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   <subfield code="a">Aldosterone regulates paracellular pathway resistance in rabbit distal colon</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Bernhard Hoffmann, Isolde Nagel, Wolfgang Clauss]</subfield>
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   <subfield code="a">Summary: Regulation of the paracellular pathway in rabbit distal colon by the hormone aldosterone was investigated in vitro in Ussing chambers by means of transepithelial and microelectrode techniques. To evaluate the cellular and paracellular resistances an equivalent circuit analysis was used. For the analysis the apical membrane resistance was altered using the antibiotic nystatin. Under control conditions two groups of epithelia were found, each clearly dependent on the light: dark regime. Low-transporting epithelia (LT) were observed in the morning and high-transporting epithelia (HT) in the afternoon. Na+ transport was about 3-fold higher in HT than in LT epithelia. Incubating epithelia of both groups with 0.1 μmol·1-1 aldosterone on the serosal side nearly doubled in LT epithelia the short circuit current and transepithelial voltage but the transepithelial resistance was not influenced. Maximal values were reached after 4-5 h of aldosterone treatment. In HT epithelia due to the effect of aldosterone all three transepithelial parameters remained constant over time. Evaluation of the paracellular resistance revealed a significant increase after aldosterone stimulation in both epithelial groups. This increase suggests that tight junctions might have been regulated by aldosterone. The hormonal effect on electrolyte transport was also dependent on the physiological state of the rabbit colon. Since net Na+ absorption in distal colon is, in addition to transcellular absorption capacity, also dependent on the permeability of the paracellular pathway, the regulation of tight junctions by aldosterone may be a potent mechanism for improving Na+ absorption during hormone-stimulated ion transport.</subfield>
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   <subfield code="a">Springer-Verlag, 1990</subfield>
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   <subfield code="a">Rabbit</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Distal colon</subfield>
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   <subfield code="a">Aldosterone</subfield>
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   <subfield code="a">Socium absoption</subfield>
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   <subfield code="a">Nystatin</subfield>
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   <subfield code="a">V t : transepithelial potential difference (mV)</subfield>
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   <subfield code="a">R t : transepithelial resistance (Ω·cm2)</subfield>
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   <subfield code="a">G t : transepithelial conductance (mS·cm-2)</subfield>
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   <subfield code="a">Isc : calculated short circuit current (μA·cm-2)</subfield>
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   <subfield code="a">V a : apical membrane potential difference (mV)</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">V bl : basolateral membrane potential difference (mV)</subfield>
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   <subfield code="a">α : voltage divider ratio</subfield>
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   <subfield code="a">R a : apical membrane resistance (Ω·cm2)</subfield>
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   <subfield code="a">R bl : basolateral membrane resistance (Ω·cm2)</subfield>
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   <subfield code="a">R c : cellular resistance (Σ of apical and basolateral resistance) (Ω·cm2)</subfield>
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   <subfield code="a">R p : resistance of the paracellular pathway (Ω·cm2)</subfield>
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   <subfield code="a">G a : apical membrane conductance (mS·cm-2)</subfield>
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   <subfield code="a">G bl : basolateral membrane conductance (mS·cm-2)</subfield>
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   <subfield code="a">G p : paracellular conductance (mS·cm-2)</subfield>
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   <subfield code="a">G t : transepithelial conductance (mS·cm-2)</subfield>
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   <subfield code="a">HT contr : high transporting control epithelia</subfield>
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   <subfield code="a">HT aldo : aldosterone incubated high transporting epithelia</subfield>
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   <subfield code="a">LT aldo : aldosterone incubated low transporting epithelia</subfield>
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