Literature DB >> 7085644

Permeability of canine cardiac sarcoplasmic reticulum vesicles to K+, Na+, H+, and Cl-.

G Meissner, D McKinley.   

Abstract

Cardiac muscle sarcoplasmic reticulum appears to contain channel-like structures that render the membrane permeable to small univalent ions. Canine heart microsomes fractionated according to buoyant density were examined by Millipore filtration, light scattering, and membrane potential m easurements. Enzymatic analysis and measurement of D-glucose permeation and Na/Ca exchange systems indicated two membrane fractions suitable for the permeability studies, one enriched in surface membranes with a buoyant density of 1.04-1.11 (10-25% sucrose) and one enriched in sarcoplasmic reticulum with a buoyant density of 1.13-1.15 (30-34% sucrose). Surface membrane vesicles impermeable to [3H]sucrose were largely impermeable to K+, Na+, and Cl-, while sarcoplasmic reticulum vesicles impermeable to [3H]sucrose were readily permeable to K+, Na+, H+, and Cl-. Sarcoplasmic reticulum vesicles were essentially impermeable to Ca2+, Mg2+, choline+, gluconate-, 1,4-piperazinediethanesulfonic acid (Pipes-), and D-glucose. These results suggest that cardiac muscle sarcoplasmic reticulum contains structures that facilitate the movement of small univalent ions. A possible function of these putative ion-conducting structures may be to allow rapid ion fluxes to counter electrogenic Ca2+ fluxes across sarcoplasmic reticulum during cardiac muscle contraction and relaxation.

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Year:  1982        PMID: 7085644

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  22 in total

Review 1.  Ion conduction and discrimination in the sarcoplasmic reticulum ryanodine receptor/calcium-release channel.

Authors:  A J Williams
Journal:  J Muscle Res Cell Motil       Date:  1992-02       Impact factor: 2.698

2.  Blockade of cardiac sarcoplasmic reticulum K+ channel by Ca2+: two-binding-site model of blockade.

Authors:  Q Y Liu; H C Strauss
Journal:  Biophys J       Date:  1991-07       Impact factor: 4.033

3.  Sarcoplasmic reticulum K(+) (TRIC) channel does not carry essential countercurrent during Ca(2+) release.

Authors:  Tao Guo; Alma Nani; Stephen Shonts; Matthew Perryman; Haiyan Chen; Thomas Shannon; Dirk Gillespie; Michael Fill
Journal:  Biophys J       Date:  2013-09-03       Impact factor: 4.033

4.  Monovalent cationic channel activity in the inner membrane of nuclei from skeletal muscle fibers.

Authors:  Viktor Yarotskyy; Robert T Dirksen
Journal:  Biophys J       Date:  2014-11-04       Impact factor: 4.033

5.  Solubilisation and reconstitution of the rabbit skeletal muscle sarcoplasmic reticulum K+ channel into liposomes suitable for patch clamp studies.

Authors:  B Tomlins; A J Williams
Journal:  Pflugers Arch       Date:  1986-09       Impact factor: 3.657

6.  Potassium channel of cardiac sarcoplasmic reticulum is a multi-ion channel.

Authors:  J A Hill; R Coronado; H C Strauss
Journal:  Biophys J       Date:  1989-01       Impact factor: 4.033

7.  The characterization of a monovalent cation-selective channel of mammalian cardiac muscle sarcoplasmic reticulum.

Authors:  B Tomlins; A J Williams; R A Montgomery
Journal:  J Membr Biol       Date:  1984       Impact factor: 1.843

Review 8.  Monovalent ion and calcium ion fluxes in sarcoplasmic reticulum.

Authors:  G Meissner
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

9.  Single chloride-selective channel from cardiac sarcoplasmic reticulum studied in planar lipid bilayers.

Authors:  E Rousseau
Journal:  J Membr Biol       Date:  1989-08       Impact factor: 1.843

10.  Asymmetric block of a monovalent cation-selective channel of rabbit cardiac sarcoplasmic reticulum by succinyl choline.

Authors:  M A Gray; R A Montgomery; A J Williams
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

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