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Downregulation of 5'-nucleotidase in rabbit heart during coronary underperfusion
Center for Bioengineering, University of Washington, Seattle, Washington 98195 The hydrolysis of AMP to adenosine during acute coronary underperfusion is temporarily beneficial to myocardial survival yet may cause tissue injury during sustained underperfusion because of depletion of adenine nucleoti...
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Published in: | American journal of physiology. Heart and circulatory physiology 1998-02, Vol.274 (2), p.H529-H538 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Center for Bioengineering, University of Washington, Seattle,
Washington 98195
The hydrolysis of AMP to adenosine
during acute coronary underperfusion is temporarily
beneficial to myocardial survival yet may cause tissue injury during
sustained underperfusion because of depletion of adenine nucleotides.
We hypothesized that the enzyme mediating AMP hydrolysis,
5'-nucleotidase (5'-NT), is downregulated during sustained
coronary underperfusion to prevent excessive loss of nucleotides.
Langendorff-perfused rabbit hearts were subjected to two successive,
identical 45-min periods of underperfusion (4-5% of baseline
flow) separated by 20 min of reperfusion. Although coronary venous
lactate efflux was comparable in the two periods, total coronary purine
efflux during the second period of underperfusion was attenuated by
75%. Phosphorus nuclear magnetic resonance data showed that ATP fell
46% in the first period but fell only another 10% in the second
period. Phosphocreatine levels fell comparably (75-78%) during
both periods of underperfusion. Analysis using a mathematical model
describing the kinetics of myocardial energetics revealed that the
combined data set was best described by a lower activity of 5'-NT
(52% decrease in maximal reaction velocity) during the second period
of underperfusion. Additional time course experiments showed that the
decrease in 5'-NT activity was slow in onset, requiring ~20 min
of underperfusion. The decrease in 5'-NT activity during
sustained underperfusion may benefit tissue survival by limiting the
depletion of myocardial adenine nucleotides. In conclusion, at the
onset of coronary underperfusion, there is a high activity of
5'-NT, but later during sustained underperfusion, 5'-NT is
downregulated, resulting in decreased AMP hydrolysis to adenosine.
nucleotides; ischemia; nuclear magnetic resonance; adenosine; phosphoenergetics
Deceased 15 July 1997. |
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ISSN: | 0363-6135 1522-1539 |
DOI: | 10.1152/ajpheart.1998.274.2.h529 |