Xanthine oxidase during human fetal development


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ABSTRACT ABSTRACT: Through oxygen free radical production, xanthine oxidase (XOD, E.C.1.2.3.2) has been implicated in the pathogenesis of postischemic and hyperoxic tissue injuries among


newborn. We measured the activity and evaluated the kinetic characteristics of XOD in human fetal liver, intestine, brain, and myocardium. Both the fetal liver and intestine contain a high


XOD activity through gestation. The activity increases in the liver and decreases in the intestine with advancing gestation. The apparent Km for hypoxanthine is 4.8–5.5 μM in the intestine


throughout gestation and in the liver at term but higher than 30 μM in the liver during the first half of pregnancy. The activity is undetectable both in the fetal brain and myocardium


throughout gestation. Thus, XOD activity is present at least in the liver and intestine to account for the oxidation of hypoxanthine and xanthine. However, direct evidence for adenine


nucleotide catabolism, followed by oxidation of the accumulated hypoxanthine during tissue reoxygenation in the human liver or intestine is not available. SIMILAR CONTENT BEING VIEWED BY


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ARTICLE PDF AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Children's Hospital, University of Helsinki, SF-00290, Finland Kim Vettenranta & Kari O Raivio Authors * Kim Vettenranta


View author publications You can also search for this author inPubMed Google Scholar * Kari O Raivio View author publications You can also search for this author inPubMed Google Scholar


RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Vettenranta, K., Raivio, K. Xanthine Oxidase during Human Fetal Development. _Pediatr Res_ 27, 286–288


(1990). https://doi.org/10.1203/00006450-199003000-00017 Download citation * Received: 30 August 1989 * Accepted: 30 October 1989 * Issue Date: 01 March 1990 * DOI:


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