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Prolonged exposure to inositol 1,4,5-trisphosphate does not cause intrinsic desensitization of the intracellular Ca super(2+)-mobilizing receptor
Here we have overloaded the intracellular Ca super(2+) stores of permeabilized rat hepatocytes by incubating them with ATP and super(45)Ca super(2+) in the presence of pyrophosphate, which precipitates Ca super(2+) within the lumen of the stores. Subsequent ATP removal initiated slow super(45)Ca sup...
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Published in: | The Journal of biological chemistry 1992-01, Vol.267 (23), p.16312-16316 |
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container_end_page | 16316 |
container_issue | 23 |
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container_title | The Journal of biological chemistry |
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creator | Oldershaw, KA Richardson, A Taylor, C W |
description | Here we have overloaded the intracellular Ca super(2+) stores of permeabilized rat hepatocytes by incubating them with ATP and super(45)Ca super(2+) in the presence of pyrophosphate, which precipitates Ca super(2+) within the lumen of the stores. Subsequent ATP removal initiated slow super(45)Ca super(2+) efflux that followed zero-order kinetics, allowing us to examine the effects of InsP sub(3) over a prolonged time course. InsP sub(3) produced a concentration-dependent increase in the super(45)Ca super(2+) efflux rate that was sustained for several min. The rate rapidly returned to the unstimulated level after the addition of decavanadate, a competitive antagonist of InsP sub(3) at its receptor. Prior incubation with a submaximal concentration of InsP sub(3) (1 mu M) did not affect the subsequent enhanced rate of super(45)Ca super(2+) efflux stimulated by a higher, but still submaximal, concentration of InsP sub(3) (3 mu M). |
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Subsequent ATP removal initiated slow super(45)Ca super(2+) efflux that followed zero-order kinetics, allowing us to examine the effects of InsP sub(3) over a prolonged time course. InsP sub(3) produced a concentration-dependent increase in the super(45)Ca super(2+) efflux rate that was sustained for several min. The rate rapidly returned to the unstimulated level after the addition of decavanadate, a competitive antagonist of InsP sub(3) at its receptor. Prior incubation with a submaximal concentration of InsP sub(3) (1 mu M) did not affect the subsequent enhanced rate of super(45)Ca super(2+) efflux stimulated by a higher, but still submaximal, concentration of InsP sub(3) (3 mu M).</abstract></addata></record> |
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subjects | calcium effects on exposure hepatocytes inositol 1,4,5-trisphosphate receptors |
title | Prolonged exposure to inositol 1,4,5-trisphosphate does not cause intrinsic desensitization of the intracellular Ca super(2+)-mobilizing receptor |
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