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Amiloride Sensitivity of the Transepithelial Electrical Potential and of Sodium and Potassium Transport in Rat Distal Colon in Vivo

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Journal J Physiol
Specialty Physiology
Date 1981 Jan 1
PMID 7277236
Citations 18
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Abstract

1. The effect of amiloride within the gut lumen on the transepithelial electrical potential difference (p.d.) and Na and K transport by the distal colon of adrenalectomized (dexamethasone-maintained), normal, aldosterone-infused and Na-depleted groups of rats was examined. 2. Amiloride had no effect in adrenalectomized rats; in normal rats, only the p.d. was significantly reduced. 3. In the group given a short (2 hr) aldosterone infusion, amiloride reduced the elevated p.d. and K secretion rate to normal levels. There was no change in apparent K permeability of the epithelium. 4. In the Na-depleted group, p.d. and Na absorption were virtually abolished by amiloride but although K secretion was reduced it still remained much above normal levels. Adrenalectomy prevented the effects of Na depletion. 5. P.d. change occurred rapidly when amiloride was added to the perfusate. Increasing the Na concentration in the perfusate reduced the sensitivity to amiloride. Apparent 'Km' values estimated from p.d. changes (luminal Na, 50 mM) were similar for aldosterone-infused (7.6 X 10(-6) M) and Na-depleted (5.4 X 10(-6) M) rats. 6. Aldosterone appears to be essential for the induction of amiloride-sensitive Na paths in the mucosal plasma membrane of rat colonic epithelial cells. Prolonged aldosterone stimulation, as in the Na-depleted rats, increases the amiloride-sensitive Na paths while largely suppressing the amiloride-insensitive Na paths; in addition, the K/Na clearance rate ratio of the epithelium is increased. AMiloride interacts only with one set of Na paths and does not interact directly with K paths.

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References
1.
Bastl C, Binder H, HAYSLETT J . Role of glucocorticoids and aldosterone in maintenance of colonic cation transport. Am J Physiol. 1980; 238(3):F181-6. DOI: 10.1152/ajprenal.1980.238.3.F181. View

2.
Edmonds C, Marriott J . The effect of aldosterone and adrenalectomy on the electrical potential difference of rat colon and on the transport of sodium, potassium, chloride and bicarbonate. J Endocrinol. 1967; 39(4):517-31. DOI: 10.1677/joe.0.0390517. View

3.
Feldman D, Funder J, Edelman I . Subcellular mechanisms in the action of adrenal steroids. Am J Med. 1972; 53(5):545-60. DOI: 10.1016/0002-9343(72)90152-0. View

4.
Bentley P . Amiloride: a potent inhibitor of sodium transport across the toad bladder. J Physiol. 1968; 195(2):317-30. PMC: 1351665. DOI: 10.1113/jphysiol.1968.sp008460. View

5.
USSING H . Some aspects of the application of tracers in permeability studies. Adv Enzymol Relat Subj Biochem. 1952; 13:21-65. DOI: 10.1002/9780470122587.ch2. View