Literature DB >> 2596592

Voltage-activated cation transport in human erythrocytes.

J A Halperin1, C Brugnara, M T Tosteson, T Van Ha, D C Tosteson.   

Abstract

We report here the effects of membrane potential on the permeability of the human erythrocyte to Na, K, and Ca. Membrane potential was changed either by varying the K concentration gradient in the presence of valinomycin or by varying the concentration gradient of the permeant anion nitrate in the presence of 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. When the membrane potential was changed from inside negative (-10 mV) to inside positive (greater than 40 mV), influx, efflux, and net flux of Na and K increased. Marked net cation loss and cell shrinkage occurred in the absence of a chemical gradient for Na and K. This voltage-dependent increase in Na and K conductance is partially inhibited by 10 microM ruthenium red and persists when the membrane potential is returned to -10 mV after transient exposure to inside-positive potentials. A similar voltage-dependent behavior was found for Ca influx. The voltage-activated Ca influx is almost completely inhibited by 10 microM ruthenium red.

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Year:  1989        PMID: 2596592     DOI: 10.1152/ajpcell.1989.257.5.C986

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  18 in total

1.  The human red cell voltage-regulated cation channel. The interplay with the chloride conductance, the Ca(2+)-activated K(+) channel and the Ca(2+) pump.

Authors:  P Bennekou; B I Kristensen; P Christophersen
Journal:  J Membr Biol       Date:  2003-09-01       Impact factor: 1.843

2.  Strain-specific variations in cation content and transport in mouse erythrocytes.

Authors:  Alicia Rivera; Robert Y L Zee; Seth L Alper; Luanne L Peters; Carlo Brugnara
Journal:  Physiol Genomics       Date:  2013-03-12       Impact factor: 3.107

3.  Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation.

Authors:  M Inaba; A Yawata; I Koshino; K Sato; M Takeuchi; Y Takakuwa; S Manno; Y Yawata; A Kanzaki; J Sakai; A Ban; K Ono; Y Maede
Journal:  J Clin Invest       Date:  1996-04-15       Impact factor: 14.808

4.  Ca(2+)-activated K+ channels of human and rabbit erythrocytes display distinctive patterns of inhibition by venom peptide toxins.

Authors:  C Brugnara; C C Armsby; L De Franceschi; M Crest; M F Euclaire; S L Alper
Journal:  J Membr Biol       Date:  1995-09       Impact factor: 1.843

5.  Carrier-mediated residual K+ and Na+ transport of human red blood cells.

Authors:  K Denner; R Heinrich; I Bernhardt
Journal:  J Membr Biol       Date:  1993-03       Impact factor: 1.843

6.  Activation of a novel organic solute transporter in mammalian red blood cells.

Authors:  S J Culliford; I Bernhardt; J C Ellory
Journal:  J Physiol       Date:  1995-12-15       Impact factor: 5.182

7.  Inhibition of Ca(2+)-dependent K+ transport and cell dehydration in sickle erythrocytes by clotrimazole and other imidazole derivatives.

Authors:  C Brugnara; L de Franceschi; S L Alper
Journal:  J Clin Invest       Date:  1993-07       Impact factor: 14.808

8.  The protective effect of propofol on erythrocytes during cardiopulmonary bypass.

Authors:  Shihai Zhang; Shanglong Yao
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2004

9.  Magnesium transport in magnesium-loaded ferret red blood cells.

Authors:  P W Flatman; L M Smith
Journal:  Pflugers Arch       Date:  1996-10       Impact factor: 3.657

10.  Hypoxia activates a Ca2+-permeable cation conductance sensitive to carbon monoxide and to GsMTx-4 in human and mouse sickle erythrocytes.

Authors:  David H Vandorpe; Chang Xu; Boris E Shmukler; Leo E Otterbein; Marie Trudel; Frederick Sachs; Philip A Gottlieb; Carlo Brugnara; Seth L Alper
Journal:  PLoS One       Date:  2010-01-15       Impact factor: 3.240

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