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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 267 (1990), S. 301-304 
    ISSN: 0014-5793
    Keywords: Acetylcholine ; Aluminium ; Ca^2^+-activated Cl^- current ; Caffeine
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0014-5793
    Keywords: Acetylcholine ; Ca^2^+ inhibition of Ca^2^+ release ; Ca^2^+-induced Ca^2^+ release ; Cl^- current ; Inositol trisphosphate
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1424
    Keywords: cholecytokinin ; Ca2+ signal ; caffeine ; heparin ; G protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The effects on the cytosolic Ca2+ concentration of activating cholecystokinin receptors on single mouse pancreatic acinar cells have been investigated using patch-clamp whole-cell recording of Ca2+-dependent Cl− current. We used the nonsulphated octapeptide of cholecystokinin (CCK8-NS) since the effects of even high concentrations were rapidly reversible which was not the case for the sulphated octapeptide. A submaximal concentration of CCK8-NS (10nm) evoked a current response consisting of short-lasting (a few seconds) spikes, and some of these spikes were seen to trigger larger and longer (about half a minute) current pulses. At a higher concentration (100nm) CCK8-NS evoked smooth and sustained responses. The effect of CCK8-NS was almost abolished when the internal perfusion solution contained a high concentration of the Ca2+ chelator EGTA (5mm). The responses evoked by CCK8-NS were independent of the presence of Ca2+ in the external solution at least for the first 5 min of stimulation. Internal perfusion with GTP-γ-S markedly potentiated the effect of CCK8-NS or at a higher concentration itself induced responses very similar to those normally evoked by CCK8-NS. Caffeine added to the external solution at a low concentration (0.2–1mm) enhanced weak CCK8-NS responses, whereas high caffeine concentrations always inhibited the CCK8-NS-evoked responses. These inhibitory caffeine effects were quickly reversible. Forskolin evoked a similar inhibitory effect. Intracellular heparin (200 μg/ml) infusion markedly inhibited the response to CCK8-NS stimulation. We conclude that the primary effect of activating CCK receptors is to induced inositoltrisphosphate (IP3) production. IP3 evokes a small and steady Ca2+ release, and this in turn evokes pulsatile release of a larger magnitude from a caffeine-sensitive Ca2+ pool. The action of CCK is thus very similar to that previously established for muscarinic receptor activation in the same cells. Nevertheless, the pattern of the cytosolic Ca2+ fluctuations are different, and the basic process of Ca2+-induced Ca2+ release and Ca2+ signal spreading must therefore be modulated by a messenger yet unknown.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 386 (1980), S. 261-267 
    ISSN: 1432-2013
    Keywords: Salivary gland ; Acinar cells ; Membrane potential ; Membrane resistance ; ACh action ; ACh equilibrium potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The ionic dependence of the acetylcholine equilibrium potential (EACh) of acinar cells in which acetylcholine (ACh) induced hyperpolarization under control conditions was investigated using intracellular micro-electrode recording in superfused segments of mouse submaxillary gland. For measurements of EACh two micro-electrodes were inserted into neighbouring communicating cells, direct current was passed through one of these electrodes and EACh was determined by plotting the relation between the size of the ACh potential and the resting potential. ACh was applied by micro-iontophoresis. A complex potential change was induced by ACh when the membrane potential was set at high levels (−50∼ −80 mV). The appearance of complex responses dependend on the external [Na]. A severe reduction in external Na concentration abolished the appearance of complex responses, whereas alterations of external K concentration had no such effect. The results indicate that a depolarizing component separate from the hyperpolarizing component exists even in acinic in which ACh only evokes hyperpolarization under control conditions. Intracellular injection of TEA ions converted the ACh evoked potential change from hyperpolarization to depolarization in acini superfused with solutions containing Na in concentrations between 50 and 135 mM. However, the conversion was never obtained using solutions with low Na concentration (12.5 mM). The mean EACh was −60 mV under normal conditions. EACh was made more negative (5 mV) by a reduction in external Na concentration from 