Absorption and Metabolism of Adenine, Adenosine-5'-Monophosphate, Adenosine and Hypoxanthine by the Isolated Vascularly Perfused Rat Small Intestine

• Published in: The Journal of nutrition Vol. 114; no. 4; pp. 753 - 760
• Main Authors: Salati, Lisa M., Gross, Carol J., Henderson, LaVell M., Savaiano, Dennis A.
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 01.04.1984; American Society for Nutritional Sciences
• Subjects: Absorption; adenine; Adenine - metabolism; adenosine; Adenosine - metabolism; Adenosine Monophosphate - metabolism; AMP; Animals; Biological and medical sciences; Carbon Radioisotopes; Fundamental and applied biological sciences. Psychology; human nutrition; Hypoxanthine; Hypoxanthines - metabolism; intestine; Intestine, Small - metabolism; Intestine. Mesentery; Male; nutrition physiology; Rats; Rats, Inbred Strains; uric acid; Vertebrates: digestive system; adenosine; intestine; AMP; hypoxanthine; uric acid; adenine; Vertebrata; Adenosine; Mammalia; Absorption; Rat; Digestive system; Rodentia; Hypoxanthine; Nucleoside; Metabolism; Small intestine
• ISSN: 0022-3166; 1541-6100
• DOI: 10.1093/jn/114.4.753

Intestinal vascular perfusion and in vivo live animal experiments were conducted in order to evaluate the nature and extent of the intestinal metabolism of adenine, adenosine, adenosine-5′-monophosphate (AMP) and hypoxanthine in the rat. Radiolabeled purine substrates were administered intralumenally. Intestinal contents, tissue and/or portal flow were collected and evaluated for resultant purine metabolites by liquid and paper chromatography and paper electrophoresis. Adenosine, AMP and hypoxanthine were quantitatively metabolized to end products (primarily uric acid) within 15 minutes after administration. In contrast, the metabolism of adenine to uric acid was considerably slower. Up to 20% of the administered adenine was recovered unmetabolized in the portal vasculature. Nonetheless uric acid was the primary metabolite recovered from the portal circulation in the isolated intestine regardless of the purine substrate or concentration administered. Since lumenal inosine concentrations rose sharply with increasing doses of AMP, either transport or metabolism of inosine is a rate-limiting step in the intestinal metabolism of purines to uric acid in the rat. Finally, the large percentage of the radiolabel in uric acid recovered in the lumen is consistent with the hypothesis that the intestine is an extrarenal site for purine excretion.