pubmed-article:8394428 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0014792 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C1383501 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0001476 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0021467 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0596235 | lld:lifeskim |
pubmed-article:8394428 | lifeskim:mentions | umls-concept:C0205266 | lld:lifeskim |
pubmed-article:8394428 | pubmed:dateCreated | 1993-9-13 | lld:pubmed |
pubmed-article:8394428 | pubmed:abstractText | 1. The inhibitory effect of high intracellular calcium on the saturated Ca2+ efflux through the Ca2+ pump (Vmax) was investigated in intact human red cells. Cells were loaded with Ca2+ by exposure to the calcium ionophore A23187, at different external Ca2+ concentrations ([Ca2+]o). Ca2+ extrusion by the pump was followed after either ionophore removal or Co2+ addition. 2. fifty per cent inhibition of Vmax was obtained with total intracellular calcium ([CaT]i) of approximately 3 mmol/l cells. For any given initial Ca2+ load, Vmax showed no tendency to increase as [CaT]i was progressively reduced during Ca2+ efflux. This suggests that the pump Vmax was determined by the magnitude of the initial [Ca2+]i. 3. To estimate [Ca2+]i from [CaT]i in Co(2+)-loaded cells, the possible competition between Co2+ and Ca2+ for the known cytoplasmic Ca2+ buffers (alpha-buffers) was investigated first. Comparison between Ca2+ efflux after either Co2+ exposure or ionophore wash-out showed that the efflux patterns were essentially identical, down to the lowest measurable [CaT]i. This indicates that Co2+ does not compete with Ca2+ for the alpha-buffers. Hence, since [Ca2+]i = alpha [CaT]i, and alpha approximately 0.15-0.35, the initial [Ca2+]i load for 50% Vmax inhibition was between 0.4 and 1.1 mM. 4. Ancillary new findings demonstrated that, unlike the situation with alpha-buffers, Co2+ displaced Ca2+ from the cell-incorporated calcium chelator benz-2, and that benz-2 incorporation had no effect on Co(2+)-exposed Ca2+ pump desaturation. This validates the use of benz-2 to study Ca2+ pump kinetics in intact cells. | lld:pubmed |
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pubmed-article:8394428 | pubmed:language | eng | lld:pubmed |
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pubmed-article:8394428 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:8394428 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8394428 | pubmed:month | Feb | lld:pubmed |
pubmed-article:8394428 | pubmed:issn | 0022-3751 | lld:pubmed |
pubmed-article:8394428 | pubmed:author | pubmed-author:TiffertTT | lld:pubmed |
pubmed-article:8394428 | pubmed:author | pubmed-author:LewV LVL | lld:pubmed |
pubmed-article:8394428 | pubmed:author | pubmed-author:PereiraA CAC | lld:pubmed |
pubmed-article:8394428 | pubmed:author | pubmed-author:SamellasDD | lld:pubmed |
pubmed-article:8394428 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8394428 | pubmed:volume | 461 | lld:pubmed |
pubmed-article:8394428 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8394428 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8394428 | pubmed:pagination | 63-73 | lld:pubmed |
pubmed-article:8394428 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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pubmed-article:8394428 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:8394428 | pubmed:articleTitle | Inhibition of the calcium pump by high cytosolic Ca2+ in intact human red blood cells. | lld:pubmed |
pubmed-article:8394428 | pubmed:affiliation | Physiological Laboratory, University of Cambridge. | lld:pubmed |
pubmed-article:8394428 | pubmed:publicationType | Journal Article | lld:pubmed |
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