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  • 1990-1994  (2)
  • Diethyl maleate  (1)
  • Epicardial mapping  (1)
  • 1
    ISSN: 1438-2199
    Keywords: Amino acids ; N-Acetylcysteine ; Cysteine ; Glutathione ; Diethyl maleate ; Perfused rat liver
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Effect ofN-acetyl-l-cysteine (NAC) administration on cysteine and glutathione (GSH) contents in rat liver and kidney was studied using intact and diethyl maleate (DEM)-treated rats and perfused rat liver. Cysteine contents increased rapidly, reaching peak at 10 min after intraperitoneal NAC administration. In liver mitochondria it increased slowly, reaching peak at 60 min. GSH content did not change significantly in these tissues. However, in liver and kidney depleted of GSH with DEM, NAC administration restored GSH contents in 60 and 120 min, respectively. Perfusion with 10 mM NAC resulted in 76% increase in liver cysteine content, but not in GSH content. Liver perfusion of DEM-injected rats with 10 mM NAC restored GSH content by 15%. Present findings indicate that NAC is an effective precursor of cysteine in the intact liver and kidney and in the perfused rat liver, and that NAC stimulated GSH synthesis in GSH-depleted tissues.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 348 (1993), S. 643-649 
    ISSN: 1432-1912
    Keywords: Epicardial mapping ; Class-III-antiarrhythmic drugs ; Adrenoceptors ; Propranolol ; β-blockers ; Norepinephrine ; Dispersion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Isolated perfused spontaneously beating rabbit hearts were treated with increasing concentrations of norepinephrine (0.01, 0.1, 0.5 μmol/l) either alone or in presence of propranolol (0.1 μmol/l). For analysis of the epicardial activation and repolarization process and epicardial mapping (256 unipolar leads) was performed. For each electrode the activation and repolarization time was determined. From these data the “breakthrough-points” (BTP) of epicardial activation were determined. At each electrode an activation vector (VEC) was calculated giving direction and velocity of the local excitation wave. The beat similarity of various heart beats (under NE) compared to control was evaluated by determination of the percentage of identical BTP and of similar VEC (deviation ≤5°). Moreover at each electrode the local activation recovery interval (ARI) and its standard deviation (of 256 leads, dispersion, DISP) were determined. Norepinephrine alone (0.01, 0.1, 0.5 μmol/l) led to an increase in left ventricular pressure, heart rate and DISP with concomittant frequency dependent reduction in ARI, and to changes in the epicardial activation pattern (reduction in BTP, VEC). We found that in the presence of propranolol (0.1 μmol/l) norepinephrine prolonged ARI and reduced ARI-dispersion. This effect was not due to changes in heart rate. The disturbing effects on the activation pattern were dimished. These effects could be prevented by pretreatment with 1 μmol/l prazosine. From these results we conclude, that norepinephrine prolongs the relative action potential duration via stimulation of α1-adrenoceptor and enhances cellular coupling. Thus, the antiarrhythmic properties of propranolol may at least in part be due to an unmasking of class III like norepinephrine effects and additional reduction in dispersion.
    Type of Medium: Electronic Resource
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