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Am J Physiol Gastrointest Liver Physiol 256: G563-G569, 1989;
0193-1857/89 $5.00
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AJP - Gastrointestinal and Liver Physiology, Vol 256, Issue 3 563-G569, Copyright © 1989 by American Physiological Society


ARTICLES

Effect of hypertonic stress on liver cell volume, bile flow, and volume-regulatory K+ fluxes

P. Haddad, T. Thalhammer and J. Graf
Institute of General and Experimental Pathology, University of Vienna, Austria.

Net hepatic uptake and release of K+ were studied in the isolated-perfused rat liver subjected to a 10-min period of hyperosmotic stress by addition of 80 mM mannitol or sucrose to the perfusing solution. Bile flow and effluent Na+, K+, and Ca2+ activities were monitored throughout. Upon initiation of hypertonic stress, a sharp transient dilution of effluent ion activities indicated hepatic water losses that were larger and occurred more rapidly with sucrose than with mannitol. During continuous hyperosmotic perfusion, portocaval differences in K+ uncovered a steady net influx of the ion into the liver that reached a higher maximum and led to a greater accumulation in experiments with sucrose compared with mannitol. This hepatic K+ uptake was completely blocked by 1 mM ouabain. Upon return to isotonic conditions, a sharp transient concentration of effluent ion activities suggested hepatic water uptake that was again more rapid and pronounced in sucrose- than mannitol-treated livers. This was followed by a transient phase of net hepatic K+ release whose magnitude and duration were proportional to the water movements induced by the removal of each carbohydrate. Administration of 2 mM Ba2+ abolished this K+ efflux. These results indicate that mannitol equilibrates between extra- and intracellular compartments, whereas sucrose apparently does not. The data also suggest that net movements of K+ may be involved in the regulatory volume responses induced by hyperosmotic stress and return to normal tonicity, respectively.


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Am. J. Physiol. Gastrointest. Liver Physiol.Home page
C. E. Hill and J. E. Jacques
Cholestatic effects of the K+ channel blockers Ba2+ and TEA occur through different pathways in the rat liver
Am J Physiol Gastrointest Liver Physiol, January 1, 1999; 276(1): G43 - G48.
[Abstract] [Full Text] [PDF]




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