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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 779 (1996), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Rabbit heart ; Alpha-adrenoceptors ; Potassium currents ; Protein kinase C
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The selective α1-adrenergic agonist methoxamine (10−4–10−3M), in the presence of propranolol (10−6M), can reduce both the inwardly rectifying K+ background current (I K1) and the muscarinic cholinergic receptor-activated K+ current (I K, ACh) in rabbit atrial myocytes resulting in action potential prolongation during the final phase of repolarization and a depolarization of the resting membrane potential. The reduction of these K+ current(s) by α1-adrenoceptor stimulation was insensitive to pre-treatment of artial myocytes with pertussis toxin (0.15–0.5 μg/ml) and was irreversible following intracellular dialysis with the non-hydrolysable guanosine triphosphate (GTP) analogue, Gpp(NH)p (1−5×10−3M). Neither the protein kinase C (PKC) inhibitors, 1-(5-isoquinolinesulphonyl)-2-methylpiperoxine (H-7) (5×10−5M) and staurosporine (1×10−7M), nor “downregulation” of PKC by prolonged phorbol ester exposure (5×10−7M, for 7–8 h) had an effect on the α1-adrenergic modulation of this K+ current. Under cellattached patch-clamp conditions, bath application of methoxamine reversibly decreased acetylcholine-induced single-channel activity, thus confirming the observed reduction of the ACh-induced current under whole-cell voltage clamp. These results demonstrate that the α1adrenoceptor, once activated, can reduce current through two different inwardly rectifying K+ channels in rabbit atrial myocytes. These current changes are mediated via a pertussis toxin-insensitive GTP-binding protein, and do not appear to involve the activation of PKC.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1424
    Keywords: atrium ; sinus venosus ; pacemaker ; inward rectifier ; impedance ; isolated cardiac cells ; linear analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Single electrode whole cell voltage-clamp experiments and frequency domain analyses have been used to study and compare the K+ currents in enzymatically dispersed single cells from the atrium and the sinus venosus (pacemaker region) of the bullfrog heart. Admittance measurements made near the ‘resting’ or zero-current potential yield data from which the equivalent circuit of each cell type may be obtained. Data from both atrial and pacemaker cells are well-fitted by a model consisting only of parallel resistance-capacitative elements, as predicted from their micro-anatomy. Neither of these amphibian cardiac cells contain a transverse tubule system (TT) and both have very little sarcoplasmic reticulum (SR). These results complement and extend two earlier investigations: (i) Moore, Schmid and Isenberg (J. Membrane Biol. 81:29–40, 1984) have reported that in guinea pig ventricle cells (whichdo contain an internal membrane system consisting of transverse tubules and a substantial SR) the SR may be electrically coupled to the sarcolemma; (ii) Shibata and Giles (Biophys. J. 45:136a, 1984) have shown that although bullfrog atrial cells have an inwardly rectifying back-ground K+ current, $$I_{K_1 } $$ , pacemaker cells from the immediately adjacent sinus venosus do not. Data from admittance measurements also provide evidence that a TTX-insensitive inward Ca2+ current is activated in the pacemaker range of potentials.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Annals of biomedical engineering 28 (2000), S. 951-957 
    ISSN: 1573-9686
    Keywords: Action potential conduction ; Computer modeling ; Inward rectification ; Cable equations ; Hyperkalemia ; Ischemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract We have studied the dependence of conduction velocity (θ) on extracellular potassium concentration ([K+]o) in a model of one-dimensional conduction using an idealized strand of human atrial cells. Elevated [K+]o in the 5–20 mM range shifts the resting potential (V rest) in the depolarizing direction and reduces input resistance (R in) by increasing an inwardly rectifying K+ conductance, I Kl.Our results show that in this model: (1) θ depends on [K+] in a “biphasic” fashion. Moderate elevations of [K+]o (to less than 8 mM) result in a small increase in θ, whereas at higher [K+]o (8–16 mM) θ is reduced. (2) This biphasic relationship can be attributed to the competing effects of (i) the smaller depolarization needed to reach the excitation threshold (V thresh-V rest) and (ii) reduced availability (increased inactivation) of sodium current, I Na, as the cell depolarizes progressively. (3) Decreasing R in reduces θ due to the increased electrical load on surrounding cells. (4) The effect on θ of [K+]o-induced changes in R inin the atrium (as well as other high-R in tissue, such as that of the Purkinje system or nodes) is likely to be small. This effect could be substantial, however, under conditions in which R in is comparable in size to gap junction resistance and membrane resistance (inverse slope of the whole-cell current–voltage relationship) when sodium channels are open, which is likely to be the case in ventricular tissue. © 2000 Biomedical Engineering Society.PAC00: 8716Uv, 8719Hh, 8716Ac
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Annals of biomedical engineering 28 (2000), S. 958-967 
    ISSN: 1573-9686
    Keywords: Mouse heart ; Electrocardiogram ; Voltage–sensitive dye ; Anisotropic conduction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract A custom-made apparatus based on a charge-coupled-device camera has been used to monitor changes in fluorescence from Langendorff-perfused adult mouse hearts stained with a voltage-sensitive dye, di-4-ANEPPS. With this approach it is possible to monitor activation of the ventricles at high temporal (375 μs/frame) and spatial resolution 72 × 78pixels,100 ×100 μm/pixel. In sinus rhythm, activation occurred with a complicated breakthrough pattern on both ventricles, and a total activation time of 3.51 ± 0.16ms (32 °C). A stimulus applied near the apex of the left ventricle resulted in a single activation wave front with a total activation time of 8.18 ± 0.25 ms. Pacing from a site near the middle of the left ventricular epicardial surface revealed anisotropic conduction, indicating that conduction occurs preferentially in the direction of the predominant fiber orientation. The total activation time in this configuration was 5.44 ± 0.24 ms. The difference in total activation time between sinus rhythm and epicardial stimulation suggests an important role for transmural conduction (the Purkinje system) in the mouse heart. These findings provide much of the necessary background needed for studying conduction abnormalities in genetically altered mice and suggest that the comparison of sinus rhythm and epicardial pacing can be used to reveal transmural conduction abnormalities. © 2000 Biomedical Engineering Society. PAC00: 8719Nn, 8719Hh, 8716Uv, 8764Ni
    Type of Medium: Electronic Resource
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