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We are analyzing https://link.springer.com/article/10.1007/s004240000471.

Title:
Large-conductance calcium-activated potassium channels in neonatal rat intracardiac ganglion neurons | Pflügers Archiv - European Journal of Physiology
Description:
The properties of single Ca2+-activated K+ (BK) channels in neonatal rat intracardiac neurons were investigated using the patch-clamp recording technique. In symmetrical 140 mM K+, the single-channel slope conductance was linear in the voltage range –60/+60 mV, and was 207±19 pS. Na+ ions were not measurably permeant through the open channel. Channel activity increased with the cytoplasmic free Ca2+ concentration ([Ca2+]i) with a Hill plot giving a half-saturating [Ca2+] (K 0.5) of 1.35 µM and slope of ≅3. The BK channel was inhibited reversibly by external tetraethylammonium (TEA) ions, charybdotoxin, and quinine and was resistant to block by 4-aminopyridine and apamin. Ionomycin (1–10 µM) increased BK channel activity in the cell-attached recording configuration. The resting activity was consistent with a [Ca2+]i <100 nM and the increased channel activity evoked by ionomycin was consistent with a rise in [Ca2+]i to ≥0.3 µM. TEA (0.2–1 mM) increased the action potential duration ≅1.5-fold and reduced the amplitude and duration of the afterhyperpolarization (AHP) by 26%. Charybdotoxin (100 nM) did not significantly alter the action potential duration or AHP amplitude but reduced the AHP duration by ≅40%. Taken together, these data indicate that BK channel activation contributes to the action potential and AHP duration in rat intracardiac neurons.
Website Age:
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Keywords {🔍}

article, channels, channel, privacy, cookies, content, rat, neurons, duration, access, data, information, publish, search, potassium, intracardiac, activity, increased, action, potential, ahp, log, journal, research, pflügers, calciumactivated, neonatal, franciolini, hogg, catacuzzeno, ions, open, cai, charybdotoxin, discover, ion, springer, optional, personal, parties, policy, find, track, archiv, largeconductance, ganglion, published, november, cite, petris,

Topics {✒️}

month download article/chapter single-channel slope conductance rat intracardiac neurons patch-clamp recording technique cell-attached recording configuration single ca2+-activated related subjects full article pdf open channel action potential duration privacy choices/manage cookies channel activity increased action potential check access instant access channels european economic area scope submit manuscript voltage range –60/+60 mv hill plot giving external tetraethylammonium conditions privacy policy half-saturating [ca2+] accepting optional cookies article log apamin universita' di perugia main content log article cite article franciolini journal finder publish bk channel na+ ions afterhyperpolarization privacy policy books a personal data resting activity optional cookies manage preferences ions charybdotoxin essential cookies cookies skip subscription content similar content information institution subscribe journal publish data protection

