Literature DB >> 11559770

Phosphate ion channels in sarcoplasmic reticulum of rabbit skeletal muscle.

D R Laver1, G K Lenz, A F Dulhunty.   

Abstract

1. Phosphate ions (P(i)) enter intracellular Ca2+ stores and precipitate Ca2+. Since transport pathways for P(i) across the membrane of intracellular calcium stores have not been identified and anion channels could provide such a pathway, we have examined the P(i) conductance of single anion channels from the sarcoplasmic reticulum (SR) of rabbit skeletal muscle using the lipid bilayer technique. 2. Two anion channels in skeletal muscle SR, the small conductance (SCl) and big conductance (BCl) chloride channels, were both found to have a P(i) conductance of 10 pS in 50 mM P(i). The SCl channel is a divalent anion channel which can pass HPO4(2-) as well as SO4(2-) (60 pS in 100 mM free SO4(2-)). The BCl channel is primarily a monovalent anion channel. The SCl and BCl channels are permeable to a number of small monovalent anions, showing minor selectivity between Cl-, I- and Br- (Cl- > I- > Br-) and relative impermeability to cations and large polyatomic anions (Cs+, Na+, choline+, Tris+, Hepes- and CH3O3S-). 3. The P(i) conductance of SCl and BCl channels suggests that both channel types could sustain the observed P(i) fluxes across the SR membrane. Comparison of the blocking effects of the phosphonocarboxylic acids, ATP and DIDS, on the anion channels with their effects on P(i) transport suggests that the SCl channel is the more likely candidate for the SR P(i) transport mechanism. 4. The SCl channel, with previously unknown function, provides a regulated pathway for P(i) across the SR membrane which would promote P(i) entry and thereby changes in the rapidly releasable Ca2+ store during onset and recovery from muscle fatigue. Anion channels may provide a pathway for P(i) movement into and out of Ca2+ stores in general.

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Year:  2001        PMID: 11559770      PMCID: PMC2278824          DOI: 10.1111/j.1469-7793.2001.t01-1-00715.x

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


  40 in total

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5.  ATP inhibition and rectification of a Ca2+-activated anion channel in sarcoplasmic reticulum of skeletal muscle.

Authors:  G P Ahern; D R Laver
Journal:  Biophys J       Date:  1998-05       Impact factor: 4.033

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7.  Phosphate transport into the sarcoplasmic reticulum of skinned fibres from rat skeletal muscle.

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8.  Regulation of the sarcoplasmic reticulum ryanodine receptor by inorganic phosphate.

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9.  Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle.

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Review 1.  Role of phosphate and calcium stores in muscle fatigue.

Authors:  D G Allen; H Westerblad
Journal:  J Physiol       Date:  2001-11-01       Impact factor: 5.182

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Journal:  Pflugers Arch       Date:  2016-12-21       Impact factor: 3.657

3.  A chloride channel blocker prevents the suppression by inorganic phosphate of the cytosolic calcium signals that control muscle contraction.

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Journal:  J Physiol       Date:  2020-10-19       Impact factor: 5.182

4.  The multiple roles of phosphate in muscle fatigue.

Authors:  David G Allen; Sofie Trajanovska
Journal:  Front Physiol       Date:  2012-12-11       Impact factor: 4.566

Review 5.  Importance of Dietary Phosphorus for Bone Metabolism and Healthy Aging.

Authors:  Juan Serna; Clemens Bergwitz
Journal:  Nutrients       Date:  2020-09-30       Impact factor: 5.717

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