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Research Article Free access | 10.1172/JCI106441
Department of Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
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Department of Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Find articles by Kaminsky, N. in: JCI | PubMed | Google Scholar
Department of Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Find articles by Hardman, J. in: JCI | PubMed | Google Scholar
Department of Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Find articles by Sutherland, E. in: JCI | PubMed | Google Scholar
Department of Physiology, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
Find articles by Liddle, G. in: JCI | PubMed | Google Scholar
Published December 1, 1970 - More info
Kinetic parameters and the renal clearances of plasma adenosine 3′,5′-monophosphate (cyclic AMP) and guanosine 3′,5′-monophosphate (cyclic GMP) were evaluated in normal subjects using tritium-labeled cyclic nucleotides. Each tracer was administered both by single, rapid intravenous injection and by constant intravenous infusion, and the specific activities of the cyclic nucleotides in plasma and urine were determined.
Both cyclic AMP and cyclic GMP were cleared from plasma by glomerular filtration. The kidney was found to add a variable quantity of endogenous cyclic AMP to the tubular urine, amounting to an average of approximately one-third of the total level of cyclic AMP excreted. Plasma was the source of virtually all of the cyclic GMP excreted.
Plasma levels of the cyclic nucleotides appeared to be in dynamic steady state. The apparent volumes of distribution of both nucleotides exceeded extracellular fluid volume, averaging 27 and 38% of body weight for cyclic AMP and cyclic GMP, respectively. Plasma production rates ranged from 9 to 17 nmoles/min for cyclic AMP and from 7 to 13 nmoles/min for cyclic GMP. Plasma clearance rates averaged 668 ml/min for cyclic AMP and 855 ml/min for cyclic GMP. Approximately 85% of the elimination of the cyclic nucleotides from the circulation was due to extrarenal clearance.