Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Richter, E.
Right arrow Articles by Wiessler, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Richter, E.
Right arrow Articles by Wiessler, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1990 Oxford University Press

research-article

Intestinal first-pass metabolism of N-nitrosodibutylamine in vascularly autoperfused jejunal and ileal loops of rats

E. Richter, X.-C. Feng and M. Wiessler 1

Walther Straub-Institut für Pharmakologie und Toxikologie, Ludwig Maximilians-Universitat München Nussbaumstrasse 26, D-8000 Mfinchen 2
1Institut für Toxikologie und Chemotherapic Deutsches Krebsforschungszentrum, Im Neucnheimer Feld 280, D-6900 Heidelberg, FRG

N-Nitrosodi-[1-14C] butylamine (NDBA) has been shown to undergo a high first-pass metabolism in isolated perfused rat small intestinal segments. Metabolites resulting from {omega}-hydroxylation of NDBA, the bladder carcinogens N-nltroso-butyl-(4-hydroxybutyl)amlne (NB4HBA) and N-nltroso-butyl-(3-carboxypropyl)-amine (NB3CPA), accounted for >90% of the total radioactivity absorbed. In the present study using vascularly perfused rat small intestinal segments, the high first-pass metabolism of NDBA could be confirmed under nearin vivo conditions despite the much higher absorption rate. At the end of the 36 min experimental period 70–80% of the dose have been absorbed via the portal blood as opposed to 1–10% of the dose after 2 h in vitro perfusion. {omega}-Hydroxylation was again the most important metabolic pathway. However, the relationship of NB3CPA to NB4HBA was shifted in favor of NB4HBA, indicating a concentration and absorption rate dependency in the further metabolism of NB4HBA to NB3CPA.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.