Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
J Physiol
2001 Mar 15;531Pt 3:631-44. doi: 10.1111/j.1469-7793.2001.0631h.x.
Show Gene links
Show Anatomy links
Isotonic transport by the Na+-glucose cotransporter SGLT1 from humans and rabbit.
Zeuthen T
,
Meinild AK
,
Loo DD
,
Wright EM
,
Klaerke DA
.
???displayArticle.abstract???
1. In order to study its role in steady state water transport, the Na+-glucose cotransporter (SGLT1) was expressed in Xenopus laevis oocytes; both the human and the rabbit clones were tested. The transport activity was monitored as a clamp current and the flux of water followed optically as the change in oocyte volume. 2. SGLT1 has two modes of water transport. First, it acts as a molecular water pump: for each 2 Na+ and 1 sugar molecule 264 water molecules were cotransported in the human SGLT1 (hSGLT1), 424 for the rabbit SGLT1 (rSGLT1). Second, it acts as a water channel. 3. The cotransport of water was tightly coupled to the sugar-induced clamp current. Instantaneous changes in clamp current induced by changes in clamp voltage were accompanied by instantaneous changes in the rate of water transport. 4. The cotransported solution was predicted to be hypertonic, and an osmotic gradient built up across the oocyte membrane with continued transport; this resulted in an additional osmotic influx of water. After 5-10 min a steady state was achieved in which the total influx was predicted to be isotonic with the intracellular solution. 5. With the given expression levels, the steady state water transport was divided about equally between cotransport, osmosis across the SGLT1 and osmosis across the native oocyte membrane. 6. Coexpression of AQP1 with the SGLT1 increased the water permeability more than 10-fold and steady state isotonic transport was achieved after less than 2 s of sugar activation. One-third of the water was cotransported, and the remainder was osmotically driven through the AQP1. 7. The data suggest that SGLT1 has three roles in isotonic water transport: it cotransports water directly, it supplies a passive pathway for osmotic water transport, and it generates an osmotic driving force that can be employed by other pathways, for example aquaporins.
Borgnia,
Cellular and molecular biology of the aquaporin water channels.
1999, Pubmed
Borgnia,
Cellular and molecular biology of the aquaporin water channels.
1999,
Pubmed
Carpi-Medina,
Diffusive water permeability in isolated kidney proximal tubular cells: nature of the cellular water pathways.
1988,
Pubmed
Dainty,
Unstirred layers in frog skin.
1966,
Pubmed
Dempster,
Glucose transporters do not serve as water channels in renal and intestinal epithelia.
1991,
Pubmed
Gonzáles,
Osmotic water permeability of the apical membrane of proximal straight tubular (PST) cells.
1984,
Pubmed
Green,
Luminal hypotonicity: a driving force for fluid absorption from the proximal tubule.
1984,
Pubmed
Hediger,
Homology of the human intestinal Na+/glucose and Escherichia coli Na+/proline cotransporters.
1989,
Pubmed
Loike,
Sodium-glucose cotransporters display sodium- and phlorizin-dependent water permeability.
1996,
Pubmed
,
Xenbase
Loo,
Passive water and ion transport by cotransporters.
1999,
Pubmed
,
Xenbase
Loo,
Relaxation kinetics of the Na+/glucose cotransporter.
1993,
Pubmed
,
Xenbase
Loo,
Cotransport of water by the Na+/glucose cotransporter.
1996,
Pubmed
,
Xenbase
MacAulay,
Water transport by the human Na+-coupled glutamate cotransporter expressed in Xenopus oocytes.
2001,
Pubmed
,
Xenbase
Mackenzie,
Relationships between Na+/glucose cotransporter (SGLT1) currents and fluxes.
1998,
Pubmed
,
Xenbase
Meinild,
The human Na+-glucose cotransporter is a molecular water pump.
1998,
Pubmed
,
Xenbase
Meinild,
Bidirectional water fluxes and specificity for small hydrophilic molecules in aquaporins 0-5.
1998,
Pubmed
,
Xenbase
Meinild,
Water transport by the renal Na(+)-dicarboxylate cotransporter.
2000,
Pubmed
,
Xenbase
Pappenheimer,
Contribution of solvent drag through intercellular junctions to absorption of nutrients by the small intestine of the rat.
1987,
Pubmed
Parent,
Electrogenic properties of the cloned Na+/glucose cotransporter: I. Voltage-clamp studies.
1992,
Pubmed
,
Xenbase
Pratz,
Osmotic water permeability and solute reflection coefficients of rat kidney brush-border membrane vesicles.
1986,
Pubmed
Schnermann,
Defective proximal tubular fluid reabsorption in transgenic aquaporin-1 null mice.
1998,
Pubmed
Soreq,
Xenopus oocyte microinjection: from gene to protein.
1992,
Pubmed
,
Xenbase
Vallon,
Luminal hypotonicity in proximal tubules of aquaporin-1-knockout mice.
2000,
Pubmed
van Heeswijk,
Osmotic water permeabilities of brush border and basolateral membrane vesicles from rat renal cortex and small intestine.
1986,
Pubmed
Verkman,
Water permeability and fluidity of renal basolateral membranes.
1986,
Pubmed
Verkman,
Lessons on renal physiology from transgenic mice lacking aquaporin water channels.
1999,
Pubmed
Worman,
Osmotic water permeability of small intestinal brush-border membranes.
1985,
Pubmed
Wright,
Structure and function of the Na+/glucose cotransporter.
1998,
Pubmed
,
Xenbase
Zampighi,
A method for determining the unitary functional capacity of cloned channels and transporters expressed in Xenopus laevis oocytes.
1995,
Pubmed
,
Xenbase
Zeuthen,
Water transport by the Na+/glucose cotransporter under isotonic conditions.
1997,
Pubmed
,
Xenbase
Zeuthen,
Cotransport of H+, lactate and H2O by membrane proteins in retinal pigment epithelium of bullfrog.
1996,
Pubmed
Zeuthen,
Molecular water pumps.
2000,
Pubmed
,
Xenbase
Zeuthen,
Cotransport of K+, Cl- and H2O by membrane proteins from choroid plexus epithelium of Necturus maculosus.
1994,
Pubmed
Zeuthen,
Secondary active transport of water across ventricular cell membrane of choroid plexus epithelium of Necturus maculosus.
1991,
Pubmed