Literature DB >> 1693397

Effect of Na+ and K+ on Cl- distribution in guinea-pig vas deferens smooth muscle: evidence for Na+, K+, Cl- co-transport.

C C Aickin1, A F Brading.   

Abstract

1. Smooth muscle cells of the guinea-pig vas deferens after Cl- depletion actively reaccumulate ions to a level many times higher than that predicted by a passive distribution, even when anion exchange (largely responsible for Cl- movements in this preparation) is inhibited by DIDS (4,4'-diisothiocyanostilbene-2,2'-disulphonic acid). The cells therefore must possess a second mechanism for Cl- accumulation. We have now investigated the ionic requirement of this mechanism using a combination of ion analysis, 36Cl fluxes and direct measurement of the intracellular Cl- activity (aiCl). 2. In the steady state, the Cl- content of tissues was 12-16% less in Na(+)-free solution than in normal Krebs solution. 3. Loss of 36Cl into Cl(-)-free solution was slowed by the absence of Na+ and accelerated on its readdition. Uptake of 36Cl by Cl(-)-depleted tissues was also reduced in the absence of extracellular Na+, particularly at longer time intervals as uptake reached completion. These effects occurred in the presence and absence of CO2-HCO3- and in the presence of DIDS. 4. The initial rate of rise of aiCl on readdition of Cl- to Cl(-)-depleted cells was not significantly affected by the absence of Na+ in the presence of a functional anion exchange, but aiCl stabilized at a lower value than in normal solution. Readdition of Na+ stimulated a rise in aiCl to the control level. Removal and readdition of K+ under these conditions had negligible effects. 5. When anion exchange was inhibited by the presence of DIDS, removal and readdition of Na+ caused, respectively, a marked inhibition and stimulation of the rise in aiCl during Cl- reaccumulation. Under these conditions removal and readdition of K+ had similar effects. 6. The results suggest that Na+, K+, Cl- co-transport is involved in transmembrane movements of Cl- at least when the anion exchange mechanism is blocked. 7. The possibility that the marked effects of changes in external Na+ on transmembrane Cl- movements in the presence of a functional anion exchange mechanism are caused by secondary effects due to changes in intracellular pH as well as to suppression of Na+, K+, Cl- co-transport is discussed.

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Year:  1990        PMID: 1693397      PMCID: PMC1190071          DOI: 10.1113/jphysiol.1990.sp017931

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


  39 in total

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Journal:  J Physiol       Date:  1971-04       Impact factor: 5.182

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Authors:  T Ozawa; Y Saito; A Nishiyama
Journal:  Pflugers Arch       Date:  1988-10       Impact factor: 3.657

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Authors:  V A Kreye; P K Bauer; I Villhauer
Journal:  Eur J Pharmacol       Date:  1981-07-17       Impact factor: 4.432

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Authors:  R Casteels
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

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Journal:  TIT J Life Sci       Date:  1979

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Authors:  J S Wiley; R A Cooper
Journal:  J Clin Invest       Date:  1974-03       Impact factor: 14.808

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Authors:  R D Vaughan-Jones
Journal:  J Physiol       Date:  1979-10       Impact factor: 5.182

10.  Intracellular pH regulation in resting and contracting segments of rat mesenteric resistance vessels.

Authors:  C Aalkjaer; E J Cragoe
Journal:  J Physiol       Date:  1988-08       Impact factor: 5.182

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  5 in total

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4.  Mechanisms of intracellular Mg2+ regulation affected by amiloride and ouabain in the guinea-pig taenia caeci.

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5.  Regulation of intracellular pH in the smooth muscle of guinea-pig ureter: Na+ dependence.

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