AJP - GI Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 295: G1104-G1110, 2008. First published October 2, 2008; doi:10.1152/ajpgi.90374.2008
0193-1857/08 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
295/5/G1104    most recent
90374.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Haenisch, B.
Right arrow Articles by Molderings, G. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Haenisch, B.
Right arrow Articles by Molderings, G. J.

HORMONES AND SIGNALING

Regulatory mechanisms underlying agmatine homeostasis in humans

Britta Haenisch,1 Ivar von Kügelgen,1 Heinz Bönisch,1 Manfred Göthert,1 Tilman Sauerbruch,2 Michael Schepke,2 Günter Marklein,3 Katja Höfling,3 Detlev Schröder,4 and Gerhard J. Molderings5

1Department of Pharmacology and Toxicology and 3Institute for Medical Microbiology, Immunology and Parasitology, University of Bonn; 2Department of Internal Medicine I and 5Institute of Human Genetics, University Hospital of Bonn; 4Department of Surgery, Evangelische Kliniken Bonn, Betriebsstätte Waldkrankenhaus, Bonn, Germany

Submitted 12 June 2008 ; accepted in final form 25 September 2008

Regulation of agmatine homeostasis has so far only been poorly defined. In the present study, three mechanisms regulating human agmatine homeostasis were investigated. 1) Enzymatic regulation: expression of arginine decarboxylase, diamine oxidase, and ornithine decarboxylase in human colon neoplastic tissue was, at the mRNA level, about 75% and 50% lower and 150% higher, respectively, than in the adjacent normal tissue; expression of agmatinase was unchanged. 2) Bacteria-derived agmatine: ten representative bacteria strains of the human intestinal microbiota considerably differed in agmatine production and its efflux into their surrounding fluid, suggesting that the composition of the intestinal microbiota influences the agmatine availability in the gut lumen for absorption. 3) Regulation of blood plasma agmatine concentration by the human liver: at low concentrations in portal venous blood plasma, agmatine either slightly increased or further decreased in blood plasma through liver passage. Above a threshold of 14 ng/ml agmatine in the portal venous blood plasma, substantial hepatic agmatine removal from blood occurred. Taken together, a perturbation of agmatine homeostasis has been proven to be involved in the regulation of malignant cell proliferation. The amount of agmatine available for absorption, which is an important physiological source of agmatine in the human organism, should differ considerably depending on the composition of the bacterial flora in the chyme since the various species of intestinal bacteria largely differ in their ability to form agmatine. Finally, evidence has been presented that the liver plays a crucial physiological role in the maintenance of agmatine homeostasis in the human organism.

intestinal bacterial microflora; colon cancer; arginine decarboxylase; liver cirrhosis; hepatic agmatine uptake



Address for reprint requests and other correspondence: G. Molderings, Inst. of Human Genetics, Univ. Hospital of Bonn, Wilhelmstrasse 31, D-53111 Bonn, Germany (e-mail: molderings{at}uni-bonn.de)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2008 by the American Physiological Society.