Hypertonic Stress Increases the Na + Conductance of Rat Hepatocytes in Primary Culture

作者: F Wehner , H Sauer , R K Kinne

DOI: 10.1085/JGP.105.4.507

关键词: ChemistryPatch clampOsmotic concentrationATPaseOsmoleHypertonic StressBiophysicsHepatocyteNa+/K+-ATPaseAmilorideBiochemistry

摘要: We studied the ionic mechanisms underlying regulatory volume increase of rat hepatocytes in primary culture by use confocal laser scanning microscopy, conventional and ion-sensitive microelectrodes, cable analysis, microfluorometry, measurements 86Rb+ uptake. Increasing osmolarity from 300 to 400 mosm/liter addition sucrose decreased cell volumes 88.6% within 1 min; thereafter, increased 94.1% control 10 min, equivalent a (RVI) 44.5%. This RVI was paralleled decrease input resistance specific membrane 88 60%, respectively. Ion substitution experiments (high K+, low Na+, Cl-) revealed that these effects are due an hepatocyte Na+ conductance. During RVI, ouabain-sensitive uptake augmented 141% control, K+ 148 180%, The increases conductance as well activation Na+/K(+)-ATPase were completely blocked 10(-5) mol/liter amiloride. At this concentration, amiloride had no effect on osmotically induced alkalinization via Na+/H+ exchange. When 220 (by readdition after preperiod 15 min which cells underwent decrease, RVD) initially 81.5%; thereafter 90.8% control. post-RVD-RVI 55.0% is also mediated conclude confluent capable post-RVD-RVI. In system, hypertonic stress leads considerable concert with conductive influx, then Na+/K(+)-ATPase. An additional role exchange regulation remains be defined.

参考文章(41)
A. Benedetti, M. Strazzabosco, J. G. Corasanti, P. Haddad, J. Graf, J. L. Boyer, Cl(-)-HCO3- exchanger in isolated rat hepatocytes: role in regulation of intracellular pH. American Journal of Physiology-gastrointestinal and Liver Physiology. ,vol. 261, ,(1991) , 10.1152/AJPGI.1991.261.3.G512
F. Lang, M. Ritter, H. Völkl, D. Häussinger, Cell Volume Regulatory Mechanisms — An Overview Advances in Comparative and Environmental Physiology. pp. 1- 31 ,(1993) , 10.1007/978-3-642-77124-8_1
D. Häussinger, W. Gerok, F. Lang, Cell Volume and Hepatic Metabolism Advances in Comparative and Environmental Physiology. pp. 33- 65 ,(1993) , 10.1007/978-3-642-77124-8_2
A. Lewis Farr, Oliver H. Lowry, Rose J. Randall, Nira J. Rosebrough, Protein Measurement with the Folin Phenol Reagent Journal of Biological Chemistry. ,vol. 193, pp. 265- 275 ,(1951)
R. M. Henderson, J. Graf, J. L. Boyer, Na-H exchange regulates intracellular pH in isolated rat hepatocyte couplets. American Journal of Physiology-gastrointestinal and Liver Physiology. ,vol. 252, ,(1987) , 10.1152/AJPGI.1987.252.1.G109
P. Haddad, J. Graf, Volume-regulatory K+ fluxes in the isolated perfused rat liver: characterization by ion transport inhibitors. American Journal of Physiology-gastrointestinal and Liver Physiology. ,vol. 257, ,(1989) , 10.1152/AJPGI.1989.257.3.G357
J. G. Corasanti, D. Gleeson, J. L. Boyer, Effects of osmotic stresses on isolated rat hepatocytes. I. Ionic mechanisms of cell volume regulation. American Journal of Physiology-gastrointestinal and Liver Physiology. ,vol. 258, ,(1990) , 10.1152/AJPGI.1990.258.2.G290
Kening Wang, Robert Wondergem, Effects of hyperosmotic medium on hepatocyte volume, transmembrane potential and intracellular K+ activity Biochimica et Biophysica Acta. ,vol. 1069, pp. 187- 196 ,(1991) , 10.1016/0005-2736(91)90123-P
E. Frömter, The route of passive ion movement through the epithelium of Necturus gallbladder. The Journal of Membrane Biology. ,vol. 8, pp. 259- 301 ,(1972) , 10.1007/BF01868106