Unlabelled: The model of sodium and chloride transport proposed for the colon is based on studies performed in the distal segment and tacitly assumes that ion transport is similar throughout the colon. In rat distal colon, neutral sodium-chloride absorption accounts for the major fraction of overall sodium absorption and aldosterone stimulates electrogenic, amiloride-sensitive sodium absorption. Since we have demonstrated qualitative differences in potassium transport in proximal and distal segments of rat colon, unidirectional 22Na and 36Cl fluxes were performed under short-circuit conditions across isolated proximal colon of control and sodium-depleted rats with secondary hyperaldosteronism. In the control group, net sodium absorption (JNanet) (7.4 +/- 0.5 mu eq/h . cm2) was greater than Isc (1.4 +/- 0.1 mu eq/h . cm2), and JClnet was 0 in Ringer solution. Residual flux (JR) was -5.2 +/- 0.5 mu eq/h . cm2 consistent with hydrogen ion secretion suggesting that neutral sodium absorption may represent sodium-hydrogen exchange. 1 mM mucosal amiloride, which inhibits sodium-hydrogen exchange in other epithelia, produced comparable decreases in JNanet and JR (4.1 +/- 0.6 and 3.2 +/- 0.6 mu eq/h . cm2, respectively) without a parallel fall in Isc. Sodium depletion stimulated JNanet, JClnet, and Isc by 7.0 +/- 1.4, 6.3 +/- 1.9, and 0.8 +/- 0.2 mu eq/h . cm2, respectively, and 1 mM amiloride markedly inhibited JNanet and JClnet by 6.0 +/- 1.1 and 4.0 +/- 1.6 mu eq/h . cm2, respectively, with only a minimal reduction in Isc.
Conclusions: the predominant neutral sodium-absorptive mechanism in proximal colon is sodium-hydrogen exchange. Sodium depletion stimulates electroneutral chloride-dependent sodium absorption (most likely as a result of increasing sodium-hydrogen and chloride-bicarbonate exchanges), not electrogenic chloride-independent sodium transport. The model of ion transport in the proximal colon is distinct from that of the distal colon.
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http://dx.doi.org/10.1172/JCI112281 | DOI Listing |
Dalton Trans
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Max Planck Institute for Chemical Energy Conversion, Stiftstraße 34-36, D-45470 Mülheim an der Ruhr, Germany.
Aquo and hydroxo ligands play an essential role in the chemistry of many copper enzymes and small molecule catalysts. The formation of a series of copper complexes with HO and OH ligands in various positions, including [Cu(bpy)(OAc)(HO)] (Cu-I), [Cu(bpy)(OH)(HO)] (Cu-III), [Cu(OH)(HO)] (Cu-IV), [Cu(bpy)(HO)(HO)] (Cu-V) and [Cu(bpy)(HO)] (Cu-VI), were investigated through Electron Paramagnetic Resonance (EPR) and UV-Vis spectroscopy in aqueous copper bipyridine solutions in the dependence of the pH and the copper-to-bipyridine ratio (bpy = 2,2'-bipyridine). H- and O-enrichment of the copper complexes allowed us to determine the H and O nuclear hyperfine interactions of their HO ligands Q-band Electron Nuclear Double Resonance (ENDOR) spectroscopy.
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Chair of Urban Water Systems Engineering, Technical University of Munich, Am Coulombwall 3, Garching 85748, Germany.
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