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  • 1
    ISSN: 1432-2013
    Keywords: Large intestine ; Aldosterone ; Anaesthesia ; Amiloride ; Ion transport ; Osmolyte transport ; Water transport ; Luminal steady state concentrations ; Transepithelial voltage ; Segmental heterogeneity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Thiobutabarbital anaesthetized and abdominally operated control rats develop high endogenous plasma levels of both aldosterone and corticosterone during the course of a 12 h experiment. This effect was used as a model for examining ‘acute’ steroid action (i) on net ion and water fluxes and (ii) on zero flux luminal limiting concentrations in rat upper colon (proximal 50% of large intestine) and rectum (distal 40%). Experiments of both kinds consisted of 8 independent 90 min measuring periods. (i) In rectum net fluxes of Na, K, osmolytes (sum of all solutes) and water started at low levels around zero, began to rise about 2 h after plasma levels of aldosterone had increased, and reached plateau values around the 6th hour of anaesthesia. In upper colon, fluxes of Na, K, Cl, and osmolytes were high from the beginning and did not vary significantly with time. (ii) At zero flux conditions limiting concentrations of Na in the hormonally unstimulated phase of the experiment were 20±3 mM in upper colon and 22±3 mM in rectum. After maximal endogenous aldosterone liberation zero flux concentrations were 5.2 mM in upper colon and 2.2 mM in rectum, corresponding to luminal fluid to plasma ratios (LF/P) of 0.040 and 0.016, respectively. Amiloride reduced the maximal Na gradient in rectum to aLF/P of 0.3 but was not effective in upper colon and did not prevent the stimulating effect of aldosterone in this segment. Under all experimental conditions zero flow concentrations of K were higher than consistent with a solely passive distribution, indicating simultaneous passive and active secretion in both segments. In contrast to the findings of others, the luminal fluid remained isoosmolar with plasma in all zero flux experiments. Conclusions: Under acute elevation of steroid levels not higher than reached in a living animal the rectum varies net fluxes of Na, K, osmolytes, and water between zero and high rates. At this range of steroid levels, the upper colon practically does not respond with variations in net fluxes. Under zero flux conditions aldosterone acutely increases maximal Na gradients in rectum and, to a lesser degree, also in upper colon. Thus, acutely elevated aldosterone levels affect Na transport in upper colon and rectum by different mechanisms and intensities: in rectum, which is the most sensitive site of transport regulation, via an amiloridesensitive Na-pathway, and in upper colon, via an amiloride-insensitive pathway.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 378 (1978), S. 71-83 
    ISSN: 1432-2013
    Keywords: Intestinal perfusion parameters ; Adrenalectomy ; Aldosterone ; Amiloride ; Anesthesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Functionally isolated segments of rat colon and rectum were perfused in situ in a closed loop system. Rectum was defined as the lower 25–35% of the length of large intestine (cecum excluded). Perfusion conditions were optimized at 0.5 ml·min−1 and 3 cm H2O luminal pressure. Variation of perfusion rate between 0.2 and 2 ml·min−1 did not influence net volume transport (J v n ). Luminal distension following elevation of hydrostatic pressure to 18 cm H2O reversibly increasedJ v n . Under control conditionsJ v n and Na+-transport rates (J Na n ) of colon were 2–3 times higher than those of rectum. In colon transepithelial electrical potential difference ψms was time independent −12 mV (lumen negative) whereas rectal ψms increased with time from −6 mV, reaching a plateau of −67 mV within 6h. Amiloride 10−4 mol·l−1 had no effect on ψms,J v n , andJ Na n in colon but did slightly depress K+-secretion in colon descendens. In contrast, ψms in rectum was dosedependently depressed, being reversed to +7 mV at 10−4 mol·l−1.J v n andJ Na n were decreased by half. Acetazolamide in addition to amiloride lowered the positive post-amiloride rectal ψms by half. Adrenalectomy had no effect on colonic ψms, but abolished ψms of the rectum. A single dose of 40 μg·kg−1 b.w. aldosterone during the experiment restored the typical time course of rectal ψms, but did not affect ψms in colon. It is concluded that aldosterone induces an amiloride-sensitive Na+-pathway only in rectum, but not in colon, and that colon and rectum differ basically in their transport properties, quantitatively as well as qualitatively, as do the kidney distal convoluted tubule and the cortical collecting duct.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2013
