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Biomedical subjects

S G Schultz

Publications and source records attributed to S G Schultz.

At least 91 records · Page 5Linked to original sources

Effects of unilateral sodium replacement on sugar transport across in vitro rabbit ileum.

The effects of unilateral sodium replacement with either choline or mannitol on passive and active 3-O-methyl-D-glucose (3-MG) absorption by in vitro rabbit ileum were examined. The results indicate that the predominant factor influencing 3-MG absorption is the presence of sodium in the mucosal bathing solution. Replacement of sodium in the mucosal solution alone markedly inhibits passive and essentially abolishes active 3-MG absorption regardless of the presence or absence of sodium in the serosal bathing solution. The presence or absence of sodium in the serosal solution does not affect transmural 3-MG transport regardless of the sodium concentration in the mucosal solution. Further, when sodium is replaced in the mucosal solution alone, the bidirectional transmural fluxes of 3-MG do not differ markedly from those of D-mannitol, a solute whose transport is probably attributable to simple diffusion. The present findings together with those of previous studies (15, 16) are consistent with the notion that replacement of sodium in the mucosal solution alone essentially abolishes transcellular 3-MG transport and that the remaining transepithelial fluxes are largely due to diffusion through the paracellular or shunt pathway. The relation of these findings to in vivo and in vitro studies in which perfusion of a segment of small intestine with a Na-free solution disclosed little or no inhibition of sugar absorption is discussed.

Animals↗

Effect of acetazolamide on sodium and chloride transport by in vitro rabbit ileum.

Acetazolamide (8 mM) aboishes active Cl absorption and inhibits but does not abolish active Na absorption by stripped, short-circuited rabbit ileum. These effects are not accompanied by significant changes in the transmural electrical potential difference or short-circuit current. Studies of the undirectional influxes of Na andCl indicate that acetazolamide inhibits the neutral, coupled NaCl influx process at the mucosal membranes. This action appears to explain the observed effect of acetazolamide on active, transepithelial Na and Cl transport. Acetazolamide did not significantly inhibit either spontaneous or theophylline-induced Cl secretion by this preparation, suggesting that the theophylline-induced secretion may not simply be due tothe unmasking of a preexisting efflux process when the neutral influx mechanism is inhibited by theophylline. Finally, inhibition of the neutral NaCl influx process by acetazolamide does not appear to be attributable to an inhibition of endogenous HCO3production or an elevation in intracellular cyclic-AMP levels. Instead, it appearstheat the effect of acetazolamide is due to a direct interaction with a membrane component involved in the coupled influx process.

Acetazolamide↗

Ionic conductances of extracellular shunt pathway in rabbit ileum. Influence of shunt on transmural sodium transport and electrical potential differences.

The unidirectional influxes of Na, K, and Cl into isolated strips of rabbit ileum are comprised of movements across the mucosal membrane of the epithelial cells and ionic diffusion into an extracellular shunt pathway. A large fraction of the Na influx across the mucosal membrane alone is inhibited by Li, suggesting the participation of a carrier mechanism in the influx process. The partial ionic shunt conductances of Na, K, and Cl account for at least 82% of the total tissue conductance. The calculated shunt permeabilities (P) are (in centimeters per hour) P(K) = 0.040, P(Na) = 0.035, and P(Cl) = 0.019, so that P(K):P(Na):P(Cl) = 1.14:1.00:0.55. Diffusion potentials across the tissue resulting from isotonic replacement of NaCl in the mucosal solution with mannitol or KCl are described by the Goldman constant-field equation together with the above permeabilities of the shunt pathway. These observations are not consistent with permeation through a fixed-charge pore but can be explained by a model featuring constant ionic partition into a neutral-polar pore that traverses the tight junction. Such a pore may be lined with either fixed dipoles or fixed dipolar ions oriented such that electronegative groups influence the permselective properties of the diffusion pathway. The essential feature of both models is that electroneutrality is maintained by means of fixed membrane components and does not depend upon the presence of mobile counterions.

Animals↗