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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 (JNV). Luminal distension following elevation of hydrostatic pressure to 18 cm H2O reversibly increased Jnv. Under control conditions Jnv and Na+-transport rates (JnNa) of colon were 2--3 times higher than those of rectum. In colon transepithelial electrical potential difference (psims) was time independent --12 mV (lumen negative) whereas rectal psims increased with time from --6 mV, reaching a plateau of --67 mV within 6 h. Amiloride 10(-4) mol.l-1 had no effect on psims, Jnv, and JnNa in colon but did slightly depress K+-secretion in colon descendens. In contrast, psims in rectum was dose-dependently depressed, being reversed to +7 mV at 10(-4) mol.l-1. Jnv and JnNa were decreased by half. Acetazolamide in addition to amiloride lowered the positive post-amiloride rectal psims by half. Adrenalectomy had no effect on colonic psims, but abolished psims of the rectum. A single dose of 40 microgram.kg-1 b.w. aldosterone during the experiment restored the typical time course of rectal psims, but did not affect psims 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.
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 (JNV). Luminal distension following elevation of hydrostatic pressure to 18 cm H2O reversibly increased Jnv. Under control conditions Jnv and Na+-transport rates (JnNa) of colon were 2--3 times higher than those of rectum. In colon transepithelial electrical potential difference (psims) was time independent --12 mV (lumen negative) whereas rectal psims increased with time from --6 mV, reaching a plateau of --67 mV within 6 h. Amiloride 10(-4) mol.l-1 had no effect on psims, Jnv, and JnNa in colon but did slightly depress K+-secretion in colon descendens. In contrast, psims in rectum was dose-dependently depressed, being reversed to +7 mV at 10(-4) mol.l-1. Jnv and JnNa were decreased by half. Acetazolamide in addition to amiloride lowered the positive post-amiloride rectal psims by half. Adrenalectomy had no effect on colonic psims, but abolished psims of the rectum. A single dose of 40 microgram.kg-1 b.w. aldosterone during the experiment restored the typical time course of rectal psims, but did not affect psims 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.
The kinetics of the electrogenic transfer of valine across rat jejunum was studied in vitro with an electrical technique. The operational kinetic parameters of ‘apparent K m ’ and the p. d. max (maximum transfer potential difference generated) were calculated and used to characterize the effects of diet and thyroid status on the electrogenic valine transfer mechanism. Hypothyroidism induced by 6-propyl-2-thiouracil (PTU), potassium thiocyanate, surgery or diet significantly increased the p. d. max but not the ‘apparent K m ’. Triiodothyronine (T 3 ) treatment reduced the elevated p. d. max in both the PTU-treated and thyroidectomized rats but thyroxine (T 4 ) was ineffective in the PTU group. The p. d. max and ‘apparent K m ’ in euthyroid rats were decreased by T 3 and T 4 but were unaltered by a 3-day fast. Fasting hypothyroid rats, however, did prevent the enhancement of p. d. max observed in hypothyroidism. Significant differences were observed in the p. d. max , the percentage 131 I protein bound in the serum and percentage 131 I uptake by the thyroid in rats fed notionally similar diets manufactured by two different suppliers but no differences were observed in total body O 2 uptake. The results obtained on giving supplemental iodine indicated that one of the diets altered thyroid function which significantly affected electrogenic valine transfer but not total body oxygen uptake. Thus electrogenic valine transfer is a more sensitive index of change in thyroid status than its conventional measure by total body oxygen uptake.
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