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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 301 (1978), S. 201-205 
    ISSN: 1432-1912
    Keywords: Phenylephrine ; α-Adrenoceptor ; Ca2+-dependent action potential ; Rabbit papillary muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Electrophysiological and mechanical effects of phenylephrine were observed in the rabbit papillary muscle which was depolarized and rendered inexcitable by an elevation of potassium concentration to 27 mM in the presence of a β-adrenoceptor blocking drug, bufetolol (10−6 M). 1. Phenylephrine (10−6 to 10−4 M) restored the action potential and tension development. The amplitude, duration and maximum rate of rise of the action potential, and developed tension were augmented by an increase in the concentration of phenylephrine. 2. The amplitude of the action potential restored by phenylephrine was very sensitive to the Ca2+ concentration and increased by 29.2 mV/10-fold increase crease in external Ca2+ concentration. Nifedipine (10−6 M), a Ca2+ antagonist, completely suppressed the electrical and mechanical responses restored by phenylephrine (10−5 M), but tetrodotoxin (10−5 M) had little effect on these responses. 3. Phentolamine (10−6 M) suppressed both the action potential and developed tension restored by phenylephrine (10−5 M), but the elevation of the concentration of bufetolol from 10−6 M to 3×10−6 M was ineffective against these responses. In conclusion, the restoration by phenylephrine of Ca2+-dependent action potential may be ascribed to an enhancement of the inward Ca2+ current, mediated by α-adrenoceptors and this mechanism may play an important role in the α-adrenoceptor-mediated positive inotropic effect.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 325 (1984), S. 47-53 
    ISSN: 1432-1912
    Keywords: α-Adrenoceptors ; Phenylephrine ; Action potential ; Rabbit atrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Effects of α-adrenoceptor stimulation by phenylephrine (10−7–10−4 mol/l) in the presence of pindolol (10−7 mol/l) on the action potential and force of contraction were observed in the rabbit left atrium. 1. Phenylephrine reduced resting potential, prolonged action potential duration (APD), decreased maximum rate of rise of action potential ( $$\dot V_{{\text{max}}}$$ ) and increased force of contraction in a concentration-dependent manner. 2. Effects of phenylephrine (10−5 mol/l) were antagonized by prazosin (10−7 mol/l) or phentolamine (10−6 mol/l). 3. APD which had been prolonged by phenylephrine (10−5 mol/l) was slightly shortened by Ni2+ (0.3 mmol/l) at the level of 50% repolarization but almost unaffected at the level of 90% repolarization. TTX (10−6 mol/l) had no effect on ADP which had been prolonged by phenylephrine (10−5 mol/l). 4. Cs+ (10 mmol/l), which inhibits outward current i k 1, depolarized resting potential, but in contrast with phenylephrine Cs+ did not affect APD at 90% repolarization. 5. Phenylephrine (10−5 or 3×10−5 mol/l) restored Ca2+-dependent action potential and force of contraction in 20 mmol/l K+-Tyrode solution. These responses were suppressed by prazosin (10−7 mol/l) or Ni2+ (0.3 mmol/l). 6. Phenylephrine (10−5 or 10−4 mol/l) had no effect on steady-state membrane potential — $$\dot V_{{\text{max}}}$$ relationship. It is concluded that in the rabbit left atrium phenylephrine, via α-adrenoceptors may suppress outward currents perhaps i k 1 and i x, and might increase slow inward current.
    Type of Medium: Electronic Resource
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