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  • 1
    ISSN: 1432-2013
    Keywords: Ischaemia ; Reperfusion ; Chloride conductance ; Potassium conductance ; Action potential ; ATP ; Rat skeletal muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Electrical parameters of extensor digitorum longus (EDL) muscles and their contralaterals were measured “in vitro” at 30°C by a computerized two intracellular microelectrode technique after ischaemia and postischaemic reflow. In some muscles the adenosine triphosphate (ATP) levels are also measured. Ischaemia led to a 39% reduction of Cl− conductance (G Cl), whereas reperfusion increase G Cl by 18% with respect to contralateral control muscles. Ischaemia and reperfusion increased K+ conductance (G K) by 21% and 68%, respectively; this increased was reversed by 50 μM glybenclamide, suggesting an involvement of ATP-sensitive K+ channels. A statistically significant hyperpolarization and increase in excitability was observed after ischaemia, whereas after the reflow period the fibres were depolarized and less excitable. Ischaemia and reperfusion lowered the intracellular ATP content by 18% and 64%, respectively.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Frog ; Skeletal muscle ; Chloride conductance ; Potassium conductance ; Protein kinase C ; Protein kinase A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The membrane electrical properties and resting ionic conductances of frog semitendinosus muscle fibres were studied in vitro at 25° C with the two-microelectrode cable technique, in the presence of an activator or inhibitor of protein kinase C (PKC) or in the presence of an activator of adenylate cyclase. The PKC activator, 4β-phorbol 12,13-dibutyrate (4β-PDB), reduced chloride conductance (G Cl) at concentrations greater than 1 μM and did not affect potassium conductance (G K). At 150 μM, the maximum concentration of 4β-PDB tested, G Cl was reduced by 42%. The “inactive” phorbol ester 4α-phorbol 12,13-dibutyrate did not affect G Cl or G K. The inhibitory effect of 4β-PDB on G Cl was prevented by pretreatment of the muscle preparation with the PKC inhibitor staurosporine. The adenylate cyclase activator forskolin (1.5–8 μM) significantly increased the G K of the fibres, without affecting G Cl. Thus, we conclude that frog skeletal muscle G Cl, unlike rat muscle G Cl, is relatively insensitive to activators of PKC. Moreover, in frog muscle, protein kinase A is a likely modulator of G K, but not G Cl.
    Type of Medium: Electronic Resource
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