Physiol. Genomics Information on EB 2010
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics (September 16, 2008). doi:10.1152/physiolgenomics.00187.2007
This Article
Right arrow Full Text (PDF)
Right arrow Supplemental Figures and Tables
Right arrow All Versions of this Article:
35/3/330    most recent
00187.2007v1
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ochiai, Y.
Right arrow Articles by Kato, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ochiai, Y.
Right arrow Articles by Kato, N.
Submitted on August 14, 2007
Accepted on September 14, 2008

Dynamic Changes of the Renin-Angiotensin and Associated Systems in the Rat After Pharmacological and Dietary Interventions in vivo

Yoshinori Ochiai1, Yi-Qiang Liang1, Masakuni Serizawa1, and Norihiro Kato1*

1 Department of Gene Diagnostics and Therapeutics, Research Institute, International Medical Center of Japan, Tokyo, Japan

* To whom correspondence should be addressed. E-mail: nokato{at}ri.imcj.go.jp.

To address the multiplicity of the renin-angiotensin system (RAS) with particular interest in its local, synergistic regulation, we investigate dynamic changes of the RAS and associated systems in response to external stimuli in the rat. We tested influences of the RAS blockade (candesartan and enalapril), diuretics (hydrochlorothiazide), high lipid diet and salt loading on tissue mRNA expression of 12 principal genes. Under the hemodynamic conditions appropriately pre-determined, we quantitatively evaluated mRNA expression changes with and without each intervention in 5 organs — the brain, heart, kidney, liver and adipose tissues — of male rats (n=5 each). A total of 250 tissues were examined by real-time PCR. Significant changes in mRNA expression (P <0.05) were found in a drug-, diet- and tissue-specific manner. For instance, 29% of genes (14 out of 48 tissues showing detectable mRNA expression levels) were differentially regulated by candesartan and enalapril, although both drugs reduced blood pressure to similar extents. When the overall interactions among 12 genes were compared between interventions, the RAS and associated systems appeared to change in the opposite direction between candesartan and high lipid diet in the adipose tissue and between candesartan and salt loading in the heart. Enalapril, however, induced unique patterns of perturbation in the local RAS under the corresponding conditions. Thus, this study provides a fundamental picture of gene expression profile in vivo in the RAS and associated systems. In particular, our data highlight differential regulation between candesartan and enalapril, which may reflect the individual pharmacological properties regarding clinical implications.







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