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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 436 (1998), S. 384-390 
    ISSN: 1432-2013
    Keywords: Key words l-Alanine ; l-Glutamate ; Transport ; Sarcolemma ; Myocardial protection ; Heart cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  During cardiac insults, heart cells synthesise and accumulate alanine as a part of the anaerobic energy production pathway. The transport of alanine presumably influences this pathway, making it important to characterise the l-alanine transporter in the heart. In this study, we have investigated the transport of l-alanine across the sarcolemma using a novel approach, namely utilisation of two preparations: cardiac sarcolemmal vesicles and cardiac myocytes. Both preparations were isolated from the heart of the same mammalian species. l-Alanine uptake in both preparations was sodium dependent. In the sarcolemmal vesicles, the sodium dependent component was electrogenic and saturated with an estimated Michaelis-Menten constant (K m) and maximal reaction velocity (V max) of 0.48±0.18 mM and 279.97±64.17 pmol/mg per min respectively at room temperature. In the isolated myocytes, l-alanine uptake was linear in sodium-containing media, with an estimated K m and V max of 9.65±0.76 mM and 169.81±13.22 pmol/µl per min respectively at 10°C for the sodium-dependent component. Inhibition of cotransport by a variety of substrates indicated that l-alanine uptake in the heart is mediated by an A- or ASC-like system. These characteristics of l-alanine transport suggest that under ischaemic conditions, l-alanine efflux will be activated, thus allowing for the continuous utilisation of other amino acids for energy production.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Key words Brush-border ; Membrane vesicle ; Cystic fibrosis transmembrane regulator (cftr) ; Alternate Cl ; conductance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstracts  Brush-border membrane vesicles (BBMV) were prepared from whole Balb/c mice kidneys by a Mg2+ precipitation technique. The presence of an intrinsic Cl–conductance co-expressed with Na+/glucose cotransport was inferred by the anion dependence of [14C]glucose uptake and overshoot with inward Na+-anion gradients. In Na+-equilibrated conditions, an inside-negative membrane potential difference (p.d.) produced by an inward Cl–gradient alone was capable of driving intravesicular [14C]glucose accumulation. The apparent anion conductance had a selectivity of Br– = I– = Cl– 〉  F–〉〉 gluconate, was inhibited by 0.5 mM 5-nitro-2- (3-phenylpropylamino)-benzoic acid (NPPB) but was unaffected by 0.5 mM 4,4′-diisothiocyanatostilbene 2,2′-disulphonate (DIDS). BBMV were isolated from mice in which the CFTR gene had been disrupted by a termination mutation (–/–) and compared with normal litter mates (+/+) and heterozygotes (–/+)[18]. [14C]Glucose uptake in NaCl media was significantly greater than glucose uptake in Na gluconate media for all three genotypes measured at 20 s: for homozygous –/– animals [14C]glucose uptake was increased by 2.80 ± 0.53 fold in Cl–media compared to gluconate media, n = 6; for wild-type +/+, by 2.16 ± 0.53 fold, n = 8; and for heterozygous +/– animals, by 2.17 ± 0.45 fold, n = 8. The observation of a Cl–-dependent component in BBMV isolated from homozygous –/– mutant animals shows that the chloride conductance in these vesicles cannot be due to cftr expression.
    Type of Medium: Electronic Resource
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