135 to 12.5 mmol·l−1. EACh was influenced by alterations of external K concentration, particularly when combined with reduction in external Na concentration. Alteration of K concentration from 2 to 20 mmol·l−1 shifted EACh to more positive values by about 40 mV. EACh in acini treated with TEA was about −28 mV in control solution (Na: 135 mmol·l−1) and −35 mV in a low Na concentration (50 mmol·l−1). Assuming that the response in submaxillary gland acinar cells to ACh under control condition is composed of two different kinds of potential changes (depolarization and hyperpolarization), the ionic basis of each of the potential changes and a possible explanation for the mechanism of ACh are discussed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 403 (1985), S. 109-111 
    ISSN: 1432-2013
    Keywords: guinea-pig vas deferens ; noradrenaline ; depolarization ; membrane conductance ; NA reversal potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The electrical response of the smooth muscle of guinea-pig vas deferens to exogenously applied noradrenaline (NA) was examined using the double sucrose-gap method. NA evoked a depolarization of the smooth muscle membrane which was associated with an increase in the size of electrotonic potentials. A conditioning depolarization of the membrane induced by current application enhanced the size of NA-induced depolarization, whereas a conditioning hyperpolarization reduced it. When a conditioning hyperpolarization of 25 mV in magnitude was applied, the direction of potential change induced by NA was reversed. These results are discussed with respect to the ionic mechanism of the electrical event in response to NA in this tissue.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2013
    Keywords: guinea-pig vas deferens ; adenosine triphosphate ; depolarization ; membrane conductance ; ATP reversal potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of exogenously applied adenosine triphosphate (ATP) on the smooth muscle of guinea-pig vas deferens were studied with the double sucrose-gap method. ATP evoked a membrane depolarization which was associated with a decrease in the size of electrotonic potentials. Conditioning hyperpolarization induced by current application caused an increase in the magnitude of the ATP-induced depolarization; the larger the conditioning hyperpolarization, the greater the ATP-induced depolarization. These results are discussed with respect to the ionic mechanism of the electrical event in response to ATP in this tissue.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 340 (1989), S. 272-272 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] PETERSEN ET AL. REPLY-Rink's attempt to resurrect the theory that pulsatile inositol (1,4,5) trisphosphate (InsP3) production is responsible for intracellular Ca2+ spikes involves a complicated explanation and an unlikely assumption. Our data1 show that inositol (1,4,5) trisphos-phorothioate ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2013
    Keywords: Key words Cyclic AMP ; Ca2+ channel ; Islet β-cells ; Patch-clamp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Intracellular cAMP-dependent modulation of L-type Ca2+ channel activation in cultured rat islet β-cells has been investigated using the patch-clamp whole-cell current recording mode. The L-type voltage-dependent Ca2+ current (I Ca) showed a fast activation followed by a slow inactivation, and was sensitive to Ca2+ channel blockers, for example nifedipine. Application of a cAMP analogue, dibutyryl cyclic AMP (db-cAMP), increased the magnitude of the peak I Ca in a concentration-dependent manner. Values of the half-activation potentials (V 1/2), taken from activation curves for I Ca, were –16.7 ± 1.8 and –21.9 ± 3.4 mV (P 〈 0.05) before and after application of db-cAMP, respectively, with no change of the slope factor (k) or the reversal potential. Pretreatment with a specific protein kinase A antagonist, Rp-cAMP, prevented the potentiating effect of db-cAMP. These results indicate that in rat islet β-cells, phosphorylation of cAMP-dependent kinase potentiates the voltage-dependent activation of L-type Ca2+ channels.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 386 (1980), S. 251-259 
    ISSN: 1432-2013
    Keywords: Salivary gland ; Acinar cell ; Membrane potential ; ACh action ; Atropine ; Tetraethylammonium ; D600
