Literature DB >> 2717371

Water, K+, H+, lactate and glucose fluxes during cell volume regulation in perfused rat liver.

F Lang1, T Stehle, D Häussinger.   

Abstract

The present study has been performed to test for ion release from isolated perfused rat liver exposed to hypotonic perfusates. Replacement of 40 mmol/l NaCl in perfusate by 80 mmol/l raffinose leads to slight alkalinization and slight decrease of liver weight. Subsequent decrease of perfusate osmolarity by omission of raffinose results in an increase of liver weight and a parallel increase of effluent sodium, chloride and potassium activity pointing to net uptake of solute free water. While effluent chloride and sodium activities approach perfusate activities within less than 2 min, a second, 6 min lasting increase of effluent potassium activity is observed, pointing to potassium release by the liver. This transient increase of effluent potassium activity is paralleled by a decrease of liver weight. Throughout exposure to hypotonic perfusates, lactate, pyruvate and glucose release by the liver is significantly decreased and effluent pH is rendered alkaline. Readdition of 80 mmol/l raffinose leads to rapid decrease of liver weight and a parallel decrease of effluent sodium, chloride and potassium activities followed by a 10-20 min lasting decrease of effluent potassium activity, pointing to net uptake of potassium, which almost matches the net release observed before. The transient decrease of potassium activity is paralleled by an increase of liver weight, an increase of effluent glucose, lactate and pyruvate concentration and an acidification of the effluent. Similar decrease of effluent potassium activity, acidification of effluent and increase of effluent glucose, lactate and pyruvate concentration are observed, if perfusates are made hypertonic by addition of raffinose.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2717371     DOI: 10.1007/BF00583532

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  41 in total

1.  Isolated perfused rat liver: an experimental model for studies on ammonium and amino acid metabolism.

Authors:  D Häussinger
Journal:  Infusionsther Klin Ernahr       Date:  1987-08

2.  Cellular aspects of renal sodium transport and cell volume regulation.

Authors:  G Whittembury; J J Grantham
Journal:  Kidney Int       Date:  1976-02       Impact factor: 10.612

3.  Volume regulation by Necturus gallbladder: basolateral KCl exit.

Authors:  M Larson; K R Spring
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

4.  Epithelial cell volume regulation in hypotonic fluids: studies using a model tissue culture renal epithelial cell system.

Authors:  N L Simmons
Journal:  Q J Exp Physiol       Date:  1984-01

5.  Epithelial cell volume regulation: bicarbonate dependence.

Authors:  R S Fisher; B E Persson; K R Spring
Journal:  Science       Date:  1981-12-18       Impact factor: 47.728

6.  Furosemide-sensitive Na+ and K+ transport and human erythrocyte volume.

Authors:  W C O'Neill; R B Mikkelsen
Journal:  Biochim Biophys Acta       Date:  1987-01-26

7.  Role of separate K+ and Cl- channels and of Na+/Cl- cotransport in volume regulation in Ehrlich cells.

Authors:  E K Hoffmann
Journal:  Fed Proc       Date:  1985-06

8.  Volume-regulatory K+ efflux during concentrative uptake of alanine in isolated rat hepatocytes.

Authors:  L O Kristensen; M Folke
Journal:  Biochem J       Date:  1984-07-01       Impact factor: 3.857

Review 9.  Associations between transports of alanine and cations across cell membrane in rat hepatocytes.

Authors:  L O Kristensen
Journal:  Am J Physiol       Date:  1986-11

10.  Regulatory volume decrease in perfused proximal nephron: evidence for a dumping of cell K+.

Authors:  K L Kirk; D R DiBona; J A Schafer
Journal:  Am J Physiol       Date:  1987-05
View more
  35 in total

Review 1.  Hepatic encephalopathy as a complication of liver disease.

Authors:  S vom Dahl; G Kircheis; D Häussinger
Journal:  World J Gastroenterol       Date:  2001-04       Impact factor: 5.742

2.  Cell shrinkage follows, rather than mediates, the short-term effects of glucagon on carbohydrate metabolism.

Authors:  V Gaussin; A Baquet; L Hue
Journal:  Biochem J       Date:  1992-10-01       Impact factor: 3.857

3.  Cell swelling increases bile flow and taurocholate excretion into bile in isolated perfused rat liver.

Authors:  C Hallbrucker; F Lang; W Gerok; D Häussinger
Journal:  Biochem J       Date:  1992-02-01       Impact factor: 3.857

4.  Further characterization of volume regulatory decrease in cultured renal epitheloid (MDCK) cells.

Authors:  M Ritter; M Paulmichl; F Lang
Journal:  Pflugers Arch       Date:  1991-03       Impact factor: 3.657

5.  What determines the increase in liver cell volume in the fasted-to-fed transition: glycogen or insulin?

Authors:  L Agius; M Peak; M al-Habori
Journal:  Biochem J       Date:  1991-06-15       Impact factor: 3.857

6.  Swelling of rat hepatocytes activates acetyl-CoA carboxylase in parallel to glycogen synthase.

Authors:  A Baquet; L Maisin; L Hue
Journal:  Biochem J       Date:  1991-09-15       Impact factor: 3.857

7.  Cell swelling inhibits proteolysis in perfused rat liver.

Authors:  D Häussinger; C Hallbrucker; S vom Dahl; F Lang; W Gerok
Journal:  Biochem J       Date:  1990-11-15       Impact factor: 3.857

8.  Modification of liver cell volume by insulin and glucagon.

Authors:  C Hallbrucker; S vom Dahl; F Lang; W Gerok; D Häussinger
Journal:  Pflugers Arch       Date:  1991-06       Impact factor: 3.657

9.  Properties of a cell volume-sensitive potassium conductance in isolated guinea-pig and rat hepatocytes.

Authors:  C A Sandford; J H Sweiry; D H Jenkinson
Journal:  J Physiol       Date:  1992-02       Impact factor: 5.182

10.  SGK1 dependence of insulin induced hypokalemia.

Authors:  Krishna M Boini; Dirk Graf; Dietmar Kuhl; Dieter Häussinger; Florian Lang
Journal:  Pflugers Arch       Date:  2008-07-30       Impact factor: 3.657

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.