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        <identifier>oai:www.ideals.illinois.edu:2142/72406</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_14828</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Sleator, William,</dc:contributor>
          <dc:creator>Burton, John Todd</dc:creator>
          <dc:date>2014-12-17T22:22:50Z</dc:date>
          <dc:date>2014-12-17T22:22:50Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1993</dc:date>
          <dc:date>1993</dc:date>
          <dc:description>Guinea pig left atria were suspended in a tissue bath of normal Krebs-Henseleit solution which was aerated with 95% O$\sb2$/5% CO$\sb2$ and maintained at 27$\sp\circ$C. The atria were attached to a force transducer and impaled with calcium sensitive micro-electrodes. The tissue was stimulated through 2 AgCl electrodes at 2 pulses per second (pps). When the tissue had reached a steady-state of contraction strength, rest intervals of 1 minute were introduced and the changes in the paracellular calcium levels were measured with the calcium sensitive micro-electrodes. The control condition produced an average increase during the interval in paracellular calcium concentration of 23.6 + 1.33 uM. Following treatment of the tissue with 8uM $3\sp\prime, 4\sp\prime$-di-chlorobenzamil (DCB), the average increase in paracellular calcium was 9.02 + 1.25 uM. DCB reduces the normal calcium efflux by 61.6 + 7.3%, n = 4, p $&amp;lt;$ 0.005. (Statistical analysis used paired one tail T-test.) 10 nM Ryanodine treated-tissue showed an increased efflux of calcium as measured by increased para-cellular calcium concentration of 9.8 + 1.9 uM over the control condition. 8uM DCB decreased the ryanodine treated tissues calcium efflux by 53.6 + 8.0%, n = 6, p $&amp;lt;$ 0.005, as measured by a decrease in the paracellular calcium concentration of 10.4 + 1.8 uM compared to the ryanodine treated condition. The cellular calcium efflux may be calculated from the measured changes in paracellular calcium concentration assuming an extracellular space of 47.8 ml/100 gm tissue. 8 uM DCB decreased the calcium efflux by 11.6 nmoles/sec per 100 gm tissue in non-ryanodine treated atria, and by 8.3 nmoles/sec per 100 gm of tissue in ryanodine treated atria. We conclude that DCB is an inhibitor of sodium-calcium exchange in guinea pig atria and that a measurable increase in paracellular calcium occurs during rest due to efflux of calcium from the cells via sodium-calcium exchange. In addition, we have shown that DCB decreases post-rest beat potentiation and this may indicate that sodium-calcium exchange plays a role in post-rest beat potentiation as well as the excitation-contraction coupling process.</dc:description>
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  Previous issue date: 1993</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 72574
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>86 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1993.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/72406</dc:identifier>
          <dc:identifier>(UMI)AAI9328985</dc:identifier>
          <dc:subject>Biology, Cell</dc:subject>
          <dc:subject>Biology, Animal Physiology</dc:subject>
          <dc:subject>Biophysics, Medical</dc:subject>
          <dc:title>Cellular Calcium Movements and Excitation-Contraction Coupling in Guinea Pig Atria</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Center for Biophysics and Computational Biology</department>
            <discipline>Biophysics</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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