Literature DB >> 4825475

The sodium-transporting compartment of the epithelium of frog skin.

M Cereijido, C A Rabito, E Rodríguez Boulan, C A Rotunno.   

Abstract

1. The abdominal frog skin was mounted between two chambers containing Ringer with 1 mM-Na on the outside and 115 mM-Na on the inside. When the Na concentration of the outer solution ([Na](o)) is instantaneously raised from 1 to 50 mM, the short circuit current (I) increases to a new value in less than a second, and becomes essentially time-independent. Only in a few experiments was it observed to increase further, although at a much slower rate.2. At a time t after this increase, the addition of 10(-4)M amiloride to the outer solution produces an exponential decrease of I. The area under this exponential curve is generally taken to reflect the existence of a Na- transporting compartment (NaTC).3. The amount of Na represented by NaTC is a function of t: it increases from 1.7 x 10(-9) mole. cm(-2), at t = 10 sec, to 22.8 x 10(-9) mole. cm(-2) at t = 10 min.4. In view of the fact that (a) I is not a function of the size of the ;NaTC' and (b) that whereas I reaches a steady value in a fraction of a second the size of NaTC keeps increasing for minutes, it is proposed that the ;NaTC' represents an amount of Na which is not located along the main route of transepithelial transport.5. On the assumption that the NaTC is located in a cellular compartment and that, in order to accumulate in this compartment Na should be accompanied by a permeable anion, a series of experiments were performed with Ringer in which Cl(-) was replaced by gluconate. It was observed as expected, that NaTC in gluconate is 164 times smaller than in Cl(-), but I only decreases to one half its value in Cl(-) Ringer.

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Year:  1974        PMID: 4825475      PMCID: PMC1350905          DOI: 10.1113/jphysiol.1974.sp010498

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  33 in total

1.  Fluxes and distribution of sodium in frog skin. A new model.

Authors:  M Cereijido; C A Rotunno
Journal:  J Gen Physiol       Date:  1968-05       Impact factor: 4.086

2.  Anionic dependence of sodium transport in the frog skin.

Authors:  K T Ferreira
Journal:  Biochim Biophys Acta       Date:  1968-06-11

3.  Compartmentation of the sodium transport pool of the toad bladder.

Authors:  J C Vanatta; L A Bryant
Journal:  Proc Soc Exp Biol Med       Date:  1970-02

4.  Effect of Amiloride on sodium transport of frog skin. I. Action on intracellular sodium content.

Authors:  W Nagel; A Dörge
Journal:  Pflugers Arch       Date:  1970       Impact factor: 3.657

5.  Quantitative relation between hydrostatic pressure gradient, extracellular volume and active sodium transport in the epithelium of the frog skin (R. temporaria).

Authors:  C L Voute; H H Ussing
Journal:  Exp Cell Res       Date:  1970-10       Impact factor: 3.905

6.  Unstirred layers in frog skin.

Authors:  J Dainty; C R House
Journal:  J Physiol       Date:  1966-01       Impact factor: 5.182

7.  Location of the mechanism of active transport of sodium across the frog skin.

Authors:  C A Routunno; M I Pouchan; M Cereijido
Journal:  Nature       Date:  1966-05-07       Impact factor: 49.962

8.  Nonsteady-state three compartment tracer kinetics. II. Sodium flux transients in the toad urinary bladder in response to short circuit.

Authors:  T L Schwartz; F M Snell
Journal:  Biophys J       Date:  1968-07       Impact factor: 4.033

9.  Effect of amiloride on sodium transport in frog skin. II. Sodium transport pool and unidirectional fluxes.

Authors:  A Dörge; W Nagel
Journal:  Pflugers Arch       Date:  1970       Impact factor: 3.657

10.  Na transport across frog skin at low external Na concentrations.

Authors:  T U Biber; R A Chez; P F Curran
Journal:  J Gen Physiol       Date:  1966-07       Impact factor: 4.086

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  10 in total

1.  Chloride dependence of active sodium transport in frog skin: the role of intercellular spaces.

Authors:  K T Ferreira; B S Hill
Journal:  J Physiol       Date:  1978-10       Impact factor: 5.182

2.  Transepithelial potential difference in the proximal tubule of necturus kidney.

Authors:  A Edelman; T Anagnostopoulos
Journal:  Pflugers Arch       Date:  1976-05-12       Impact factor: 3.657

3.  The passive permeability of the skin of anuran amphibia: a comparison of frogs (Rana pipiens) and toads (Bufo marinus).

Authors:  P J Bentley; T Yorio
Journal:  J Physiol       Date:  1976-10       Impact factor: 5.182

4.  Interaction between cell sodium and the amiloride-sensitive sodium entry step in rabbit colon.

Authors:  K Turnheim; R A Frizzell; S G Schultz
Journal:  J Membr Biol       Date:  1978-03-10       Impact factor: 1.843

5.  Saturable K+ pathway across the outer border of frog skin (rana temporaria): kinetics and inhibition by Cs+ and other cations.

Authors:  W Zeiske; W Van Driessche
Journal:  J Membr Biol       Date:  1979-05-07       Impact factor: 1.843

6.  The sodium transport pool in toad urinary bladder epithelial cells.

Authors:  A D Macknight; M M Civan; A Leaf
Journal:  J Membr Biol       Date:  1975       Impact factor: 1.843

7.  Transients in toad skin: short circuit current and ionic fluxes related to inner sodium substitution by monovalent cations.

Authors:  W A Varanda; F L Vieira
Journal:  J Membr Biol       Date:  1978-03-20       Impact factor: 1.843

8.  Control of sodium permeability of the outer barrier in toad skin.

Authors:  L H Bevevino; F Lacaz-Vieira
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

9.  Amiloride and calcium effect on the outer barrier of the frog skin.

Authors:  C A Rabito; C A Rotunno; M Cereijido
Journal:  J Membr Biol       Date:  1978-09-18       Impact factor: 1.843

10.  Polarized monolayers formed by epithelial cells on a permeable and translucent support.

Authors:  M Cereijido; E S Robbins; W J Dolan; C A Rotunno; D D Sabatini
Journal:  J Cell Biol       Date:  1978-06       Impact factor: 10.539

  10 in total

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