    Keywords: Adrenalectomy ; Aldosterone ; K absorption ; K secretion ; Na transport ; Osmolyte transport ; Proximal colon ; Rectal colon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The short-term action of aldosterone in physiological concentration on net fluxes of Na, K, Cl, HCO3, osmolytes, and water was examined in the proximal colon and rectal colon of adrenalectomized (ADX) rats in vivo. The measuring time was 12 h, divided in eight periods of 90 min. (a) Aldosterone alone (6 nmol h−1kg−1) did not stimulate transport in ADX rats. In these experiments plasma [K] increased to fatal values. A basal glucocorticoid substitution of 24 nmol h−1kg−1 corticosterone caused plasma K to stay constant throughout the experiment, so that epithelial transport was not handicapped by non-specific effects of ADX, but this also did not restore the decreased transport of ADX rats to control values. Under these conditions (absence of aldosterone) in the rectal colon Na and H2O transport was zero, whereas in the proximal colon flux rates were depressed by between 30% and 50%. In contrast, basal glucocorticoid substitution of 18 nmol h−1kg−1 corticoster-one plus infusion of 6 nmol h−1kg−1 aldosterone caused transport stimulation to values not significantly different from those of non-ADX controls. We conclude that after ADX, aldosterone at physiological concentrations increases transport if, as a prerequisite, a basal glucocorticoid substitution is provided. Transport of Na, K, and H2O is under the total control of aldosterone in the rectal colon but is only moderately altered in the proximal colon. (b) In the proximal colon aldosterone is effective on electroneutral Na transport consistent with the Na/H, Cl/HCO3 double exchanger, while in the rectal colon aldosterone controls the amiloride-sensitive Na channel, which is the sole apical Na transporter in that segment. In this respect the rectal colon is functionally distinct from the distal colon of other studies in the rat, where under unstimulated conditions the double exchanger is present. Regarding Na transport mechanisms, the rat large intestine thus consists of three distinct segments, the proximal, distal, and rectal colon. (c) In the rectal, but not the proximal colon, active net K absorption against the electrochemical gradient took place in the absence of aldosterone, but was suppressed in its presence. (d) The flux ratio of osmolytes over H2O was constantly hypertonic as compared to the plasma (387±1 mosmol l−1), independent of absolute flux size, the colonic segment examined, or the steroid concentration used. This effect may be due to a hypertonic unstirred layer within the lamina propria.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2013
    Keywords: Colon ; Rectum ; Epithelial resistance ; AC impedance ; Stripping ; Subepithelial resistance ; Aldosterone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Epithelial and subepithelial electrical resistances of rat large intestine were measured by means of a 4-electrode AC impedance technique in three segments, colon ascendens, colon descendens and rectum. (i) Epithelial resistance of colon ascendens and colon descendens was about 35 Ω · cm2 and not different between these two segments. It was, however, about 3 times higher in rectum (99 Ω · cm2). This finding is in accord with our previous observation of about 3-fold higher net fluxes of ions and water in colon ascendens and colon descendens than in rectum. It confirms the concept of a main functional difference between the terminal part of the large intestine (rectum) and the more proximal segments (colon). (ii) The acutely (within hours) varied level of aldosterone by keeping the rats for 7 h in anaesthesia caused in the rectum a more than 10-fold increase in short circuit current (I SC) and transepithelial voltage but no significant decrease in resistance. Similarly, the decline inI SC, as regularly observed in the early phase of in vitro measurements on partially stripped large intestine, was paralleled by voltage changes but not by changes in resistance. We conclude that the wide range of resistance values published so far was caused to a great extent by including various portions of colon or rectum. (iii) By comparing intact (not stripped) and partially stripped preparations (muscularis propria removed) of the rectum it was shown that partial stripping did not alter the epithelial resistance but reduced the subepithelial resistance in this segment from 26 to 8 Ω · cm2, or by 68%. Subepithelial resistances of stripped rectum, colon ascendens and colon descendens were 8, 12 and 13 Ω · cm2, respectively. Based on these figures,I SC of conventional voltage clamp measurements is underestimated due to subepithelial tissue layers in intact rectum by 23% and in the partially stripped preparations of rectum, colon ascendens and colon descendens by 9%, 34%, and 37%, respectively.
    Type of Medium: Electronic Resource
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