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pubmed-article:8837234pubmed:abstractTextThe present study was undertaken to characterize the export of cGMP from human erythrocytes at 37 degrees C. Inside-out membrane vesicles were exposed to cGMP and [3H]-cGMP in the presence and absence of 2 mmol l-1 ATP. In the absence of ATP, an equilibrium was reached within 15 min for the lowest tested concentration (0.65 mumol l-1), and the amount of cGMP in the vesicles was linearly correlated to the cGMP concentrations in the incubate. These observations suggest that the ATP-independent process represents passive diffusion or non-saturated binding to membrane components. In the presence of ATP, cGMP accumulated linearly during the test period (up to 120 min) and the transport into the inside-out vesicles was dependent on both low- and high-Km transport. The kinetic parameters for the low-Km process were determined after 5 and 120 min, the Km values being 4.6 (SD 1.9) and 4.7 (SD 1.1) mumol l-1 (n = 3), respectively. The corresponding Vmax values were 400 (SD 50) and 440 (SD 70) fmol mg-1 min-1. The high-Km process was characterized by Km = 170 (SD 50) mumol-1 and Vmax = 1610 (SD 280) fmol mg-1 min-1 (n = 5). The present data demonstrate an ATP-requiring saturable transport system for cGMP in human erythrocytes.lld:pubmed
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pubmed-article:8837234pubmed:authorpubmed-author:SagerGGlld:pubmed
pubmed-article:8837234pubmed:authorpubmed-author:KjørstadK EKElld:pubmed
pubmed-article:8837234pubmed:authorpubmed-author:MoriG AGAlld:pubmed
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pubmed-article:8837234pubmed:pagination289-93lld:pubmed
pubmed-article:8837234pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:8837234pubmed:year1996lld:pubmed
pubmed-article:8837234pubmed:articleTitleExport of guanosine 3',5'-cyclic monophosphate (cGMP) from human erythrocytes characterized by inside-out membrane vesicles.lld:pubmed
pubmed-article:8837234pubmed:affiliationDepartment of Pharmacology, University of Tromsø, Norway.lld:pubmed
pubmed-article:8837234pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8837234pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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