Literature DB >> 6651779

A kinetic investigation of the effects of adrenaline on 45Ca2+ exchange in isolated hepatocytes at different Ca2+ concentrations, at 20 degrees C and in the presence of inhibitors of mitochondrial Ca2+ transport.

J C Parker, G J Barritt, J C Wadsworth.   

Abstract

The effects of adrenaline on 45Ca2+-exchange curves for isolated hepatocytes incubated under various steady-state conditions were investigated. Kinetic analysis showed that the simplest compartment configuration consistent with each set of data was a series configuration of a three-compartment closed system comprising compartment 1 (C1), the extracellular medium, and two kinetically distinct compartments of cellular exchangeable Ca2+, C2 and C3 (C1 = C2 = C3). Subcellular fractionation of hepatocytes labelled with 45Ca2+ at 0.1 mM-Ca2+ indicated that C3 includes exchangeable Ca2+ in the mitochondria and endoplasmic reticulum. The following results were obtained from experiments conducted at 37 degrees C at five different extracellular Ca2+ concentrations. For both untreated and adrenaline-treated cells, plots of the flux from C1 to C2 as a function of the extracellular Ca2+ concentration were best described by straight lines consistent with Ca2+ influx across the plasma membrane being a diffusion process. Adrenaline increased the value of the permeability constant for Ca2+ influx by 40%. For untreated cells, plots of the flux between C2 and C3 as a function of the concentrations of Ca2+ in these compartments approached a plateau at high Ca2+ concentrations. Adrenaline caused a 3-fold increase in the concentration of Ca2+ that gives half-maximal rate of Ca2+ transport from C2 to C3. At 1.3 mM extracellular Ca2+, a decrease in incubation temperature from 37 degrees C to 20 degrees C decreased the quantity of Ca2+ in C3 and the flux and fractional transfer rates for the transport of Ca2+ between C2 and C3. At 20 degrees C adrenaline increased the quantity of Ca2+ in C3 and the fractional transfer rates for the transfer of Ca2+ from C1 to C2, and from C2 to C3. At 37 degrees C and 2.4 mM extracellular Ca2+, antimycin A plus oligomycin decreased the quantity of Ca2+ in C3 and increased the fractional transfer rate for the transport of Ca2+ from C3 to C2. In the presence of antimycin A and oligomycin, adrenaline did not increase the quantity of Ca2+ in C2 or the flux and fractional transfer rate for the transport of Ca2+ from C1 to C2, whereas these parameters were increased in the absence of the inhibitors.

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Year:  1983        PMID: 6651779      PMCID: PMC1152469          DOI: 10.1042/bj2160051

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  63 in total

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Journal:  J Biol Chem       Date:  1973-08-10       Impact factor: 5.157

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Authors:  M Claret; J L Mazet
Journal:  J Physiol       Date:  1972-06       Impact factor: 5.182

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Authors:  P F Baker; A L Hodgkin; E B Ridgway
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8.  Effects of noradrenaline on potassium reflux, membrane potential and electrolyte levels in tissue slices prepared from guinea-pig liver.

Authors:  D G Haylett; D H Jenkinson
Journal:  J Physiol       Date:  1972-09       Impact factor: 5.182

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  6 in total

1.  Effects of vasopressin and La3+ on plasma-membrane Ca2+ inflow and Ca2+ disposition in isolated hepatocytes. Evidence that vasopressin inhibits Ca2+ disposition.

Authors:  B P Hughes; S E Milton; G J Barritt
Journal:  Biochem J       Date:  1986-09-15       Impact factor: 3.857

2.  The stimulation by sodium fluoride of plasma-membrane Ca2+ inflow in isolated hepatocytes. Evidence that a GTP-binding regulatory protein is involved in the hormonal stimulation of Ca2+ inflow.

Authors:  B P Hughes; G J Barritt
Journal:  Biochem J       Date:  1987-07-01       Impact factor: 3.857

3.  The liver cell plasma membrane Ca2+ inflow systems exhibit a broad specificity for divalent metal ions.

Authors:  J N Crofts; G J Barritt
Journal:  Biochem J       Date:  1990-08-01       Impact factor: 3.857

4.  The measurement of Ca2+ inflow across the liver cell plasma membrane by using quin2 and studies of the roles of Na+ and extracellular Ca2+ in the mechanism of Ca2+ inflow.

Authors:  J N Crofts; G J Barritt
Journal:  Biochem J       Date:  1989-11-15       Impact factor: 3.857

5.  Noradrenaline, vasopressin and angiotensin increase Ca2+ influx by opening a common pool of Ca2+ channels in isolated rat liver cells.

Authors:  J P Mauger; J Poggioli; F Guesdon; M Claret
Journal:  Biochem J       Date:  1984-07-01       Impact factor: 3.857

6.  Effects of lysophospholipids on Ca2+ transport in rat liver mitochondria incubated at physiological Ca2+ concentrations in the presence of Mg2+, phosphate and ATP at 37 degrees C.

Authors:  S Dalton; B P Hughes; G J Barritt
Journal:  Biochem J       Date:  1984-12-01       Impact factor: 3.857

  6 in total

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