Literature DB >> 364994

Quantitative ultrastructural analysis in cardiac membrane physiology.

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Abstract

Quantitative measurements on electron micrographs of heart muscle can yield information useful for cellular physiologists and at present not obtainable in other ways. These methods are subject to preparative artifact, sampling problems, and problems inherent in the mathematical description of ultrastructure. Nevertheless they provide the best available data for membrane areas of the plasmalemma and its components, as well as for membrane areas of the sarcoplasmic reticulum and mitochondria. Morphometric methods can be used to study growth of membranes. Changes in the volumes of intracellular membrane-limited subcompartments can also be measured. Quantitative analysis of freeze-fractured membrane replicas can be carried out either by a statistical approach or by optical diffraction. In this way, physiological perturbations or developmental events leading to changes in membrane permeability can be studied for correlated changes in membrane structure.

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Year:  1978        PMID: 364994     DOI: 10.1152/ajpcell.1978.235.5.C147

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


  77 in total

1.  Low sodium inotropy is accompanied by diastolic Ca2+ gain and systolic loss in isolated guinea-pig ventricular myocytes.

Authors:  W Meme; S O'Neill; D Eisner
Journal:  J Physiol       Date:  2001-02-01       Impact factor: 5.182

2.  Reverse mode of the sarcoplasmic reticulum calcium pump and load-dependent cytosolic calcium decline in voltage-clamped cardiac ventricular myocytes.

Authors:  T R Shannon; K S Ginsburg; D M Bers
Journal:  Biophys J       Date:  2000-01       Impact factor: 4.033

3.  Distribution of proteins implicated in excitation-contraction coupling in rat ventricular myocytes.

Authors:  D R Scriven; P Dan; E D Moore
Journal:  Biophys J       Date:  2000-11       Impact factor: 4.033

4.  A mathematical model of action potential heterogeneity in adult rat left ventricular myocytes.

Authors:  S V Pandit; R B Clark; W R Giles; S S Demir
Journal:  Biophys J       Date:  2001-12       Impact factor: 4.033

5.  Role of the Na(+)-Ca(2+) exchanger as an alternative trigger of CICR in mammalian cardiac myocytes.

Authors:  Chunlei Han; Pasi Tavi; Matti Weckström
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

6.  Relationship between K+ channel down-regulation and [Ca2+]i in rat ventricular myocytes following myocardial infarction.

Authors:  R Kaprielian; A D Wickenden; Z Kassiri; T G Parker; P P Liu; P H Backx
Journal:  J Physiol       Date:  1999-05-15       Impact factor: 5.182

7.  Alterations in action potential profile enhance excitation-contraction coupling in rat cardiac myocytes.

Authors:  R Sah; R J Ramirez; R Kaprielian; P H Backx
Journal:  J Physiol       Date:  2001-05-15       Impact factor: 5.182

Review 8.  Sarcolemmal calcium binding sites in heart: II. Mathematical model for diffusion of calcium released from the sarcoplasmic reticulum into the diadic region.

Authors:  A Peskoff; J A Post; G A Langer
Journal:  J Membr Biol       Date:  1992-07       Impact factor: 1.843

9.  A computational model of cytosolic and mitochondrial [ca] in paced rat ventricular myocytes.

Authors:  Jae Boum Youm; Seong Woo Choi; Chang Han Jang; Hyoung Kyu Kim; Chae Hun Leem; Nari Kim; Jin Han
Journal:  Korean J Physiol Pharmacol       Date:  2011-08-31       Impact factor: 2.016

10.  Estimate of net calcium fluxes and sarcoplasmic reticulum calcium content during systole in rat ventricular myocytes.

Authors:  N Negretti; A Varro; D A Eisner
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

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