Membrane pathways for water and solutes in the toad bladder: II. Reflection coefficients of the water and solute channels
- PMID: 226714
- DOI: 10.1007/BF01871122
Membrane pathways for water and solutes in the toad bladder: II. Reflection coefficients of the water and solute channels
Abstract
Urea and water transport across the toad bladder can be separately activated by low concentrations of vasopressin or 8 Br-cAMP. Employing this method of selective activation, we have determined the reflection coefficient (sigma) of urea and other small molecules under circumstances in which the bladder was transporting urea or water. An osmotic method for the determination of sigma was used, in which the ability of a given solute to retard water efflux from the bladder was compared to that of raffinose (sigma = 1.0) or water (sigma = 0). When urea transport was activated (low concentration of vasopressin), sigma for urea and other solutes was low, (sigma urea, 0.08--0.39; sigma acetamide, 0.55; sigma ethylene glycol, 0.60). When water transport was activated (0.1 mM 8 Br-cAMP) sigma urea approached 1.0 sigma urea also approached 1.0 at high vasopressin concentrations. In a separate series of studies, sigma urea was determined in the presence of 2 x 10(-5) M KMnO4 in the luminal bathing medium. Under these conditions, when urea transport is selectively blocked, sigma urea rose from a value of 0.12 to 0.89. Thus, permanganate appears to "close" the urea transport channel. These findings indicate that the luminal membrane channels for water and solutes differ significantly in their dimensions. The solute channels, limited in number, have relatively large radii. They carry a small fraction (approximately 10%) of total water flow. The water transport channels, on the other hand, have small radii, approximately the size of a water molecule, and exclude solutes as small as urea.
Similar articles
-
Membrane pathways for water and solutes in the toad bladder: I. Independent activation of water and urea transport.J Membr Biol. 1979 Sep;49(3):253-68. doi: 10.1007/BF01871121. J Membr Biol. 1979. PMID: 226713
-
Effect of phloretin on water and solute movement in the toad bladder.J Clin Invest. 1973 Jun;52(6):1435-42. doi: 10.1172/JCI107317. J Clin Invest. 1973. PMID: 4703229 Free PMC article.
-
Selective inhibition of osmotic water flow by general anesthetics to toad urinary bladder.J Clin Invest. 1976 Oct;58(4):980-8. doi: 10.1172/JCI108552. J Clin Invest. 1976. PMID: 184113 Free PMC article.
-
Mass transport across cell membranes: the effects of antidiuretic hormone on water and solute flows in epithelia.Annu Rev Physiol. 1976;38:451-500. doi: 10.1146/annurev.ph.38.030176.002315. Annu Rev Physiol. 1976. PMID: 176921 Review. No abstract available.
-
Water permeability of biological membranes. Lessons from antidiuretic hormone-responsive epithelia.Biochim Biophys Acta. 1982 May 12;650(4):267-80. doi: 10.1016/0304-4157(82)90019-3. Biochim Biophys Acta. 1982. PMID: 6178435 Review. No abstract available.
Cited by
-
Does water drag solutes through kidney proximal tubule?Pflugers Arch. 1983 Apr;397(1):35-41. doi: 10.1007/BF00585165. Pflugers Arch. 1983. PMID: 6408602
-
Inhibition of vasopressin-stimulated water flow in toad bladder by phorbol myristate acetate, dioctanoylglycerol, and RHC-80267. Evidence for modulation of action of vasopressin by protein kinase C.J Clin Invest. 1985 Sep;76(3):1071-8. doi: 10.1172/JCI112060. J Clin Invest. 1985. PMID: 2995443 Free PMC article.
-
Effects of glutaraldehyde fixation on renal tubular function. I. Preservation of vasopressin-stimulated water and urea pathways in rat papillary collecting duct.Pflugers Arch. 1987 May;408(5):479-83. doi: 10.1007/BF00585072. Pflugers Arch. 1987. PMID: 3110736
-
Role of the endogenous kallikrein-kinin system in modulating vasopressin-stimulated water flow and urea permeability in the toad urinary bladder.J Clin Invest. 1981 Jun;67(6):1792-6. doi: 10.1172/jci110219. J Clin Invest. 1981. PMID: 6165739 Free PMC article.