Skip Navigation


NDT Advance Access originally published online on May 25, 2008
Nephrology Dialysis Transplantation 2008 23(10):3103-3110; doi:10.1093/ndt/gfn233
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
23/10/3103    most recent
gfn233v2
gfn233v1
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
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Windt, W. A. K. M.
Right arrow Articles by van Dokkum, R. P. E.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Windt, W. A. K. M.
Right arrow Articles by van Dokkum, R. P. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Myocardial infarction does not further impair renal damage in 5/6 nephrectomized rats

Willemijn A. K. M. Windt, Robert H. Henning, Alex C. A. Kluppel, Ying Xu, Dick de Zeeuw and Richard P. E. van Dokkum

Department of Clinical Pharmacology, Groningen Institute for Drug Evaluation (GUIDE), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

Richard P. E. van Dokkum, Department of Clinical Pharmacology, University Medical Center Groningen, PO Box 196, NL-9700 AD, Groningen, The Netherlands. Tel: +31-50-363-2810, Fax: +31-50-363-2812, E-mail: r.p.e.van.dokkum{at}med.umcg.nl



  Abstract

Background. Recent observational studies show that reduced renal function is an independent risk factor for the development of cardiovascular disease. Previously, we reported that myocardial infarction (MI) indeed enhanced mild renal function decline in rats after unilateral nephrectomy (NX) and that RAAS intervention inhibited this decline. The effects of an MI on pre-existing severe renal function loss and the effects of RAAS intervention interrupting this hypothesized cardiorenal interaction are however unknown and clinically even more relevant.

Methods. Male Wistar rats underwent MI, sham MI, 5/6NX, or 5/6NX and MI. Six weeks later, the NX rats were treated with an angiotensin-converting enzyme inhibitor (ACEi) or vehicle for 6 weeks.

Results. An MI did not significantly induce more proteinuria (303 ± 46 versus 265 ± 24 mg/24 h) and glomerulosclerosis (40 ± 11 versus 28 ± 4 arbitrary units) in 5/6NX+MI compared to 5/6NX, and ACEi therapy was equally effective in reducing renal damage in these groups. In the 5/6NX+MI group, decreased renal blood flow and creatinine clearance were observed compared to 5/6NX (2.2 ± 0.6 versus 3.6 ± 0.4 ml/min/kg and 2.1 ± 0.3 versus 2.9 ± 0.3 ml/min/kg), which both increased after ACEi to levels comparable found in the group that underwent 5/6NX alone.

Conclusions. MI does not further deteriorate structural renal damage induced by 5/6NX compared with 5/6NX alone. Furthermore, renal haemodynamic impairment occurs after MI, which can be improved applying ACEi therapy. Therefore, we conclude that treatment with ACEi should be optimized in patients with chronic kidney disease after MI to improve renal function.

Keywords: 5/6 nephrectomy; ACEi therapy; cardiorenal interaction; myocardial infarction

Received for publication: 15. 8.07
Accepted in revised form: 4. 4.08


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.