J Physiol 221:194–201
Wright EM (1966) The origin of the glucose dependent increase in the potential difference across the tortoise small intestine. J Physiol (Lond) 185:486–500
Zeuthen T, Wright EM (1981) Epithelial potassium transport: Tracer and electrophysiological studies in choroid plexus. J Membr Biol 60:105–128
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© 1983 Springer-Verlag Berlin Heidelberg
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White, J.F., Imon, M.A. (1983). Effect of Galactose on Intracellular Potential and Sodium Activity in Urodele Small Intestine. Evidence for Basolateral Electrogenic Transport. In: Gilles-Baillien, M., Gilles, R. (eds) Intestinal Transport. Proceedings in Life Sciences. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69109-6_22
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DOI: https://doi.org/10.1007/978-3-642-69109-6_22
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