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Calcium Distribution and Exchange in the Rat Uterus
The calcium content and distribution of the rat uterus were determined employing flame photometry and Ca(45) determinations. The total uterine calcium concentration was found to be 2.25 millimoles (mmoles) per kilogram wet weight, 0.45 of which was inexchangeable. The exchangeable Ca could be divide...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1966
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328326/ https://www.ncbi.nlm.nih.gov/pubmed/5924111 http://dx.doi.org/10.1085/jgp.0491265 |
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author | van BREEMEN, CASEY DANIEL, E. E. van BREEMEN, DIANNE |
author_facet | van BREEMEN, CASEY DANIEL, E. E. van BREEMEN, DIANNE |
author_sort | van BREEMEN, CASEY |
collection | PubMed |
description | The calcium content and distribution of the rat uterus were determined employing flame photometry and Ca(45) determinations. The total uterine calcium concentration was found to be 2.25 millimoles (mmoles) per kilogram wet weight, 0.45 of which was inexchangeable. The exchangeable Ca could be divided into 0.8 mmole/kg wet weight extracellular and 1.0 mmole/kg wet weight intracellular. The concentration of ionic Ca in rat serum was obtained by equilibrium dialysis as 1.5 mM or 53 % of the total serum Ca. The observed Ca distribution required that its active transport be postulated, since the membrane was shown to be permeable to Ca and the internal Ca concentration was far below its electrochemical equilibrium value. Metabolic inhibition by iodoacetate or dinitrophenol caused a net Ca uptake, but cooling to 4°C and ouabain did not. Iodoacetate did not affect the Ca(45) efflux, but did increase the influx, suggesting that active Ca transport is accomplished by an exclusion mechanism. In experiments with varied external sodium concentrations, no evidence was obtained that sodium competes with calcium for inward transport. Cellular Ca binding was measured under conditions of prolonged metabolic inhibition, which abolished both active transport and the membrane potential. The association constants obtained were compatible with intracellular Ca binding to proteins, but insufficient to account for the low level of intracellular ionic Ca believed essential for relaxation. Hence metabolically dependent intracellular Ca binding was postulated. The Ca(45) efflux was slowed down by Ca-free efflux media. The presence of Sr or EDTA could completely prevent this decrease in efflux rate, and Ba could partly prevent it. Changes in Mg and Na concentration did not affect the rate of Ca(45) efflux. A model to explain Ca exchange across smooth muscle membranes has been proposed. |
format | Online Article Text |
id | pubmed-3328326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1966 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33283262012-04-23 Calcium Distribution and Exchange in the Rat Uterus van BREEMEN, CASEY DANIEL, E. E. van BREEMEN, DIANNE J Gen Physiol Articles The calcium content and distribution of the rat uterus were determined employing flame photometry and Ca(45) determinations. The total uterine calcium concentration was found to be 2.25 millimoles (mmoles) per kilogram wet weight, 0.45 of which was inexchangeable. The exchangeable Ca could be divided into 0.8 mmole/kg wet weight extracellular and 1.0 mmole/kg wet weight intracellular. The concentration of ionic Ca in rat serum was obtained by equilibrium dialysis as 1.5 mM or 53 % of the total serum Ca. The observed Ca distribution required that its active transport be postulated, since the membrane was shown to be permeable to Ca and the internal Ca concentration was far below its electrochemical equilibrium value. Metabolic inhibition by iodoacetate or dinitrophenol caused a net Ca uptake, but cooling to 4°C and ouabain did not. Iodoacetate did not affect the Ca(45) efflux, but did increase the influx, suggesting that active Ca transport is accomplished by an exclusion mechanism. In experiments with varied external sodium concentrations, no evidence was obtained that sodium competes with calcium for inward transport. Cellular Ca binding was measured under conditions of prolonged metabolic inhibition, which abolished both active transport and the membrane potential. The association constants obtained were compatible with intracellular Ca binding to proteins, but insufficient to account for the low level of intracellular ionic Ca believed essential for relaxation. Hence metabolically dependent intracellular Ca binding was postulated. The Ca(45) efflux was slowed down by Ca-free efflux media. The presence of Sr or EDTA could completely prevent this decrease in efflux rate, and Ba could partly prevent it. Changes in Mg and Na concentration did not affect the rate of Ca(45) efflux. A model to explain Ca exchange across smooth muscle membranes has been proposed. The Rockefeller University Press 1966-07-01 /pmc/articles/PMC3328326/ /pubmed/5924111 http://dx.doi.org/10.1085/jgp.0491265 Text en © 1966 Chowdhury and Chanda This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles van BREEMEN, CASEY DANIEL, E. E. van BREEMEN, DIANNE Calcium Distribution and Exchange in the Rat Uterus |
title | Calcium Distribution and Exchange in the Rat Uterus |
title_full | Calcium Distribution and Exchange in the Rat Uterus |
title_fullStr | Calcium Distribution and Exchange in the Rat Uterus |
title_full_unstemmed | Calcium Distribution and Exchange in the Rat Uterus |
title_short | Calcium Distribution and Exchange in the Rat Uterus |
title_sort | calcium distribution and exchange in the rat uterus |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328326/ https://www.ncbi.nlm.nih.gov/pubmed/5924111 http://dx.doi.org/10.1085/jgp.0491265 |
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