Literature DB >> 731453

Cell membrane potential and resistance in liver.

J Graf, O H Petersen.   

Abstract

1. Isolated segments of mouse liver were placed in a Perspex bath through which physiological saline solutions of varying composition were circulated. Two microelectrodes were inserted in different liver cells under microscopic control allowing measurement of distance between the two micro-electrode tips. Current pulses were injected through one of these electrodes, causing electrotonic potential changes in nearby cells by current spread through intercellular junctions. These electrotonic potential changes were recorded with the second micro-electrode. The spatial decrement of the amplitude of the electrotonzpotential changes and their dependence on extracellular ion concentrations were analysed by three-dimensional cable analysis, modified to account for the geometry of the tissue. 2. During exposure to control solution the mean resting cell membrane potential was -37 mV, the space constant for intracellular current spread (lambda3 = square root of Rm/chrRi) was 390 micron and Ri, a measure which includes the intracellular resistivity and the junctional resistances, was 1.4 komegacm. From these values, and an estimate of tissue cell membrane density (chi) obtained by others, the specific membrane resistance (Rm) was calculated to be 5.1 komegacm2. 3. Replacement of extracellular Na+ by K+ resulted in a large depolarization and a large decrease in the membrane resistance. Replacement of extracellular Na+ by choline resulted in a small transient hyperpolarization and a small increase in the membrane resistance. Replacement of extracellular Cl- by methylsulphate or sulphate or of NaCl by sucrose resulted in a small transient depolarization and a large increase in the membrane resistance. 4. Glucagon (10(-7) M) and adrenaline (10(-5) M) evoked membrane hyperpolarization and reduction of membrane resistance (Rm). 5. The resting membrane ion conductance can be considered to consist of three components, Cl conductance (GCl), GK and GNa. The results suggest that GCl greater than GK greater than GNa. Changes in extracellular ion concentrations specifically alter the permeability properties of the cell membrane. The glucagon action can be explained in part by an increase in GK.

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Year:  1978        PMID: 731453      PMCID: PMC1282811          DOI: 10.1113/jphysiol.1978.sp012530

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  31 in total

1.  Electrical properties of the cellular transepithelial pathway in Necturus gallbladder. I. Circuit analysis and steady-state effects of mucosal solution ionic substitutions.

Authors:  L Reuss; A L Finn
Journal:  J Membr Biol       Date:  1975-12-04       Impact factor: 1.843

2.  Current flow and potential in a three-dimensional syncytium.

Authors:  R D Purves
Journal:  J Theor Biol       Date:  1976-07-21       Impact factor: 2.691

3.  Cyclic adenosine monophosphate, cyclic guanosine monophosphate, and glucagon: effects on membrane potential and ion fluxes in the liver.

Authors:  A P Somlyo; A V Somlyo; N Friedmann
Journal:  Ann N Y Acad Sci       Date:  1971-12-30       Impact factor: 5.691

4.  Membrane potential and resistance changes induced in salivary gland acinar cells by microiontophoretic application of acetylcholine and adrenergic agonists.

Authors:  M L Roberts; O H Petersen
Journal:  J Membr Biol       Date:  1978-03-20       Impact factor: 1.843

5.  Effect of ionic concentration changes on membrane potential of perfused rat liver.

Authors:  M Claret; E Coraboeuf; M P Favier
Journal:  Arch Int Physiol Biochim       Date:  1970-08

6.  Electrogenic sodium pump in mouse liver parenchymal cells.

Authors:  J Graf; O H Petersen
Journal:  Proc R Soc Lond B Biol Sci       Date:  1974-11-05

7.  Action potentials in the rat chromaffin cell and effects of acetylcholine.

Authors:  B L Brandt; S Hagiwara; Y Kidokoro; S Miyazaki
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

8.  Fracture faces of zonulae occludentes from "tight" and "leaky" epithelia.

Authors:  P Claude; D A Goodenough
Journal:  J Cell Biol       Date:  1973-08       Impact factor: 10.539

9.  Distribution of organelles and membranes between hepatocytes and nonhepatocytes in the rat liver parenchyma. A stereological study.

Authors:  A Blouin; R P Bolender; E R Weibel
Journal:  J Cell Biol       Date:  1977-02       Impact factor: 10.539

10.  Variations in tight and gap junctions in mammalian tissues.

Authors:  D S Friend; N B Gilula
Journal:  J Cell Biol       Date:  1972-06       Impact factor: 10.539

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  30 in total

1.  Editorial: cell biology of the hepatobiliary system.

Authors:  Renate Fuchs; Theresia Thalhammer
Journal:  Wien Med Wochenschr       Date:  2008

2.  Determination of cell membrane resistance in cultured renal epithelioid (MDCK) cells: effects of cadmium and mercury ions.

Authors:  M Ritter; F Lang; G Grübl; H G Embacher
Journal:  Pflugers Arch       Date:  1990-09       Impact factor: 3.657

Review 3.  Carrier-mediated transport in the hepatic distribution and elimination of drugs, with special reference to the category of organic cations.

Authors:  D K Meijer; W E Mol; M Müller; G Kurz
Journal:  J Pharmacokinet Biopharm       Date:  1990-02

4.  Hepatocyte gap junctions are permeable to the second messenger, inositol 1,4,5-trisphosphate, and to calcium ions.

Authors:  J C Sáez; J A Connor; D C Spray; M V Bennett
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

5.  Effect of intracellular pH on potassium conductance in liver.

Authors:  R M Henderson; B Krumpholz; J L Boyer; J Graf
Journal:  Pflugers Arch       Date:  1988-08       Impact factor: 3.657

6.  Cell membrane and transepithelial voltages and resistances in isolated rat hepatocyte couplets.

Authors:  J Graf; R M Henderson; B Krumpholz; J L Boyer
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

7.  Glucagon activates Ca2+ and Cl- channels in rat hepatocytes.

Authors:  Edoardo C Aromataris; Michael L Roberts; Greg J Barritt; Grigori Y Rychkov
Journal:  J Physiol       Date:  2006-03-31       Impact factor: 5.182

8.  Direct determination of the driving forces for taurocholate uptake into rat liver plasma membrane vesicles.

Authors:  M C Duffy; B L Blitzer; J L Boyer
Journal:  J Clin Invest       Date:  1983-10       Impact factor: 14.808

9.  Redistribution of hepatocyte chloride during L-alanine uptake.

Authors:  K Wang; R Wondergem
Journal:  J Membr Biol       Date:  1993-09       Impact factor: 1.843

10.  Isoprenaline- and noradrenaline-induced hyperpolarization of guinea-pig liver cells.

Authors:  T Karashima
Journal:  Br J Pharmacol       Date:  1981-08       Impact factor: 8.739

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