rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
1989-8-29
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pubmed:abstractText |
The recently developed method of loading isolated heart mitochondria with the fluorescent pH indicator, BCECF, was applied to monitor the Na+o/H+i exchange process from the matrix side of the membrane. The Na+-induced changes in the pH of the matrix (pHm) showed that: (i) the Na+o/H+i exchange followed Michaelis-Menten kinetics with respect to external Na+ with a Km of approx. 20 mM; (ii) in contrast to this, the dependence of the exchange rate on the matrix [H+] did not obey the Michaelian model. No Na+-induced alkalinization occurred above a pHm of 7.45 +/- 0.09 (n = 4). Below this value the reciprocal of the transport rate and that of the matrix [H+] deviated upwardly from the straight line. The results suggest that internal H+ might exert allosteric control on the mitochondrial Na+/H+ exchange process.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
0014-5793
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
17
|
pubmed:volume |
251
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
49-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2546827-Animals,
pubmed-meshheading:2546827-Antimycin A,
pubmed-meshheading:2546827-Biological Transport,
pubmed-meshheading:2546827-Carrier Proteins,
pubmed-meshheading:2546827-Fluoresceins,
pubmed-meshheading:2546827-Fluorescent Dyes,
pubmed-meshheading:2546827-Hydrogen-Ion Concentration,
pubmed-meshheading:2546827-Intracellular Membranes,
pubmed-meshheading:2546827-Kinetics,
pubmed-meshheading:2546827-Membrane Potentials,
pubmed-meshheading:2546827-Mitochondria, Heart,
pubmed-meshheading:2546827-Protons,
pubmed-meshheading:2546827-Rats,
pubmed-meshheading:2546827-Sodium,
pubmed-meshheading:2546827-Sodium-Hydrogen Antiporter,
pubmed-meshheading:2546827-Spectrometry, Fluorescence
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pubmed:year |
1989
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pubmed:articleTitle |
Na+/H+ exchange in mitochondria as monitored by BCECF fluorescence.
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pubmed:affiliation |
Department of Physiology, Semmelweis University of Medicine, Budapest, Hungary.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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