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The responses in membrane potential and resistance of acinar cells to iontophoretically applied acetylcholine (ACh) were investigated using intracellular micro-electrode recording in superfused segments of mouse submaxillary gland. For measurements of membrane resistance and acetylcholine equilibrium potential (EACh), two micro-electrodes were inserted into neighbouring communicating cells. Current could be injected through one of the electrodes. The pattern of membrane potential change induced by ACh depended on the resting potential. Simple hyperpolarizations were induced at low resting potentials, while biphasic potential changes (depolarization followed by hyperpolarization) or simple depolarizations were observed at relatively high resting potentials. A similar dependence of the ACh induced potential change on the resting potential was obtained in experiments in which the resting membrane potential was set at different levels by injecting direct current and stimulating the same cell with equal doses of ACh. The ACh equilibrium potential ranged widely between −45 and −75 mV. Under special conditions the conversion in response to ACh from a hyperpolarization to depolarization could be obtained without change in resting potential. Small doses of ACh evoked simple depolarization, while medium doses induced biphasic responses and large doses of ACh caused hyperpolarization. The effect of a low concentration of atropine on the response was an initial block of hyperpolarization followed by a secondary block of depolarization. Intracellular injection of TEA ions converted the ACh induced potential response from hyperpolarization to depolarization. Both the depolarizing and hyperpolarizing ACh responses were accompanied by a marked reduction in membrane resistance. The depolarization was abolished by a severe reduction in external Na concentration, while the hyperpolarization was sensitive to alterations in external K concentration. These results indicate that some of the complex responses in submaxillary gland acinar cells to ACh may be explained by the interaction between two different kinds of potential change (Na dependent depolarization and K dependent hyperpolarization).
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 166 (1996), S. 369-374 
    ISSN: 1432-136X
    Keywords: Short-chain fatty acids ; Exocrine pancreas ; Acinar cells ; Cytosolic calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In order to investigate the cellular mechanisms involved in amylase release in response to stimulation with short-chain fatty acids, changes in intracellular calcium concentration ([Ca2+]i), membrane current and amylase release were measured in pancreatic acinar cells of sheep. Both octanoate and acetylcholine raised [Ca2+]i in acinar cells in a concentration-dependent manner. The rise in [Ca2+]i in response to the stimulation with octanoate (10 mmol·l-1) was reduced in a medium without CaCl2, but was markedly enhanced by reintroduction of CaCl2 into the medium up to 2.56 mmol·l-1. Perfusion of the cells with a medium containing octanoate (5 mmol·l-1) or acetylcholine (0.5 μmol·l-1) immediately raised inward current across the cell membrane at a holding-membrane potential of-30 mV. The inward current became greater as the holding potential became more negative. The equilibrium potential was 1.8 mV and 3.9 mV for octanoate and acetylcholine, respectively, being consistent with that for Cl-. Although intracellular application of octanoate through a patch-clamp pipette also raised inward current after several minutes in some cells (4 out of 12), this possibility was significantly smaller than that for extracellular application. In other cells, even though the intracellular application of octanoate did not cause an increase in current, it always caused responses immediately after introduction of the fatty acid into the medium. Stimulation with fatty acid as well as acetylcholine raised amylase release in a concentration-dependent manner in cells dispersed from tissue segments with crude collagenase and trypsin inhibitor. Without trypsin inhibitor, crude collagenase significantly and selectively reduced the octanoate (10 mmol·l-1)-induced amylase release. Dispersion with crude collagenase and trypsin significantly reduced both responses induced by octanoate and acetylcholine (5.5 μmol·l-1). We conclude that fatty acids and acetylcholine increase [Ca2+]i, which consequently evokes a rise in transmembrane ion (Cl-) conductance and amylase release, and that trypsin-sensitive protein(s) in the cell membrane are involved in secretory processes activated by stimulation with fatty acids in ovine pancreatic acinar cells.
    Type of Medium: Electronic Resource
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