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WebPage:
      mainEntity:
         headline:Large-conductance calcium-activated potassium channels in neonatal rat intracardiac ganglion neurons
         description: The properties of single Ca2+-activated K+ (BK) channels in neonatal rat intracardiac neurons were investigated using the patch-clamp recording technique. In symmetrical 140 mM K+, the single-channel slope conductance was linear in the voltage range –60/+60 mV, and was 207±19 pS. Na+ ions were not measurably permeant through the open channel. Channel activity increased with the cytoplasmic free Ca2+ concentration ([Ca2+]i) with a Hill plot giving a half-saturating [Ca2+] (K 0.5) of 1.35 µM and slope of ≅3. The BK channel was inhibited reversibly by external tetraethylammonium (TEA) ions, charybdotoxin, and quinine and was resistant to block by 4-aminopyridine and apamin. Ionomycin (1–10 µM) increased BK channel activity in the cell-attached recording configuration. The resting activity was consistent with a [Ca2+]i <100 nM and the increased channel activity evoked by ionomycin was consistent with a rise in [Ca2+]i to ≥0.3 µM. TEA (0.2–1 mM) increased the action potential duration ≅1.5-fold and reduced the amplitude and duration of the afterhyperpolarization (AHP) by 26%. Charybdotoxin (100 nM) did not significantly alter the action potential duration or AHP amplitude but reduced the AHP duration by ≅40%. Taken together, these data indicate that BK channel activation contributes to the action potential and AHP duration in rat intracardiac neurons.
         datePublished:2000-11-28T00:00:00Z
         dateModified:2000-11-28T00:00:00Z
         pageStart:629
         pageEnd:638
         sameAs:https://doi.org/10.1007/s004240000471
         keywords:
            Action potential Afterhyperpolarization Charybdotoxin Intracellular calcium Parasympathetic neurons Tetraethylammonium ions
            Human Physiology
            Molecular Medicine
            Neurosciences
            Cell Biology
            Receptors
         image:
         isPartOf:
            name:Pflügers Archiv
            issn:
               1432-2013
               0031-6768
            volumeNumber:441
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Springer-Verlag
            logo:
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               type:ImageObject
            type:Organization
         author:
               name:F. Franciolini
               affiliation:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                     address:
                        name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                        type:PostalAddress
                     type:Organization
               type:Person
               name:R. Hogg
               affiliation:
                     name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
                     address:
                        name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
                        type:PostalAddress
                     type:Organization
               type:Person
               name:L. Catacuzzeno
               affiliation:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                     address:
                        name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                        type:PostalAddress
                     type:Organization
               type:Person
               name:A. Petris
               affiliation:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                     address:
                        name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                        type:PostalAddress
                     type:Organization
               type:Person
               name:C. Trequattrini
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                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                     address:
                        name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                        type:PostalAddress
                     type:Organization
               type:Person
               name:D.J. Adams
               affiliation:
                     name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
                     address:
                        name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
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      headline:Large-conductance calcium-activated potassium channels in neonatal rat intracardiac ganglion neurons
      description: The properties of single Ca2+-activated K+ (BK) channels in neonatal rat intracardiac neurons were investigated using the patch-clamp recording technique. In symmetrical 140 mM K+, the single-channel slope conductance was linear in the voltage range –60/+60 mV, and was 207±19 pS. Na+ ions were not measurably permeant through the open channel. Channel activity increased with the cytoplasmic free Ca2+ concentration ([Ca2+]i) with a Hill plot giving a half-saturating [Ca2+] (K 0.5) of 1.35 µM and slope of ≅3. The BK channel was inhibited reversibly by external tetraethylammonium (TEA) ions, charybdotoxin, and quinine and was resistant to block by 4-aminopyridine and apamin. Ionomycin (1–10 µM) increased BK channel activity in the cell-attached recording configuration. The resting activity was consistent with a [Ca2+]i <100 nM and the increased channel activity evoked by ionomycin was consistent with a rise in [Ca2+]i to ≥0.3 µM. TEA (0.2–1 mM) increased the action potential duration ≅1.5-fold and reduced the amplitude and duration of the afterhyperpolarization (AHP) by 26%. Charybdotoxin (100 nM) did not significantly alter the action potential duration or AHP amplitude but reduced the AHP duration by ≅40%. Taken together, these data indicate that BK channel activation contributes to the action potential and AHP duration in rat intracardiac neurons.
      datePublished:2000-11-28T00:00:00Z
      dateModified:2000-11-28T00:00:00Z
      pageStart:629
      pageEnd:638
      sameAs:https://doi.org/10.1007/s004240000471
      keywords:
         Action potential Afterhyperpolarization Charybdotoxin Intracellular calcium Parasympathetic neurons Tetraethylammonium ions
         Human Physiology
         Molecular Medicine
         Neurosciences
         Cell Biology
         Receptors
      image:
      isPartOf:
         name:Pflügers Archiv
         issn:
            1432-2013
            0031-6768
         volumeNumber:441
         type:
            Periodical
            PublicationVolume
      publisher:
         name:Springer-Verlag
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:F. Franciolini
            affiliation:
                  name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                  address:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:R. Hogg
            affiliation:
                  name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
                  address:
                     name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
                     type:PostalAddress
                  type:Organization
            type:Person
            name:L. Catacuzzeno
            affiliation:
                  name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                  address:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:A. Petris
            affiliation:
                  name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                  address:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:C. Trequattrini
            affiliation:
                  name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
                  address:
                     name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
                     type:PostalAddress
                  type:Organization
            type:Person
            name:D.J. Adams
            affiliation:
                  name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
                  address:
                     name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
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      name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
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         name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
         type:PostalAddress
      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
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         name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
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      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
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         name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
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         name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
         type:PostalAddress
      name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
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            name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
            address:
               name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
               type:PostalAddress
            type:Organization
      name:R. Hogg
      affiliation:
            name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
            address:
               name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
               type:PostalAddress
            type:Organization
      name:L. Catacuzzeno
      affiliation:
            name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
            address:
               name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
               type:PostalAddress
            type:Organization
      name:A. Petris
      affiliation:
            name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
            address:
               name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
               type:PostalAddress
            type:Organization
      name:C. Trequattrini
      affiliation:
            name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia
            address:
               name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
               type:PostalAddress
            type:Organization
      name:D.J. Adams
      affiliation:
            name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072
            address:
               name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
      name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
      name:Dipartmento Biologia Cellulare e Molecolare, Universita' di Perugia, Via Pascoli 1, 06100 Perugia, Italy
      name:Department of Physiology and Pharmacology, University of Queensland, Brisbane, QLD 4072, Australia
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